WO2004113913A1 - Method for analyte measurement employing maximum dosing time delay - Google Patents

Method for analyte measurement employing maximum dosing time delay Download PDF

Info

Publication number
WO2004113913A1
WO2004113913A1 PCT/US2004/019627 US2004019627W WO2004113913A1 WO 2004113913 A1 WO2004113913 A1 WO 2004113913A1 US 2004019627 W US2004019627 W US 2004019627W WO 2004113913 A1 WO2004113913 A1 WO 2004113913A1
Authority
WO
WIPO (PCT)
Prior art keywords
electrodes
measurement
test
sample
response
Prior art date
Application number
PCT/US2004/019627
Other languages
French (fr)
Inventor
David W. Burke
Lance S. Kuhn
Original Assignee
Roche Diagnostics Gmbh
F.Hoffmann-La Roche Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Roche Diagnostics Gmbh, F.Hoffmann-La Roche Ag filed Critical Roche Diagnostics Gmbh
Publication of WO2004113913A1 publication Critical patent/WO2004113913A1/en

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/28Electrolytic cell components
    • G01N27/30Electrodes, e.g. test electrodes; Half-cells
    • G01N27/327Biochemical electrodes, e.g. electrical or mechanical details for in vitro measurements
    • G01N27/3271Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood
    • G01N27/3273Devices therefor, e.g. test element readers, circuitry
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/28Electrolytic cell components
    • G01N27/30Electrodes, e.g. test electrodes; Half-cells
    • G01N27/327Biochemical electrodes, e.g. electrical or mechanical details for in vitro measurements
    • G01N27/3271Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood
    • G01N27/3274Corrective measures, e.g. error detection, compensation for temperature or hematocrit, calibration

Definitions

  • the present invention relates to a measurement method and apparatus for use in measuring concentrations of an analyte in a fluid.
  • the invention relates more particularly, but not exclusively, to a method and apparatus which may be 15 used for measuring the concentration of glucose in blood.
  • Measuring the concentration of substances, particularly in the presence of 20 other, confounding substances, is important in many fields, and especially in medical diagnosis.
  • the measurement of glucose in body fluids, such as blood is crucial to the effective treatment of diabetes.
  • Diabetic therapy typically involves two types of insulin treatment: basal, and meal-time.
  • Basal insulin refers to continuous, e.g. time-released insulin, often 25 taken before bed.
  • Meal-time insulin treatment provides additional doses of faster acting insulin to regulate fluctuations in blood glucose caused by a variety of factors, including the metabolization of sugars and carbohydrates.
  • Proper regulation of blood glucose fluctuations requires accurate measurement of the concentration of glucose in the blood. Failure to do so can produce extreme 30 complications, including blindness and loss of circulation in the extremities, which can ultimately deprive the diabetic of use of his or her fingers, hands, feet, etc.
  • Multiple methods are known for measuring the concentration of analytes in a blood sample, such as, for example, glucose. Such methods typically fall into one of two categories: optical methods and electrochemical methods.
  • Optical methods generally involve reflectance or absorbance spectroscopy to observe the spectrum shift in a reagent. Such shifts are caused by a chemical reaction that produces a color change indicative of the concentration of the analyte.
  • Electrochemical methods generally involve, alternatively, amperometric or coulometric responses indicative of the concentration of the analyte. See, for example, U.S. Patent Nos.
  • the geometry of the blood sample is typically controlled by a sample- receiving portion of the testing apparatus.
  • the blood sample is typically placed onto a disposable test strip that plugs into the meter.
  • the test strip may have a sample chamber (capillary fill space) to define the geometry of the sample.
  • the effects of sample geometry may be limited by assuring an effectively infinite sample size.
  • the electrodes used for measuring the analyte may be spaced closely enough so that a drop of blood on the test strip extends substantially beyond the electrodes in all directions. Ensuring adequate coverage of the measurement electrodes by the sample, however, is an important factor in achieving accurate test results. This has proven to be problematic in the past, particularly with the use of capillary fill spaces.
  • hematocrit concentration of red blood cells
  • concentration of other chemicals in the blood can effect the signal generation of a blood sample.
  • Variations in the temperature of blood samples is yet another example of a confounding variable in measuring blood chemistry.
  • a system and method are needed that accurately measure blood glucose, even in the presence of confounding variables, including variations in temperature, hematocrit, and the concentrations of other chemicals in the blood.
  • a system and method are also needed to ensure adequate coverage of the measurement electrodes by the sample, particularly in capillary fill devices.
  • a system and method are likewise needed that accurately measure an analyte in a fluid. It is an object of the present invention to provide such a system and method.
  • a method of performing a measurement on a biological fluid in a test strip comprising: providing a biological fluid test strip including a capillary fill chamber extending a length along the test strip from an intake opening to a terminus, a first pair of electrodes in operative communication with the chamber, and a second pair of electrodes in operative communication with the chamber; dosing the test strip with a biological fluid effective to cause the biological fluid to flow from the intake opening toward the terminus; applying a first test signal to one of the first pair of electrodes; measuring a first response to the first test signal at the other of the first pair of electrodes; maintaining the first pair of electrodes in an inoperative state upon the measuring the first response; applying a second test signal to one of the second pair of electrodes; measuring a second response to the second test signal at the other of the second pair of electrodes; and performing a measurement upon the biological fluid after the measuring the second response.
  • a method of indicating acceptable fill time of a biological fluid in a test strip comprising: providing a biological fluid test strip including a capillary fill chamber extending a length along the test strip from an intake opening to a terminus, a first pair of electrodes in operative communication with the chamber, and a second pair of electrodes in operative communication with the chamber; dosing the test strip with a biological fluid effective to cause the biological fluid to flow from the intake opening toward the terminus; flowing a biological fluid from the opening toward the terminus; first determining when the biological fluid contacts the first electrodes; second determining when the biological fluid contacts the second electrodes; determining a fill time value based upon the first determining and the second determining; and comparing the fill time value to a predetermined value.
  • Fig. 1 is a diagram of a first embodiment excitation signal suitable for use in a system and method according to the present invention, having a serially-applied AC component and DC component.
  • Fig. 2 is a diagram of a second embodiment excitation signal suitable for use in a system and method according to the present invention, having a simultaneously-applied AC component and DC component.
  • Figs. 3A-B illustrate a first embodiment test strip of the present invention.
  • Fig. 4 is a diagram of an excitation signal utilized in the test of Example 1.
  • Fig. 5 is a plot of the correlation coefficient r 2 (glucose vs. DC current) versus Read Time for the test of Example 1 with no incubation time.
  • Fig. 6 is a plot of the correlation coefficient r 2 (glucose vs. DC current) versus Read Time for the test of Example 1 with varying incubation time.
  • Fig. 7 is a plot of AC admittance versus hematocrit for the test of Example 2.
  • Fig. 8 is a plot of uncompensated DC current versus glucose for the test of Example 2.
  • Fig. 9 is a plot of the predicted glucose response versus the actual glucose response for the test of Example 2.
  • Fig. 10 is a diagram of an excitation signal utilized in the test of Example 3.
  • Fig. 11 is a plot of the AC phase angle versus reference glucose for the test of Example 3.
  • Fig. 12 is a plot of the predicted glucose response versus the actual glucose response for the test of Example 3.
  • Fig. 13 is a diagram of an excitation signal utilized in the test of Example 4.
  • Fig. 14 is a plot of AC admittance versus hematocrit (parametrically displayed with temperature) for the test of Example 4.
  • Fig. 15 is a plot of the uncompensated DC response versus actual glucose for the test of Example 4.
  • Fig. 16 is a plot of the predicted glucose response versus actual glucose response for the test of Example 4.
  • Figs. 17A-B illustrate a second embodiment test strip of the present invention.
  • Fig. 18 is a plot parametrically illustrating the correlation coefficient r 2 between the DC current response and glucose level as Read Time varies for three combinations of temperature and hematocrit in the test of Example 5.
  • Fig. 19 is a diagram of the excitation signal utilized in the test of Example 5.
  • Fig. 20 is a plot of AC admittance versus hematocrit as temperature is parametrically varied in the test of Example 5.
  • Fig. 21 is a plot of AC admittance phase angle versus hematocrit as temperature is parametrically varied in the test of Example 5.
  • Fig. 22 is a plot of the uncompensated DC response versus actual glucose for the test of Example 5.
  • Fig. 23 is a plot of the predicted glucose response versus actual glucose response for the test of Example 5.
  • Fig. 24 is a diagram of the excitation signal utilized in the test of Example 6.
  • Fig. 25 is a plot of the correlation coefficient r 2 between hematocrit and DC response current plotted against hematocrit in the test of Example 6.
  • Fig. 26 is a plot of AC admittance phase angle versus hematocrit for the test of Example 6.
  • Fig. 27 is a plot of the uncompensated DC response versus actual glucose for the test of Example 6.
  • Fig. 28 is a plot of the compensated DC response versus actual glucose for a 1.1 second Total Test Time of Example 6.
  • Fig. 29 is a plot of the compensated DC response versus actual glucose for a 1.5 second Total Test Time of Example 6.
  • Fig. 30 is a plot of the compensated DC response versus actual glucose for a 1.9 second Total Test Time of Example 6.
  • Fig. 31 is a table detailing the heights and widths of the capillary fill channels used in the test devices of Example 8, as well as schematic diagrams of convex and concave sample flow fronts in a capillary fill space.
  • Figs. 32A-C are schematic plan views of a test strip illustrating the potential for biased measurement results when a concave flow front encounters a prior art dose sufficiency electrode.
  • Fig. 33 is a schematic plan view of a test strip of the present invention having a pair of perpendicular dose sufficiency electrodes that are independent from the measurement electrodes.
  • Figs. 34A-B are schematic plan views of the test strip of FIG. 33 containing samples with convex and concave flow fronts, respectively.
  • Figs. 35A-B are schematic plan views of a test strip of the present invention having a pair of parallel dose sufficiency electrodes that are independent from the measurement electrodes.
  • Fig. 36 is a schematic plan view of the test strip of Fig. 35, schematically illustrating the electric field lines that communicate between the electrode gap when the electrodes are covered with sample.
  • a system and method according to the present invention permit the accurate measurement of an analyte in a fluid.
  • the measurement of the analyte remains accurate despite the presence of interferants, which would otherwise cause error.
  • a blood glucose meter according to the present invention measures the concentration of blood glucose without error that is typically caused by variations in the temperature and the hematocrit level of the sample.
  • the accurate measurement of blood glucose is invaluable to the prevention of blindness, loss of circulation, and other complications of inadequate regulation of blood glucose in diabetics.
  • An additional advantage of a system and method according to the present invention is that measurements can be made much more rapidly and with much smaller sample volumes, making it more convenient for the diabetic person to measure their blood glucose.
  • accurate and rapid measurement of other analytes in blood, urine, or other biological fluids provides for improved diagnosis and treatment of a wide range of medical conditions.
  • electrochemical blood glucose meters typically (but not always) measure the electrochemical response of a blood sample in the presence of a reagent.
  • the reagent reacts with the glucose to produce charge carriers that are not otherwise present in blood. Consequently, the electrochemical response of the blood in the presence of a given signal is intended to be primarily dependent upon the concentration of blood glucose.
  • the electrochemical response of the blood to a given signal is dependent upon other factors, including hematocrit and temperature. See, for example, U.S. Patents Nos.
  • a preferred embodiment system and method for measuring blood glucose according to the present invention operates generally by using the signal- dependence of the contribution of various factors to the impedance (from which admittance and phase angle may be derived) of a blood sample. Because the contribution of various factors to the impedance of a blood sample is a function of the applied signal, the effects of confounding factors (that is, those other than the factors sought to be measured) can be substantially reduced by measuring the impedance of the blood sample to multiple signals. In particular, the effects of confounding factors, (primarily temperature and hematocrit, but also including chemical interferants such as oxygen), contribute primarily to the resistivity of the sample, while the glucose-dependent reaction contributes primarily to the capacitance.
  • confounding factors primarily temperature and hematocrit, but also including chemical interferants such as oxygen
  • the effects of the confounding factors can be eliminated by measuring the impedance of the blood sample to an AC excitation, either alone or in combination with a DC excitation.
  • the impedance (or the impedance derived admittance and phase information) of the AC signal is then used to correct the DC signal or AC derived capacitance for the effects of interferants. It will be appreciated that measurements at sufficiently high AC frequencies are relatively insensitive to the capacitive component of the sample's impedance, while low frequency (including DC) measurements are increasingly (with decreasing frequency) sensitive to both the resistive and the capacitive components of the sample's impedance. The resistive and capacitive components of the impedance can be better isolated by measuring the impedance at a larger number of frequencies.
  • the impedance may be measured at greater than ten frequencies, but preferably at between two and ten frequencies, and most preferably at between two and five frequencies.
  • a signal having an AC component refers to a signal which has some alternating potential (voltage) portions.
  • the signal may be an "AC signal” having 100% alternating potential (voltage) and no DC portions; the signal may have AC and DC portions separated in time; or the signal may be AC with a DC offset (AC and DC signals superimposed).
  • Figure 1 illustrates a preferred embodiment excitation signal suitable for use in a system and method according to the present invention, indicated generally at 100, in which DC excitation and four frequencies of AC excitation are used.
  • Figure 1 also illustrates a typical response to the excitation when the excitation is applied to a sample of whole blood mixed with an appropriate reagent, the response indicated generally at 102.
  • a relatively high frequency signal is applied, starting at time 101.
  • the frequency is between about lOkHz and about 20kHz, and has an amplitude between about 12.4mV and about 56.6mV.
  • a frequency of 20kHz is used in the example of FIG. 1.
  • Those skilled in the art will appreciate that these values may be optimised to various parameters such as cell geometry and the particular cell chemistry.
  • a test strip is inserted into the meter and several possible responses to the insertion of the test strip into the glucose meter are shown.
  • the test strip may also be inserted before the excitation signal 100 is initiated (i.e. before time 101); however, the test strip itself may advantageously be tested as a control for the suitability of the strip. It is therefore desirable that the excitation signal 100 be initiated prior to test strip insertion.
  • relatively large current leakage as shown at 112 may occur if the strip is wet, either because the test strip was pre-dosed, or due to environmental moisture. If the test strip has been pre-dosed and permitted to largely or completely dry out, an intermediate current leakage may occur, as shown at 114.
  • insertion of the test strip will cause no or negligible leakage current due to an expected absence of charge carriers between the test electrodes, as shown at 116.
  • Measured current leakage above a predetermined threshold level will preferably cause an error message to be displayed and prevent the test from continuing.
  • the user doses the strip, as shown at time 120. While the blood sample is covering the electrodes the current response will rapidly increase, as the glucose reacts with the reagent and the contact area increases to maximum. The response current will reach a stable state, which indicates the impedance of the sample at this frequency.
  • the excitation frequency is then stepped down to about 10kHz in the preferred embodiment, as shown at time 130.
  • Another measurement is made and recorded by the test meter, and the frequency is stepped down to about 2kHz in the preferred embodiment, as shown at 140.
  • a third measurement is made and recorded by the test meter at this frequency.
  • a fourth measurement is made at about 1kHz in the preferred embodiment, as shown at 150.
  • measurements are taken at regular intervals (e.g. 10 points per cycle).
  • the stable state response may be measured as current or voltage (preferably both magnitude and phase) and the impedance and/or admittance can be calculated therefrom.
  • the present specification and claims may refer alternately to the AC response as impedance or admittance (magnitude and/or phase), resistance, conductivity, current or charge, and to the DC response as current, charge, resistance or conductivity, those skilled in the art will recognize that these measures are interchangeable, it only being necessary to adjust the measurement and correction mathematics to account for which measure is being employed.
  • the test meter applies a voltage to one electrode and measures the current response at the other electrode to obtain both the AC and DC response.
  • measurements are made at fewer or more frequencies.
  • measurements are made at at least two AC frequencies at least an order of magnitude apart. If more than two AC frequencies are used, then it is preferable that the highest and lowest frequencies be at least an order of magnitude apart.
  • AC signal may be used in an AC signal, including, for example, sinusoidal, trapezoidal, triangle, square and filtered square.
  • the AC signal has a filtered square waveform that approximates a sine wave. This waveform can be generated more economically than a true sine wave, using a square wave generator and one or more filters.
  • the signal is preferably briefly reduced to zero amplitude, as shown at 160.
  • the DC excitation is then begun, as shown at 170.
  • the amplitude of the DC excitation is advantageously selected based on the reagent being used, in order to maximise the resulting response or response robustness. For example, if ferricyanide is being used in a biamperometry system, the DC amplitude is preferably about 300mV. For another example, if a nitrosoaniline derivative is being used in a biamperometry system, the DC amplitude is preferably about 500-550mV.
  • the DC applitude is preferably 600 mV (versus the silver/silver chloride reference electrode) for ferricyanide, and 40-100 mV (versus the silver/silver chloride reference electrode) for nitrosoaniline derivative.
  • measurements are preferably made at a rate of 100 pts/sec.
  • the current response will follow a decay curve (known as a Cottrell curve), as the reaction is limited by the diffusion of unreacted glucose next to the working electrode.
  • the resulting stable-state amplitude (measured or projected) is used to determine a glucose estimation of the sample, as is known in the art.
  • a corrected estimation is then determined that corresponds more closely to the concentration of glucose in the blood, by using the impedance of the sample to the AC signal to correct for the effects of interferants, as explained in greater detail hereinbelow.
  • a method according to the present invention may also be used to measure the concentration of other analytes and in other fluids.
  • a method according to the present invention may be used to measure the concentration of a medically significant analyte in urine, saliva, spinal fluid, etc.
  • a method according to the present invention may be adapted to measure the concentration of, for example, lactic acid, hydroxybutyric acid, etc.
  • Figure 2 illustrates an excitation signal suitable for use in a system and method according to the present invention in which some of the AC and DC components are applied simultaneously, indicated generally at 200, and having corresponding events numbered correspondingly to Figure 1 (so, for example, the signal 200 is initiated at time 201, and a strip is inserted at time 210, etc.).
  • the signal 200 has a frequency of about 10-20kHz and an amplitude of about 12.4-56.6m
  • a DC offset is superimposed, as shown at 270.
  • Typical AC and DC responses are shown in Figure 2. The AC and DC responses are measured simultaneously and mathematically deconvoluted and used to determine the impedance (admittance magnitude and phase) and the amperometric or coulometric response.
  • a system for measuring blood glucose advantageously employs a blood glucose meter and test strips generally similar to those used in prior art systems, such as those commercially available from Roche Diagnostics, and such as are described in U.S. Patents Nos. 6,270,637; and 5,989,917, which are hereby incorporated in their entireties.
  • These test strips provide apparati having a sample cell in which the blood sample is received for testing, and electrodes disposed within the sample cell through which the excitation signal is provided and the measurements are made.
  • these test strips and meters may advantageously be used for the measurement of glucose in blood, but that other apparati may be more suitable for the measurement of other analytes or other biological fluids when practising the present invention.
  • a suitable glucose meter may be adapted from such known meters by the addition of electronic circuitry that generates and measures signals having AC and DC components, such as those described hereinabove, and by being programmed to correct the DC measurement using the AC measurement(s), as described in greater detail hereinbelow.
  • AC and DC components such as those described hereinabove
  • the specific geometry and chemistry of the test strips can cause variations in the relationships between the concentration of glucose, hematocrit, and temperature, and the impedance of a sample.
  • a given combination of test strip geometry and chemistry must be calibrated, and the meter programmed with the corresponding algorithm.
  • the present invention comprehends the application of excitation signals in any order and combination. For example, the present invention comprehends the application of 1) AC only, 2) AC then DC, 3) AC then DC then AC, 4) DC then AC, and 5) AC with a DC offset, just to name a few of the possible permutations.
  • hematocrit value As an example, it is intended that such statements include not only determining the actual hematocrit value, but also a hematocrit correction factor vs. some nominal point. In other words, the process may never actually arrive at a number equal to the hematocrit value of the sample, but instead determine that the sample's hematocrit differs from a nominal value by a certain amount. Both concepts are intended to be covered by statements such as "determine the hematocrit value.”
  • Example 1 The measurements made in Example 1 were achieved using the test strip illustrated in Figures 3A-B and indicated generally at 300.
  • the test strip 300 includes a capillary fill space containing a relatively thick film reagent and working and counter electrodes, as described in U.S. Patent No. 5,997,817, which is hereby incorporated by reference.
  • the test strip 300 is commercially available from Roche Diagnostics Corporation (Indianapolis, DN) under the brand name Comfort Curve ®.
  • the ferricyanide reagent used had the composition described in Tables I and II.
  • a "dose response" study was performed, in which glycollyzed (glucose depleted) blood was divided into discrete aliquots and controlled levels of glucose were added to obtain five different known levels of glucose in the blood samples.
  • the resulting DC current profile was then examined as two parameters were varied.
  • the first parameter was the Incubation Time, or the time between the detection of the blood sample being applied to the test strip 300 and the application of the DC potential to the test strip 300.
  • the second parameter to be varied was the Read Time, or the time period after application of the DC potential and the measurement of the resulting current.
  • the length of time between detection of the blood sample being applied to the test strip to the taking of the last measurement used in the concentration determination calculations is the Total Test Time. In this study, therefore, the sum of the Incubation Time and the Read Time is the Total Test Time.
  • the results of this study are illustrated in Figures 5 and 6.
  • the barrier to implementation of such fast test times in a consumer glucose test device is the variation from blood sample to blood sample of the level of interference from the presence of blood cells in the sample.
  • the hematocrit (the percentage of the volume of a blood sample which is comprised of cells versus plasma) varies from individual to individual.
  • the interference effect of hematocrit on such measurements is fairly complex. In the tests of Example 1, however, all samples contained the same level of hematocrit. With no variable hematocrit influence at the different glucose levels, the hematocrit term cancels out in the correlation figures.
  • test strip 300 includes a capillary fill space containing a relatively thick film reagent and working and counter electrodes, as described in U.S. Patent No. 5,997,817, which is hereby inco ⁇ orated herein by reference.
  • capillary blood samples from various fingerstick donors were applied to test strip 300 and the excitation potentials illustrated in Figure 4 were applied to the electrodes.
  • the excitation comprised a 2 kHz 40 rnV rms AC signal applied between 0 seconds and approximately 4.5 seconds after sample application, followed by a 300 mV DC signal applied thereafter.
  • the AC response of the sample was derived as admittance (the inverse of impedance).
  • the admittance response is proportionate to the hematocrit level of the sample in a temperature dependent manner.
  • the relationship between admittance, hematocrit and testing temperature is illustrated in Figure 7.
  • the data used for the admittance charted in Figure 7 is the last admittance measurement made for each sample during the AC portion of the excitation illustrated in Figure 4. Regression analysis of this data allows admittance, hematocrit and temperature to be related according to the following formula:
  • Equation 1 c 0 , Ci and c 2 are constants, d ⁇ is the deviation in temperature from a center defined as “nominal” (24°C for example), and H eSt is the estimated deviation in hematocrit from a similar "nominal" value.
  • the actual hematocrit value is not necessary, and it is generally preferred to produce a response which is proportionate but centers around a nominal hematocrit.
  • the accuracy of the DC glucose response can be greatly improved by combining the estimated hematocrit, temperature and DC response to correct for the hematocrit interference in the DC response as follows:
  • Equation 2 where DC is the measured glucose current response to the applied DC signal and PRED is the compensated (predicted) glucose response corrected for the effects of hematocrit and temperature.
  • the constants (ao , hct] , hct 2 , tau 1; tau 2) a], hct 3? hct 4 , tau 3 and tau 4 ) in Equation 2 can be determined using regression analysis, as is known in the art.
  • Figure 8 illustrates the uncompensated 5.5 second DC glucose response of all of the capillary blood samples as temperature varies (ignoring the AC measurement data). As will be appreciated, there is a wide variation in the DC current response as temperature and hematocrit vary.
  • Figure 9 illustrates the correlation between the actual blood glucose level of the sample versus the predicted response using Equation 2. As can be seen, when the DC response is compensated for hematocrit levels using the AC response data, r 2 values of 0.9404 to 0.9605 are achieved with a Total Test Time of 5.5 seconds.
  • Example 3 Use of AC Phase Angle to Estimate Blood Glucose Levels and Hematocrit
  • Example 3 The measurements made in Example 3 were also achieved using the test strip illustrated in Figures 3A-B and indicated generally at 300.
  • the test strip 300 includes a capillary fill space containing a relatively thick film reagent and working and counter electrodes, as described in U.S. Patent No. 5,997,817, which is hereby inco ⁇ orated by reference. Because hematocrit levels from capillary blood samples typically vary only between 30% - 50%, spiked venous blood samples having a hematocrit range from 20% - 70% were used for this Example 3. Five levels of glucose, temperature (14, 21, 27, 36 and 42 °C) and hematocrit (20, 30, 45, 60 and 70%) were independently varied, producing a covariance study with 125 samples.
  • the excitation comprised a 2 kHz AC signal for approximately 4.1 seconds, a 1 kHz AC signal for approximately 0.1 seconds, and a 200 Hz signal for approximately 0.1 seconds. All three AC signals had an amplitude of 56.56 mV peak. No DC excitation was used in this example.
  • the Total Test Time was 4.3 seconds from sample application time.
  • phase angle is also a function of the sample glucose level in the case of this test strip and reagent.
  • Figure 11 where the AC phase angle for each of the three test frequencies is plotted versus the reference glucose level. Regression analysis for each of the three frequencies produces AC phase angle-to-reference glucose level r 2 correlation values of 0.9114 at 2 kHz, 0.9354 at 1 kHz, and 0.9635 at 200 Hz.
  • the present invention therefore comprehends the use of the AC phase angle to measure glucose levels.
  • the AC excitation frequency producing the measured phase angle is preferably 2 kHz or below, more preferably 1 kHz or below, and most preferably 200 Hz or below, but not including DC excitation.
  • the linearized relationship between the 200 Hz phase angle response and the blood glucose level is as follows:
  • the resulting compensated (predicted) response PRED versus glucose for the 125 blood samples is shown in Figure 12.
  • This Example 3 demonstrates again the value of AC measurements for compensating for interferants that reduce the accuracy of blood glucose measurements. Using an existing commercially available sensor, the present invention yields a 4.3 second Total Test Time with an overall r 2 of 0.9870.
  • Glu is the known glucose concentration
  • HCT is the known hematocrit concentration
  • Temp is the known temperature.
  • the determined coefficients revealed that the temperature coefficient (c 3 ) was essentially zero at 20 kHz and 10 kHz, cancelling temperature from the equation at these frequencies.
  • the glucose coefficient (c is essentially zero at all of the AC frequencies because, as explained hereinabove, the higher frequency AC impedance measurements are largely unaffected by glucose levels and are therefore useful for measuring the levels of interfering substances. It was therefore found that the hematocrit level could be determined independent of temperature and glucose level using only the AC phase angle measurements. In a preferred embodiment, the hematocrit may be measured using the phase angle data from all four measured frequencies:
  • the coefficients can be empirically determined for any particular test strip architecture and reagent chemistry.
  • the present invention therefore may be used to estimate hematocrit using only AC phase angle measurements preferably made at at least one AC frequency, more preferably made at at least two AC frequencies, and most preferably made at at least four AC frequencies.
  • Example 4 The measurements made in Example 4 were also achieved using the test strip illustrated in Figures 3A-B and indicated generally at 300.
  • the test strip 300 includes a capillary fill space containing a relatively thick film reagent and working and counter electrodes, as described in U.S. Patent No. 5,997,817, which is hereby inco ⁇ orated by reference.
  • the test strip was modified from that described in U.S. Patent No. 5,997,817, however, by the use of a different reagent.
  • the nitrosoaniline reagent used had the composition described in Tables III and IV.
  • nitrosoaniline reagent is as follows:
  • Step 1 Prepare a buffer solution by adding 1.54g of dibasic potassium phosphate (anhydrous) to 43.5 g of deionized water. Mix until the potassium phosphate is dissolved.
  • Step 2 To the solution from step 1, add 1.14g of monobasic potassium phosphate and mix until dissolved.
  • Step 3 To the solution from step 2, add 0.59g of disodium succinate (hexahydrate) and mix until dissolved.
  • Step 4 Verify that the pH of the solution from step 3 is 6.7 +/- 0.1. Adjustment should not be necessary.
  • Step 5 Prepare a 5g aliquot of the solution from step 4, and to this add 113 kilounits (by DCIP assay) of the apoenzyme of quinoprotein glucose dehydrogenase (EC#: 1.1.99.17). This is approximately 0.1646g. Mix, slowly, until the protein is dissolved.
  • Step 6 To the solution from step 5, add 4.2 milligrams of PQQ and mix for no less than 2 hours to allow the PQQ and the apoenzyme to reassociate in order to provide functional enzyme.
  • Step 7 To the solution from step 4, add 0.66g of the mediator precursor, N,N- bis(hydroxyethyl)-3-methoxy-4-nitrosoaniline (hydrochloride) (BM 31.1144). Mix until dissolved (this solution will have a greenish black coloration).
  • Step 8 Measure the pH of the solution from step 7 and adjust the pH to a target of 7.0 +/- 0.1. Normally this is accomplished with 1.197g of 5N potassium hydroxide. Because the specific amount of potassium hydroxide may vary as needed to reach the desired pH, generally deviations in mass from the 1.197g are made up from an aliquot of 3.309g deionized water which is also added at this step.
  • Step 9 Prepare a solution of Natrosol 250M (available from Aqualon), by slowly sprinkling 0.047g over 44.57g of deionized water which is mixed (using a rotary mixer and blade impeller) at a rate of approximately 600 ⁇ m in a vessel of sufficient depth such that the rotor blades are not exposed nor the solution running over. Mix until the Natrosol is completely dissolved.
  • Step 10 Prepare a suspension of Avicel RC-591F (available from FMS), by slowly sprinkling 0.54g onto the surface of the solution from step 9, mixing at a rate of approximately 600 ⁇ m for not less than 60 minutes before proceeding.
  • Step 11 To the suspension from step 10, gradually add 0.8 lg of Polyethylene oxide of 300kDa mean molecular weight while mixing and continue to mix for not less than 60 minutes before proceeding.
  • Step 12 Gradually add the solution from step 8 to the suspension from step 11 while mixing. Reduce the mixing rate to 400 ⁇ m.
  • Step 13 To the reagent from step 12, add 1.89g of Trehalose and continue mixing for not less than 15 minutes.
  • Step 14 To the reagent from step 13, add 32.7mg of Triton X-100 (available from Roche Diagnostics) and continue mixing.
  • Triton X-100 available from Roche Diagnostics
  • Step 15 To the reagent from step 14, add the enzyme solution from step 6. Mix for no less than 30 minutes. At this point the reagent is complete. At room teperature the wet reagent mass is considered acceptable for use for 24 hours.
  • Spiked venous blood samples were used. Five levels of glucose, four temperatures (19, 23, 32 and 38 °C) and five levels of hematocrit (20, 30, 45, 60 and 70%) were independently varied, producing a covariance study with 100 samples. 16 test strips 300 were tested for each unique combination of glucose, temperature and hematocrit. The blood samples were applied to test strip 300 and the excitation potentials illustrated in Figure 13 were applied to the electrodes.
  • the excitation comprised a 3.2 kHz AC signal for approximately 4.0 seconds, a 2.13 kHz AC signal for approximately 0.1 seconds, a 1.07 kHz AC signal for approximately 0.1 seconds, a 200 Hz AC signal for approximately 0.1 seconds, a 25 Hz AC signal for approximately 0.1 seconds, followed by a DC signal of 550 mV for approximately 1.0 second. All four AC signals had an amplitude of 56.56 mV peak.
  • the Total Test Time was 5.5 seconds from sample application time.
  • the AC response of the sample was derived as admittance (the inverse of impedance).
  • the admittance response is proportionate to the hematocrit level of the sample in a temperature dependent manner.
  • the relationship between admittance, hematocrit and testing temperature is illustrated in Figure 14.
  • T x HCT cross product term
  • Equation 7 Co, Ci, c 2 and c 3 are constants, dT is the deviation in temperature from a center defined as “nominal” (24°C for example), and H eSt is the estimated deviation in hematocrit from a similar "nominal" value.
  • the actual hematocrit value is not necessary, and it is generally preferred to produce a response which is proportionate but centers around a nominal hematocrit.
  • Equation 8 The constants in Equation 8 can be determined using regression analysis, as is known in the art.
  • Figure 15 illustrates the uncompensated 5.5 second DC glucose response of all of the blood samples as hematocrit and temperature vary (ignoring the AC measurement data). As will be appreciated, there is a wide variation in the DC current response as temperature and hematocrit vary.
  • Figure 16 illustrates the correlation between the actual blood glucose level of the sample versus the predicted response using Equation 8. As can be seen, when the DC response is compensated for hematocrit levels using the AC response data, an overall r 2 value of 0.9818 is achieved with a Total Test Time of 5.5 seconds. This demonstrates the applicability of the present invention in achieving high accuracy and fast test times with a different reagent class than was used in Examples 1-3.
  • Example 5 Combined AC and DC Measurement Using a 0.397 ⁇ l Sample
  • test strip 1700 comprises a bottom foil layer 1702 formed from an opaque piece of 350 ⁇ m thick polyester (in the preferred embodiment this is Melinex 329 available from DuPont) coated with a 50 nm conductive (gold) layer (by sputtering or vapor deposition, for example). Electrodes and connecting traces are then patterned in the conductive layer by a laser ablation process to form working, counter, and dose sufficiency electrodes (described in greater detail hereinbelow) as shown.
  • Melinex 329 available from DuPont
  • the laser ablation process is performed by means of an excimer laser which passes through a chrome-on-quartz mask.
  • the mask pattern causes parts of the laser field to be reflected while allowing other parts of the field to pass through, creating a pattern on the gold which is ejected from the surface where contacted by the laser light.
  • the bottom foil layer 1702 is then coated in the area extending over the electrodes with a reagent layer 1704 in the form of an extremely thin reagent film.
  • This procedure places a stripe of approximately 7.2 millimeters width across the bottom foil 1702 in the region labelled "Reagent Layer" on Figure 17. In the present Example, this region is coated at a wet-coat weight of 50 grams per square meter of coated surface area leaving a dried reagent less than 20 ⁇ m thick.
  • the reagent stripe is dried conventionally with an in-line drying system where the nominal air temperature is at 110°C. The rate of processing is nominally 30-38 meters per minute and depends upon the rheology of the reagent.
  • the materials are processed in continuous reels such that the electrode pattern is orthogonal to the length of the reel, in the case of the bottom foil 1702.
  • the spacer is slit and placed in a reel-to-reel process onto the bottom foil 1702.
  • Two spacers 1706 formed from 100 ⁇ m polyester (in the preferred embodiment this is Melinex 329 available from DuPont) coated with 25 ⁇ m PSA (hydrophobic adhesive) on both the dorsal and ventral surfaces are applied to the bottom foil layer 1702, such that the spacers 1706 are separated by 1.5 mm and the working, counter and dose sufficiency electrodes are centered in this gap.
  • the hydrophilic film is coated with a mixture of Vitel and Rhodapex surfactant at a nominal thickness of 10 microns.
  • the top foil layer 1708 is laminated using a reel-to-reel process. The sensors can then be produced from the resulting reels of material by means of slitting and cutting.
  • the 1.5 mm gap in the spacers 1706 therefore forms a capillary fill space between the bottom foil layer 1702 and the top foil layer 1708.
  • the hydrophobic adhesive on the spacers 1706 prevents the test sample from flowing into the reagent under the spacers 1706, thereby defining the test chamber volume. Because the test strip 1700 is 5 mm wide and the combined height of the spacer 1706 and conductive layer is 0.15 mm, the sample receiving chamber volume is
  • the volume of sample needed to sufficiently cover the working, counter and dose sufficiency electrodes i.e. the minimum sample volume necessary for a measurement.
  • the reagent composition for the test strip 1700 is given in Tables V and VI.
  • Mass per Sensor is the amount of the component within the capillary; this does not reflect the reagent that is outside of the capillary.
  • Step 1 Prepare a buffer solution by adding 1.654g of dibasic potassium phosphate (trihydrous) to 31.394 g of deionized water. Mix until the potassium phosphate is dissolved.
  • Step 2 To the solution from step 1, add 0.941g of monobasic potassium phosphate and mix until dissolved.
  • Step 3 To the solution from step 2, add 0.285g of disodium succinate (hexahydrate) and mix until dissolved.
  • Step 4 Verify that the pH of the solution from step 3 is 6.8 +/- 0.1. Adjustment should not be necessary.
  • Step 5 Prepare a 4.68g aliquot of the solution from step 4, and to this add 229 kilounits (by DCIP assay) of the apoenzyme of quinoprotein glucose dehydrogenase (EC#: 1.1.99.17). This is approximately 0.3321g. Mix, slowly, until the protein is dissolved.
  • Step 6 To the solution from step 5, add 9.3 milligrams of PQQ and mix for no less than 2 hours to allow the PQQ and the apoenzyme to reassociate in order to provide functional enzyme.
  • Step 7 Prepare a solution by dissolving 0.772g of Trehalose into 1.218g of deionized water.
  • Step 8 After enzyme reassociation, add the solution from step 7 to the solution from step 6 and continue mixing for not less than 30 minutes.
  • Step 9 To the solution from step 4, add 0.690g of the mediator precursor BM 31.1144. Mix until dissolved (this solution will have a greenish black coloration).
  • Step 10 Measure the pH of the solution from step 9 and adjust the pH to a target of 7.0 +/- 0.1. Normally this is accomplished with 1.006g of 5N potassium hydroxide. Because the specific amount of potassium hydroxide may vary as needed to reach the desired pH, generally deviations in mass from the 1.006g are made up from an aliquot of 3.767g deionized water which is also added at this step.
  • Step 11 Prepare a solution of Natrosol 250M (available from Aqualon), by slowly sprinkling 0.350g over 56.191g of deionized water which is mixed (using a rotary mixer and blade impeller) at an initial rate of approximately 600 ⁇ m in a vessel of sufficient depth such that the rotor blades are not exposed nor the solution running over. As the Natrosol dissolves, the mixing rate needs to be increased to a speed of 1.2 - 1.4 k ⁇ m. Mix until the Natrosol is completely dissolved. Note that the resulting matrix will be extremely viscous - this is expected.
  • Natrosol 250M available from Aqualon
  • Step 12 To the solution from step 11, gradually add 0.350g of Sodium- Carboxymethylcellulose 7HF (available from Aqualon). Mix until the polymer is dissolved.
  • Sodium- Carboxymethylcellulose 7HF available from Aqualon
  • Step 13 To the suspension from step 13, gradually add 1.0 lg of Polyethylene oxide of 300kDa mean molecular weight while mixing and continue to mix for not less than 60 minutes before proceeding.
  • Step 14 Gradually add the solution from step 10 to the suspension from step 13 while mixing.
  • Step 15 To the reagent from step 14, add 34.2mg of Triton X-100 (available from Roche Diagnostics) and continue mixing.
  • Triton X-100 available from Roche Diagnostics
  • Step 16 To the reagent from step 15, add the enzyme solution from step 8. Mix for no less than 30 minutes. At this point the reagent is complete. At room teperature the wet reagent mass is considered acceptable for use for 24 hours.
  • the measurement results illustrated in FIG. 18 show the correlation coefficient r 2 between the DC current response and the glucose level as the Read Time varies for three combinations of temperature and hematocrit. These results demonstrate that a robust DC response should be anticipated for tests as fast as 1 second. However, those skilled in the art will recognise that there are undesirable variations in the sensor accuracy (correlation) due to the interfering effects of temperature and hematocrit levels, suggesting that the combined AC and DC measurement method of the present invention should produce more closely correlated results. Based upon the encouraging results obtained in Figure 18, a further test was designed using the excitation signal of Figure 19 applied to the test strip 1700.
  • the excitation comprised a 10 kHz AC signal applied for approximately 1.8 seconds, a 20 kHz AC signal applied for approximately 0.2 seconds, a 2 Hz AC signal applied for approximately 0.2 seconds, a 1Hz AC signal applied for approximately 0.2 seconds, and a DC signal applied for approximately 0.5 seconds.
  • the AC signals had an amplitude of 12.7 mV peak, while the DC signal had an amplitude of 550 mV.
  • the Total Test Time was 3.0 seconds.
  • phase angle of the 20 kHz AC response is plotted versus hematocrit in Figure 21.
  • the results for phase angle measured at 10 kHz are similar.
  • the hematocrit of the blood sample may therefore be reliably estimated using only the phase angle information as follows:
  • the correlation between phase angle and hematocrit was better at higher frequencies. Because of this, the c 2 constant approaches zero and Hest can reliably be estimated using only the 10 kHz and 20 kHz data. Use of lower frequencies, however, allows for slight improvements in the strip-to-strip variability of the H eSt function.
  • the present invention therefore may be used to estimate hematocrit using only AC phase angle measurements preferably made at at least one AC frequency, more preferably made at at least two AC frequencies, and most preferably made at at least four AC frequencies.
  • a thermistor is placed in the test meter near where the test strip is inserted into the meter. Because the thermistor is measuring a temperature remote from the actual sample, it is at best only a rough approximation of the true sample temperature. Furthermore, if the sample temperature is changing (for example due to evaporation), then the thermal inertia of the test meter and even the thermistor itself will prevent the meter-mounted thermistor from accurately reflecting the true temperature of the sample under test.
  • the temperature estimation of the present invention is derived from measurements made within the sample under test (i.e. within the reaction zone in which the sample under test reacts with the reagent), thereby eliminating any error introduced by the sample being remote from the measuring location. Additionally, the temperature estimation of the present invention is made using data that was collected very close in time to the glucose measurement data that will be corrected using the temperature estimation, thereby further improving accuracy. This represents a significant improvement over the prior art methods.
  • Equation 13 The constants in Equation 13 can be determined using regression analysis, as is known in the art.
  • the present invention therefore allows one to estimate hematocrit by using the AC phase angle response (Equation 11).
  • the estimated hematocrit and the measured AC admittance can be used to determine the estimated temperature (Equation 12).
  • the estimated hematocrit and estimated temperature can be used with the measured DC response to obtain the predicted glucose concentration (Equation 13).
  • the excitation profile illustrated in Figure 24 was utilized in order to decrease the Total Test Time. As described above with respect to Example 5, it was determined that the phase angle at 20 kHz and at 10 kHz were most closely correlated with the hematocrit estimation. It was therefore decided to limit the AC portion of the excitation to these two frequencies in Example 6 in order to decrease the Total Test Time. In order to make further reductions in Total Test Time, the 10 kHz AC excitation was applied simultaneously with the DC signal (i.e. an AC signal with a DC offset), the theory being that this combined mode would allow for the collection of simultaneous results for DC current, AC phase and AC admittance, providing the fastest possible results. Therefore, the 20 kHz signal was applied for 0.9 seconds. Thereafter, the 10 kHz and DC signals were applied simultaneously for 1.0 second after a 0.1 second interval.
  • the DC signal i.e. an AC signal with a DC offset
  • Example 6 49 spiked venous blood samples representing seven glucose levels and seven hematocrit levels were tested.
  • the correlation coefficient r between the DC current and the blood hematocrit was then examined at three DC measurement times: 1.1 seconds, 1.5 seconds and 1.9 seconds after sample application. These correlations are plotted versus hematocrit level in Figure 25. All of these results are comparable, although the correlation is generally poorest at 1.1 seconds and generally best at 1.5 seconds. The minimum correlation coefficient, however, exceeds 0.99.
  • Figure 26 illustrates the phase angle at 20 kHz plotted against hematocrit levels.
  • the correlation between these two sets of data is very good, therefore it was decided that the 10 kHz data was unnecessary for estimating hematocrit.
  • the hematocrit can therefore be estimated solely from the 20 kHz phase angle data as follows:
  • Figure 27 illustrates the DC current response versus glucose level for all measured hematocrit levels as the read time is varied between 1.1 seconds, 1.5 seconds and 1.9 seconds. Not su ⁇ risingly, the DC current at 1.1 seconds is greater than the DC current at 1.5 seconds, which is greater than the DC current at 1.9 seconds. Those skilled in the art will recognise that the hematocrit level has a large effect on the DC current, particularly at high glucose concentrations.
  • the accuracy of the DC glucose response can be greatly improved by compensating for the interference caused by hematocrit as follows:
  • Equation 15 does not include temperature compensation terms since temperature variation was not included in the experiment of this Example 6, it can be reasonably inferred from previous examples that a Test term could be included using the 10 kHz and 20 kHz admittance values in combination with the H eSt term. Because the hematocrit can be reliably estimated using only the 20 kHz phase angle measurement data, the hematocrit compensated predicted glucose response can be determined using only this phase angle information and the measured DC response. The compensated DC response versus glucose level for only the DC read at 1.1 seconds (representing a 1.1 second Total Test Time) is illustrated in Figure 28. The data shows an overall r 2 correlation of 0.9947 with a 1.1 second Total Test Time.
  • Example 7 Use of AC Phase Angle to Detect an Abused Sensor
  • Cottrell Failsafe Ratio CFR
  • the Cottrell response of the biosensor in the Confidence system can be given by:
  • n electrons freed per glucose molecule
  • NCFR Cottrell failsafe ratio
  • a Current Sum Failsafe can be devised that places a check on the Cottrell response of the sensor by summing all of the acquired currents during sensor measurement. When the final current is acquired, it is multiplied by two constants (which may be loaded into the meter at the time of manufacture or, more preferably, supplied to the meter with each lot of sensors, such as by a separate code key or by information coded onto the sensor itself). These constants represent the upper and lower threshold for allowable NCFR values.
  • the two products of the constants multiplied by the final current are compared to the sum of the biosensor currents.
  • the sum of the currents should fall between the two products, thereby indicating that the ratio above was fulfilled, plus or minus a tolerance. Therefore, the preferred embodiment performs the following check when there is a single DC block: m
  • MCFR Modified Cottrell Failsafe Ratio
  • NCFRj the Normalized Cottrell Failsafe Ratios
  • the preferred embodiment performs the following check when there are two DC blocks:
  • the NCFR (and MCFR) is correlated with hematocrit.
  • the AC phase angle is also correlated with hematocrit. It follows then, that the AC phase angle and the NCFR are correlated with one another. This relationship holds only if the sensor is unabused. The correlation degrades for an abused sensor.
  • FAILSAFE 1000 x arctan[NCFR/(fs 0 + fs ⁇ ( ⁇ 10 kHz - 2 0 kHz))] (Equation
  • Equation 21 the intercept term fs 0 can be chosen such that a
  • each of these solutions each inco ⁇ orate one or the other electrode of the measurement pair in communication with either the upstream or the downstream indicator electrodes to assess the presence of a sufficient volume of sample to avoid biased test results.
  • failure modes persist wherein the devices remain prone to misinte ⁇ retation of sample sufficiency.
  • the present inventors have determined that such erroneous conclusions are related primarily to the distances between a downstream member of a measurement electrode pair (co- planar or opposing geometries) and the dose detection electrode, in combination with the diversity of non-uniform flow fronts.
  • a sample traversing the capillary fill space having an aberrant (uneven) flow front can close the circuit between a measurement electrode and an indicator electrode and erroneously advise the system that sufficient sample is present to avoid a biased measurement result.
  • Another problem with prior art dose sufficiency methodologies determined by the present inventors relates to the use of one or the other of the available measurement electrodes in electrical communication with an upstream or downstream dose detection electrode.
  • the stoichiometry of the measurement zone (the area above or between the measurement electrodes) is perturbed during the dose detect/dose sufficiency test cycle prior to making a measurement of the analyte of interest residing in the measurement zone.
  • sample matrices vary radically in make-up, the fill properties of these samples also vary, resulting in timing differences between sample types.
  • Such erratic timing routines act as an additional source of imprecision and expanded total system error metrics.
  • Example 8 Determination of Fluid Flow Front Behavior in a Capillary Fill Space
  • test fixtures comprising two sheets of clear polycarbonate sheets joined together with double-sided adhesive tape were used, where the capillary fill space was formed by cutting a channel in the double- sided tape.
  • Use of the polycarbonate upper and lower sheets allowed the flow fronts of the sample to be videotaped as it flowed through the capillary fill space.
  • the test devices were laminated using laser cut 1mm thick Lexan® polycarbonate sheets (obtained from Cadillac Plastics Ltd., Westlea, Swindon SN5 7EX, United Kingdom). The top and bottom polycarbonate sheets were coupled together using double-sided adhesive tapes (#200MP High
  • the capillary channels were defined by laser cutting the required width openings into the double-sided tape. Tape thicknesses of 0.05 ⁇ m, 0.125 ⁇ m, and 0.225 ⁇ m were used to give the required channel heights. The dimensions of the capillary spaces of the test devices are tabulated in FIG. 31.
  • top and bottom polycarbonate parts were laminated together with the laser cut adhesive tapes using a custom-built jig to ensure reproducible fabrication.
  • a fluid receptor region defineing the entrance to the capillary channel was formed by an opening pre-cut into the upper polycarbonate sheet and adhesive tape components.
  • channel widths 0.5mm, 1.00mm, 1.5mm, 2.00mm, 3.00mm, and 4.00mm were fabricated.
  • the capillary channel length for all devices was 50mm. Twenty-eight (28) of each of the eighteen (18) device types were constructed.
  • the assembled devices were plasma treated by Weidman Plastics Technology of Dortmund, Germany. The following plasma treatment conditions were used:
  • Microwave plasma processor 400 Microwave plasma processor 400
  • the plasma-treated devices were stored at 2 - 8°C when not in use. The devices were allowed to equilibrate to room temperature for one (1) hour minimum before use.
  • Each of the test devices was dosed with a fixed volume of venous blood having a hematocrit value of 45%.
  • Flow and flow front behavior was captured on videotape for later analysis. It was determined that the relative dimensions of the capillary fill channel determined the flow front behavior.
  • Devices to the left of the dashed line in FIG. 31 (devices A2, A4, B2, B4, B5, C2, C4, and C5) resulted in a convex flow front behavior, while devices to the right of the dashed line (devices A6, A8, Al l, B6, B8, Bll, C6, C8, and Cll) displayed a concave flow front behavior.
  • Both the convex and concave flow front behaviors are schematically illustrated in FIG. 31. This data shows that the aspect ratio between the height and the width of the capillary fill space is a determining factor in whether the sample flow front is convex or concave.
  • FIGs. 32A-C The problems associated with a concave flow front in a capillary fill space are illustrated in FIGs. 32A-C.
  • the test strip includes a working electrode 3200, a reference electrode 3202, and a downstream dose sufficiency electrode 3204 that works in conjunction with one of the measurement electrodes 3200 or 3202.
  • FIGs. 32A-C illustrate that a sample flow front exhibiting a concave shape can also cause biased measurement results. In each drawing, the direction of sample travel is shown by the arrow. In FIG.
  • the portions of the sample adjacent to the capillary walls have reached the dose sufficiency electrode 3204, thereby electrically completing the DC circuit between this electrode and one of the measurement electrode pair that is being monitored by the test meter in order to make the dose sufficiency determination.
  • the test meter will conclude that there is sufficient sample to make a measurement at this time, the sample clearly has barely reached the reference electrode 3202 and any measurement results obtained at this time will be highly biased.
  • FIG. 32B illustrates the situation where the dose sufficiency electrode 3204 has been contacted (indicating that the measurement should be started), but the reference electrode 3202 is only partially covered by the sample. Although the sample has reached the reference electrode 3202 at this time, the reference electrode 3202 is not completely covered by sample, therefore any measurement results obtained at this time will be partially biased. Both of the situations illustrated in FIGs. 32A-B will therefore indicate a false positive for dose sufficiency, thereby biasing the measurement test results. Only in the situation illustrated in FIG. 32C, where the reference electrode 3202 is completely covered by the sample, will the measurement results be unbiased due to the extent of capillary fill in the measurement zone.
  • the present invention solves the stoichiometric problems associated with the prior art designs pairing the dose sufficiency electrode with one of the measurement electrodes when making the dose sufficiency determination.
  • the present invention comprehends a test strip having an independent pair of dose sufficiency electrodes positioned downstream from the measurement electrodes.
  • the test strip is indicated generally as 3300, and includes a measurement electrode pair consisting of a counter electrode 3302 and a working electrode 3304.
  • the electrodes may be formed upon any suitable substrate in a multilayer test strip configuration as is known in the art and described hereinabove.
  • the multilayer configuration of the test strip provides for the formation of a capillary fill space 3306, also as known in the art.
  • a dose sufficiency working electrode 3308 and a dose sufficiency counter electrode 3310 are formed within the capillary fill space 3306, and downstream (relative to the direction of sample flow) from the measurement electrodes 3302 and 3304.
  • the test meter When the test strip 3300 is inserted into the test meter, the test meter will continuously check for a conduction path between the dose sufficiency electrodes 3308 and 3310 in order to determine when the sample has migrated to this region of the capillary fill space. Once the sample has reached this level, the test meter may be programmed to conclude that the measurement electrodes are covered with sample and the sample measurement sequence may be begun. It will be appreciated that, unlike as required with prior art designs, no voltage or current need be applied to either of the measurement electrodes 3302 and 3304 during the dose sufficiency test using the test strip design of FIG. 33.
  • the test strip 3300 is also desirable for judging dose sufficiency when the capillary fill space is designed to produce samples that exhibit a convex flow front while filling the capillary fill space 3306, as illustrated in FIG. 34A. As can be seen, the measurement zone above the measurement electrodes 3302 and 3304 is covered with sample when the convex flow front reaches the dose sufficiency electrode pair 3308,3310.
  • the test strip design 3300 may not, however, produce ideal results if the capillary fill space 3306 allows the sample to exhibit a concave flow front while filling, as shown in FIG. 34B.
  • the peripheral edges of the concave flow front reach the dose sufficiency electrodes 3308,3310 before the measurement zone has been completely covered with sample.
  • the dose sufficiency electrodes 3308,3310 will indicate sample sufficiency as soon as they are both touched by the edges of the flow front. Therefore, the dose sufficiency electrode design shown in the test strip of FIG. 33 works best when the sample filling the capillary space 3306 exhibits a convex flow front.
  • the dose sufficiency electrodes 3308,3310 have their longest axis within the capillary fill space 3306 oriented pe ⁇ endicular to the longitudinal axis of the capillary fill space 3306. Such electrodes are referred to herein as "pe ⁇ endicular dose sufficiency electrodes.”
  • An alternative dose sufficiency electrode arrangement is illustrated in FIGs. 35A-B. As shown in FIG. 35A, the present invention also comprehends a test strip having an independent pair of dose sufficiency electrodes positioned downstream from the measurement electrodes, where the dose sufficiency electrodes have their longest axis within the capillary fill space oriented parallel to the longitudinal axis of the capillary fill space.
  • the test strip in FIG. 35 is indicated generally as 3500, and includes a measurement electrode pair consisting of a counter electrode 3502 and a working electrode 3504.
  • the electrodes may be formed upon any suitable substrate in a multilayer test strip configuration as is known in the art and described hereinabove.
  • the multilayer configuration of the test strip provides for the formation of a capillary fill space 3506, also as known in the art.
  • a dose sufficiency working electrode 3508 and a dose sufficiency counter electrode 3510 together forming a parallel dose sufficiency electrode pair.
  • test meter When the test strip 3500 is inserted into the test meter, the test meter will continuously check for a conduction path between the dose sufficiency electrodes 3508 and 3510 in order to determine when the sample has migrated to this region of the capillary fill space. Once the sample has reached this level, the test meter may be programmed to conclude that the measurement electrodes are covered with sample and the sample measurement sequence may be begun. It will be appreciated that, as with the test strip 3300 (and unlike as required with prior art designs), no voltage or current need be applied to either of the measurement electrodes 3502 and 3504 during the dose sufficiency test using the test strip design of FIG. 35.
  • the stoichiometry of the measurement zone is not perturbed during the dose sufficiency test cycle prior to making a measurement of the analyte of interest residing in the measurement zone. This represents a significant improvement over the dose sufficiency test methodologies of the prior art.
  • a further improved operation is realized with the parallel dose sufficiency electrodes of the test strip 3500 when the dose sufficiency electrodes are energized with a relatively high frequency AC excitation signal.
  • the dose sufficiency electrodes 3508,3510 display significant edge effects, wherein the excitation signal traverses the gap between the electrodes only when the electrode edges along the gap are covered with the sample fluid.
  • the test strip 3500 is illustrated in enlarged size in FIG. 36 (with only the electrode portions lying within the capillary fill space 3506 and the strip-to-meter electrode contact pads visible).
  • the gap width GW between the edges of the dose sufficiency electrodes 3508,3510 is preferably 100-300 ⁇ m, more preferably 150- 260 ⁇ m, and most preferably 255 ⁇ m.
  • a smaller gap width GW increases the amount of signal transmitted between dose sufficiency electrodes whose edges are at least partially covered by sample; however, the capacitance of the signal transmission path increases with decreasing gap width GW.
  • An advantage of the parallel dose sufficiency electrode design of FIGs. 35 and 36, when used with AC excitation, is that there is substantially no electrical communication between the electrodes until the sample covers at least a portion of the edges along the electrode gap. Therefore, a sample exhibiting the concave flow front of FIG. 35A, where the illustrated sample is touching both of the dose sufficiency electrodes 3508,3510 but is not touching the electrode edges along the gap, will not produce any significant electrical communication between the dose sufficiency electrodes. The test meter will therefore not form a conclusion of dose sufficiency until the sample has actually bridged the dose sufficiency electrodes between the electrode edges along the gap.
  • a conclusion of dose sufficiency can therefore be withheld until the sample has covered a predetermined portion of the dose sufficiency electrode gap edge.
  • an analysis of the dose sufficiency signal will allow the test meter to record the percentage of fill of the capillary fill space for each measurement made by the test meter, if desired. While the electrode geometry itself demonstrates an advantage over previous embodiments in terms of detecting an adequate sample, particularly in the case of a convex flow front, it was found that further improvement is achieved in the use of AC responses over DC responses for sample detection. DC responses have the problems of being sensitive to variations in, for example, temperature, hematocrit and the analyte (glucose for example).
  • AC responses at sufficiently high frequency can be made robust to the variation in the analyte concentration.
  • the AC response generated at sufficiently high frequencies in such capillary fill devices is primarily limited by the amount of the parallel gap between the electrode edges which is filled by the sample.
  • little or no AC response in this case admittance
  • the sensor can be made more or less sensitive as is deemed advantageous, with a higher threshold for admittance requiring more of the parallel gap to be filled before test initiation.
  • a further limitation of existing devices is the inability of the electrode geometry to discern the amount of time needed to fill the capillary space of the sensor.
  • a signal is first applied across the measurement electrodes prior to dosing. When a response is observed, the potential is immediately switched off and a second signal is applied across the dose sufficiency electrodes during which time the system both looks for a response to the signal (indicating electrode coverage) and marks the duration between the first event (when a response is observed at the measurement electrodes) and the second event (when a response is observed at the dose sufficiency electrodes).
  • the preferred embodiment uses an AC signal at sufficiently high frequency to avoid unnecessarily perturbing the electrochemical response at the measurement electrodes and to provide robust detection with respect to flow front irregularities.

Abstract

A method of measuring an analyte in a biological fluid using a test strip which comprises a capillary test chamber extending a length along the test strip, and two sets of electrodes in operative communication with the chamber, the method comprising the steps of dosing the test strip with a biological fluid, applying in consecutive order test signals to the two sets of electrodes and measuring the respective response signals, and performing a measurement upon the biological fluid. The said response signals may be used for determining a fill time value which could be compared to a predetermined value.

Description

METHOD FOR ANALYTE MEASUREMENT EMPLOYING MAXIMUM DOSING TIME DELAY
CROSS-REFERENCE TO RELATED APPLICATIONS
5
This application claims the benefit of U.S. Provisional Application No. 60/480,298, filed June 20, 2003. The contents of this application are hereby incorporated by reference herein.
10 TECHNICAL FIELD OF THE INVENTION
The present invention relates to a measurement method and apparatus for use in measuring concentrations of an analyte in a fluid. The invention relates more particularly, but not exclusively, to a method and apparatus which may be 15 used for measuring the concentration of glucose in blood.
BACKGROUND OF THE INVENTION
Measuring the concentration of substances, particularly in the presence of 20 other, confounding substances, is important in many fields, and especially in medical diagnosis. For example, the measurement of glucose in body fluids, such as blood, is crucial to the effective treatment of diabetes.
Diabetic therapy typically involves two types of insulin treatment: basal, and meal-time. Basal insulin refers to continuous, e.g. time-released insulin, often 25 taken before bed. Meal-time insulin treatment provides additional doses of faster acting insulin to regulate fluctuations in blood glucose caused by a variety of factors, including the metabolization of sugars and carbohydrates. Proper regulation of blood glucose fluctuations requires accurate measurement of the concentration of glucose in the blood. Failure to do so can produce extreme 30 complications, including blindness and loss of circulation in the extremities, which can ultimately deprive the diabetic of use of his or her fingers, hands, feet, etc. Multiple methods are known for measuring the concentration of analytes in a blood sample, such as, for example, glucose. Such methods typically fall into one of two categories: optical methods and electrochemical methods. Optical methods generally involve reflectance or absorbance spectroscopy to observe the spectrum shift in a reagent. Such shifts are caused by a chemical reaction that produces a color change indicative of the concentration of the analyte. Electrochemical methods generally involve, alternatively, amperometric or coulometric responses indicative of the concentration of the analyte. See, for example, U.S. Patent Nos. 4,233,029 to Columbus, 4,225,410 to Pace, 4,323,536 to Columbus, 4,008,448 to Muggli, 4,654,197 to Lilja et al., 5,108,564 to Szuminsky et al., 5,120,420 to Nankai et al., 5,128,015 to Szuminsky et al., 5,243,516 to White, 5,437,999 to Diebold et al., 5,288,636 to Pollmann et al., 5,628,890 to Carter et al., 5,682,884 to Hill et al., 5,727,548 to Hill et al., 5,997,817 to Crismore et al., 6,004,441 to Fujiwara et al., 4,919,770 to Priedel, et al., and 6,054,039 to Shieh, which are hereby incorporated in their entireties.
An important limitation of electrochemical methods of measuring the concentration of a chemical in blood is the effect of confounding variables on the diffusion of analyte and the various active ingredients of the reagent. For example, the geometry and state of the blood sample must correspond closely to that upon which the signal-to-concentration mapping function is based.
The geometry of the blood sample is typically controlled by a sample- receiving portion of the testing apparatus. In the case of blood glucose meters, for example, the blood sample is typically placed onto a disposable test strip that plugs into the meter. The test strip may have a sample chamber (capillary fill space) to define the geometry of the sample. Alternatively, the effects of sample geometry may be limited by assuring an effectively infinite sample size. For example, the electrodes used for measuring the analyte may be spaced closely enough so that a drop of blood on the test strip extends substantially beyond the electrodes in all directions. Ensuring adequate coverage of the measurement electrodes by the sample, however, is an important factor in achieving accurate test results. This has proven to be problematic in the past, particularly with the use of capillary fill spaces. Other examples of limitations to the accuracy of blood glucose measurements include variations in blood composition or state (other than the aspect being measured). For example, variations in hematocrit (concentration of red blood cells), or in the concentration of other chemicals in the blood, can effect the signal generation of a blood sample. Variations in the temperature of blood samples is yet another example of a confounding variable in measuring blood chemistry.
Thus, a system and method are needed that accurately measure blood glucose, even in the presence of confounding variables, including variations in temperature, hematocrit, and the concentrations of other chemicals in the blood. A system and method are also needed to ensure adequate coverage of the measurement electrodes by the sample, particularly in capillary fill devices. A system and method are likewise needed that accurately measure an analyte in a fluid. It is an object of the present invention to provide such a system and method.
SUMMARY OF THE INVENTION
In one form of the invention, a method of performing a measurement on a biological fluid in a test strip is disclosed, comprising: providing a biological fluid test strip including a capillary fill chamber extending a length along the test strip from an intake opening to a terminus, a first pair of electrodes in operative communication with the chamber, and a second pair of electrodes in operative communication with the chamber; dosing the test strip with a biological fluid effective to cause the biological fluid to flow from the intake opening toward the terminus; applying a first test signal to one of the first pair of electrodes; measuring a first response to the first test signal at the other of the first pair of electrodes; maintaining the first pair of electrodes in an inoperative state upon the measuring the first response; applying a second test signal to one of the second pair of electrodes; measuring a second response to the second test signal at the other of the second pair of electrodes; and performing a measurement upon the biological fluid after the measuring the second response.
In another form of the invention, a method of indicating acceptable fill time of a biological fluid in a test strip is disclosed, comprising: providing a biological fluid test strip including a capillary fill chamber extending a length along the test strip from an intake opening to a terminus, a first pair of electrodes in operative communication with the chamber, and a second pair of electrodes in operative communication with the chamber; dosing the test strip with a biological fluid effective to cause the biological fluid to flow from the intake opening toward the terminus; flowing a biological fluid from the opening toward the terminus; first determining when the biological fluid contacts the first electrodes; second determining when the biological fluid contacts the second electrodes; determining a fill time value based upon the first determining and the second determining; and comparing the fill time value to a predetermined value. BRIEF DESCRIPTION OF THE DRAWINGS
The invention will be further described, by way of example only, with reference to the accompanying drawings, in which:
Fig. 1 is a diagram of a first embodiment excitation signal suitable for use in a system and method according to the present invention, having a serially-applied AC component and DC component.
Fig. 2 is a diagram of a second embodiment excitation signal suitable for use in a system and method according to the present invention, having a simultaneously-applied AC component and DC component.
Figs. 3A-B illustrate a first embodiment test strip of the present invention.
Fig. 4 is a diagram of an excitation signal utilized in the test of Example 1.
Fig. 5 is a plot of the correlation coefficient r2 (glucose vs. DC current) versus Read Time for the test of Example 1 with no incubation time.
Fig. 6 is a plot of the correlation coefficient r2 (glucose vs. DC current) versus Read Time for the test of Example 1 with varying incubation time.
Fig. 7 is a plot of AC admittance versus hematocrit for the test of Example 2.
Fig. 8 is a plot of uncompensated DC current versus glucose for the test of Example 2.
Fig. 9 is a plot of the predicted glucose response versus the actual glucose response for the test of Example 2. Fig. 10 is a diagram of an excitation signal utilized in the test of Example 3.
Fig. 11 is a plot of the AC phase angle versus reference glucose for the test of Example 3.
Fig. 12 is a plot of the predicted glucose response versus the actual glucose response for the test of Example 3.
Fig. 13 is a diagram of an excitation signal utilized in the test of Example 4.
Fig. 14 is a plot of AC admittance versus hematocrit (parametrically displayed with temperature) for the test of Example 4.
Fig. 15 is a plot of the uncompensated DC response versus actual glucose for the test of Example 4.
Fig. 16 is a plot of the predicted glucose response versus actual glucose response for the test of Example 4.
Figs. 17A-B illustrate a second embodiment test strip of the present invention.
Fig. 18 is a plot parametrically illustrating the correlation coefficient r2 between the DC current response and glucose level as Read Time varies for three combinations of temperature and hematocrit in the test of Example 5.
Fig. 19 is a diagram of the excitation signal utilized in the test of Example 5.
Fig. 20 is a plot of AC admittance versus hematocrit as temperature is parametrically varied in the test of Example 5. Fig. 21 is a plot of AC admittance phase angle versus hematocrit as temperature is parametrically varied in the test of Example 5.
Fig. 22 is a plot of the uncompensated DC response versus actual glucose for the test of Example 5.
Fig. 23 is a plot of the predicted glucose response versus actual glucose response for the test of Example 5.
Fig. 24 is a diagram of the excitation signal utilized in the test of Example 6.
Fig. 25 is a plot of the correlation coefficient r2 between hematocrit and DC response current plotted against hematocrit in the test of Example 6.
Fig. 26 is a plot of AC admittance phase angle versus hematocrit for the test of Example 6.
Fig. 27 is a plot of the uncompensated DC response versus actual glucose for the test of Example 6.
Fig. 28 is a plot of the compensated DC response versus actual glucose for a 1.1 second Total Test Time of Example 6.
Fig. 29 is a plot of the compensated DC response versus actual glucose for a 1.5 second Total Test Time of Example 6.
Fig. 30 is a plot of the compensated DC response versus actual glucose for a 1.9 second Total Test Time of Example 6.
Fig. 31 is a table detailing the heights and widths of the capillary fill channels used in the test devices of Example 8, as well as schematic diagrams of convex and concave sample flow fronts in a capillary fill space. Figs. 32A-C are schematic plan views of a test strip illustrating the potential for biased measurement results when a concave flow front encounters a prior art dose sufficiency electrode.
Fig. 33 is a schematic plan view of a test strip of the present invention having a pair of perpendicular dose sufficiency electrodes that are independent from the measurement electrodes.
Figs. 34A-B are schematic plan views of the test strip of FIG. 33 containing samples with convex and concave flow fronts, respectively.
Figs. 35A-B are schematic plan views of a test strip of the present invention having a pair of parallel dose sufficiency electrodes that are independent from the measurement electrodes.
Fig. 36 is a schematic plan view of the test strip of Fig. 35, schematically illustrating the electric field lines that communicate between the electrode gap when the electrodes are covered with sample.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
For the purposes of promoting an understanding of the principles of the invention, reference will now be made to the embodiment illustrated in the drawings, and specific language will be used to describe that embodiment. It will nevertheless be understood that no limitation of the scope of the invention is intended. Alterations and modifications in the illustrated device, and further applications of the principles of the invention as illustrated therein, as would normally occur to one skilled in the art to which the invention relates are contemplated, are desired to be protected. In particular, although the invention is discussed in terms of a blood glucose meter, it is contemplated that the invention can be used with devices for measuring other analytes and other sample types. Such alternative embodiments require certain adaptations to the embodiments discussed herein that would be obvious to those skilled in the art.
The entire disclosure of U.S. provisional applications titled DEVICES AND METHODS RELATING TO ELECTROCHEMICAL BIOSENSORS (Serial No. 60/480,243, filed June 20, 2003) and DEVICES AND METHODS RELATING TO ANALYTE SENSOR (Serial No. 60/480,397, Filed June 20, 2003) are hereby incorporated by reference in their entireties.
A system and method according to the present invention permit the accurate measurement of an analyte in a fluid. In particular, the measurement of the analyte remains accurate despite the presence of interferants, which would otherwise cause error. For example, a blood glucose meter according to the present invention measures the concentration of blood glucose without error that is typically caused by variations in the temperature and the hematocrit level of the sample. The accurate measurement of blood glucose is invaluable to the prevention of blindness, loss of circulation, and other complications of inadequate regulation of blood glucose in diabetics. An additional advantage of a system and method according to the present invention is that measurements can be made much more rapidly and with much smaller sample volumes, making it more convenient for the diabetic person to measure their blood glucose. Likewise, accurate and rapid measurement of other analytes in blood, urine, or other biological fluids provides for improved diagnosis and treatment of a wide range of medical conditions.
It will be appreciated that electrochemical blood glucose meters typically (but not always) measure the electrochemical response of a blood sample in the presence of a reagent. The reagent reacts with the glucose to produce charge carriers that are not otherwise present in blood. Consequently, the electrochemical response of the blood in the presence of a given signal is intended to be primarily dependent upon the concentration of blood glucose. Secondarily, however, the electrochemical response of the blood to a given signal is dependent upon other factors, including hematocrit and temperature. See, for example, U.S. Patents Nos. 5,243,516; 5,288,636; 5,352,351; 5,385,846; and 5,508,171, which discuss the confounding effects of hematocrit on the measurement of blood glucose, and which are hereby incoφorated by reference in their entireties. In addition, certain other chemicals can influence the transfer of charge carriers through a blood sample, including, for example, uric acid, bilirubin, and oxygen, thereby causing error in the measurement of glucose.
A preferred embodiment system and method for measuring blood glucose according to the present invention operates generally by using the signal- dependence of the contribution of various factors to the impedance (from which admittance and phase angle may be derived) of a blood sample. Because the contribution of various factors to the impedance of a blood sample is a function of the applied signal, the effects of confounding factors (that is, those other than the factors sought to be measured) can be substantially reduced by measuring the impedance of the blood sample to multiple signals. In particular, the effects of confounding factors, (primarily temperature and hematocrit, but also including chemical interferants such as oxygen), contribute primarily to the resistivity of the sample, while the glucose-dependent reaction contributes primarily to the capacitance. Thus, the effects of the confounding factors can be eliminated by measuring the impedance of the blood sample to an AC excitation, either alone or in combination with a DC excitation. The impedance (or the impedance derived admittance and phase information) of the AC signal is then used to correct the DC signal or AC derived capacitance for the effects of interferants. It will be appreciated that measurements at sufficiently high AC frequencies are relatively insensitive to the capacitive component of the sample's impedance, while low frequency (including DC) measurements are increasingly (with decreasing frequency) sensitive to both the resistive and the capacitive components of the sample's impedance. The resistive and capacitive components of the impedance can be better isolated by measuring the impedance at a larger number of frequencies. However, the cost and complexity of the meter increases as the number of measurements increases and the number of frequencies that need to be generated increases. Thus, in the presently preferred embodiment, the impedance may be measured at greater than ten frequencies, but preferably at between two and ten frequencies, and most preferably at between two and five frequencies.
As used herein, the phrase "a signal having an AC component" refers to a signal which has some alternating potential (voltage) portions. For example, the signal may be an "AC signal" having 100% alternating potential (voltage) and no DC portions; the signal may have AC and DC portions separated in time; or the signal may be AC with a DC offset (AC and DC signals superimposed).
Sample Measurement with Successive AC and DC Signals
Figure 1 illustrates a preferred embodiment excitation signal suitable for use in a system and method according to the present invention, indicated generally at 100, in which DC excitation and four frequencies of AC excitation are used. Figure 1 also illustrates a typical response to the excitation when the excitation is applied to a sample of whole blood mixed with an appropriate reagent, the response indicated generally at 102. A relatively high frequency signal is applied, starting at time 101. In the preferred embodiment the frequency is between about lOkHz and about 20kHz, and has an amplitude between about 12.4mV and about 56.6mV. A frequency of 20kHz is used in the example of FIG. 1. Those skilled in the art will appreciate that these values may be optimised to various parameters such as cell geometry and the particular cell chemistry. At time 110 a test strip is inserted into the meter and several possible responses to the insertion of the test strip into the glucose meter are shown. It will be appreciated that the test strip may also be inserted before the excitation signal 100 is initiated (i.e. before time 101); however, the test strip itself may advantageously be tested as a control for the suitability of the strip. It is therefore desirable that the excitation signal 100 be initiated prior to test strip insertion. For example, relatively large current leakage, as shown at 112, may occur if the strip is wet, either because the test strip was pre-dosed, or due to environmental moisture. If the test strip has been pre-dosed and permitted to largely or completely dry out, an intermediate current leakage may occur, as shown at 114. Ideally, insertion of the test strip will cause no or negligible leakage current due to an expected absence of charge carriers between the test electrodes, as shown at 116. Measured current leakage above a predetermined threshold level will preferably cause an error message to be displayed and prevent the test from continuing.
Once a suitable test strip has been inserted, the user doses the strip, as shown at time 120. While the blood sample is covering the electrodes the current response will rapidly increase, as the glucose reacts with the reagent and the contact area increases to maximum. The response current will reach a stable state, which indicates the impedance of the sample at this frequency. Once this measurement is made and recorded by the test meter, the excitation frequency is then stepped down to about 10kHz in the preferred embodiment, as shown at time 130. Another measurement is made and recorded by the test meter, and the frequency is stepped down to about 2kHz in the preferred embodiment, as shown at 140. A third measurement is made and recorded by the test meter at this frequency. A fourth measurement is made at about 1kHz in the preferred embodiment, as shown at 150. In the preferred embodiment, measurements are taken at regular intervals (e.g. 10 points per cycle). It will be appreciated that the stable state response may be measured as current or voltage (preferably both magnitude and phase) and the impedance and/or admittance can be calculated therefrom. Although the present specification and claims may refer alternately to the AC response as impedance or admittance (magnitude and/or phase), resistance, conductivity, current or charge, and to the DC response as current, charge, resistance or conductivity, those skilled in the art will recognize that these measures are interchangeable, it only being necessary to adjust the measurement and correction mathematics to account for which measure is being employed. In the preferred embodiment, the test meter applies a voltage to one electrode and measures the current response at the other electrode to obtain both the AC and DC response.
In certain alternative embodiments measurements are made at fewer or more frequencies. Preferably measurements are made at at least two AC frequencies at least an order of magnitude apart. If more than two AC frequencies are used, then it is preferable that the highest and lowest frequencies be at least an order of magnitude apart.
It will be appreciated that various waveforms may be used in an AC signal, including, for example, sinusoidal, trapezoidal, triangle, square and filtered square. In the presently preferred embodiment the AC signal has a filtered square waveform that approximates a sine wave. This waveform can be generated more economically than a true sine wave, using a square wave generator and one or more filters.
Once all four AC measurements are made, the signal is preferably briefly reduced to zero amplitude, as shown at 160. The DC excitation is then begun, as shown at 170. The amplitude of the DC excitation is advantageously selected based on the reagent being used, in order to maximise the resulting response or response robustness. For example, if ferricyanide is being used in a biamperometry system, the DC amplitude is preferably about 300mV. For another example, if a nitrosoaniline derivative is being used in a biamperometry system, the DC amplitude is preferably about 500-550mV. In the alternative, if a third reference electrode is used, the DC applitude is preferably 600 mV (versus the silver/silver chloride reference electrode) for ferricyanide, and 40-100 mV (versus the silver/silver chloride reference electrode) for nitrosoaniline derivative. During DC excitation, measurements are preferably made at a rate of 100 pts/sec. The current response will follow a decay curve (known as a Cottrell curve), as the reaction is limited by the diffusion of unreacted glucose next to the working electrode. The resulting stable-state amplitude (measured or projected) is used to determine a glucose estimation of the sample, as is known in the art. A corrected estimation is then determined that corresponds more closely to the concentration of glucose in the blood, by using the impedance of the sample to the AC signal to correct for the effects of interferants, as explained in greater detail hereinbelow.
It will be appreciated that a method according to the present invention may also be used to measure the concentration of other analytes and in other fluids. For example, a method according to the present invention may be used to measure the concentration of a medically significant analyte in urine, saliva, spinal fluid, etc. Likewise, by appropriate selection of reagent a method according to the present invention may be adapted to measure the concentration of, for example, lactic acid, hydroxybutyric acid, etc.
Sample Measurement with Simultaneously Applied AC and DC Signals
It will be appreciated that at least some of the applied DC and AC components can also be applied simultaneously. Figure 2 illustrates an excitation signal suitable for use in a system and method according to the present invention in which some of the AC and DC components are applied simultaneously, indicated generally at 200, and having corresponding events numbered correspondingly to Figure 1 (so, for example, the signal 200 is initiated at time 201, and a strip is inserted at time 210, etc.). As with the signal 100, the signal 200 has a frequency of about 10-20kHz and an amplitude of about 12.4-56.6m However, after the strip has been dosed, as shown at time 220, a DC offset is superimposed, as shown at 270. Typical AC and DC responses are shown in Figure 2. The AC and DC responses are measured simultaneously and mathematically deconvoluted and used to determine the impedance (admittance magnitude and phase) and the amperometric or coulometric response.
A system for measuring blood glucose according to the present invention advantageously employs a blood glucose meter and test strips generally similar to those used in prior art systems, such as those commercially available from Roche Diagnostics, and such as are described in U.S. Patents Nos. 6,270,637; and 5,989,917, which are hereby incorporated in their entireties. These test strips provide apparati having a sample cell in which the blood sample is received for testing, and electrodes disposed within the sample cell through which the excitation signal is provided and the measurements are made. Those skilled in the art will appreciate that these test strips and meters may advantageously be used for the measurement of glucose in blood, but that other apparati may be more suitable for the measurement of other analytes or other biological fluids when practising the present invention.
A suitable glucose meter may be adapted from such known meters by the addition of electronic circuitry that generates and measures signals having AC and DC components, such as those described hereinabove, and by being programmed to correct the DC measurement using the AC measurement(s), as described in greater detail hereinbelow. It will be appreciated that the specific geometry and chemistry of the test strips can cause variations in the relationships between the concentration of glucose, hematocrit, and temperature, and the impedance of a sample. Thus, a given combination of test strip geometry and chemistry must be calibrated, and the meter programmed with the corresponding algorithm. The present invention comprehends the application of excitation signals in any order and combination. For example, the present invention comprehends the application of 1) AC only, 2) AC then DC, 3) AC then DC then AC, 4) DC then AC, and 5) AC with a DC offset, just to name a few of the possible permutations.
The use of the complex AC impedance measurement data to correct for the effects of interferants on the DC measurement is advantageously illustrated by the following series of examples. These examples illustrate how the principles of the present invention can facilitate improvements in accuracy and test speed when measuring the concentration of an analyte in a test specimen. Although the following examples deal with correcting for the interfering effects of hematocrit and temperature on blood glucose determinations, those skilled in the art will recognize that the teachings of the present invention are equally useful for correcting for the effects of other interferants in both blood glucose measurements and in the measurement of other analytes. Furthermore, the present specification and claims refer to steps such as "determine the hematocrit value" and "determine the temperature," etc. To use the hematocrit value as an example, it is intended that such statements include not only determining the actual hematocrit value, but also a hematocrit correction factor vs. some nominal point. In other words, the process may never actually arrive at a number equal to the hematocrit value of the sample, but instead determine that the sample's hematocrit differs from a nominal value by a certain amount. Both concepts are intended to be covered by statements such as "determine the hematocrit value."
Example 1: DC-Only Measurement Dose Response Study
The measurements made in Example 1 were achieved using the test strip illustrated in Figures 3A-B and indicated generally at 300. The test strip 300 includes a capillary fill space containing a relatively thick film reagent and working and counter electrodes, as described in U.S. Patent No. 5,997,817, which is hereby incorporated by reference. The test strip 300 is commercially available from Roche Diagnostics Corporation (Indianapolis, DN) under the brand name Comfort Curve ®. The ferricyanide reagent used had the composition described in Tables I and II.
Table I: Reagent Mass Composition - Prior to Dispense and Drying
Figure imgf000018_0001
Figure imgf000019_0001
% Solids 0.1352687
Target pH 6.8
Specific Enzyme Activity Used (U/mg) 689 DCIP
Dispense Volume per Sensor 4.6 mg
Table J: Reagent Layer Composition - After Drying
Figure imgf000019_0002
In the measurements, blood samples were applied to test strip 300 and the excitation potentials illustrated in Figure 4 were applied to the electrodes. The excitation comprised a 2 kHz 40 mV-ms (56.56 mV peak) AC signal applied between 0 seconds and approximately 4.5 seconds after sample application, followed by a 300 mV DC signal applied thereafter. For the calculations of this example, however, only the DC measurement data was analyzed.
In order to determine the minimum needed DC excitation time, a "dose response" study was performed, in which glycollyzed (glucose depleted) blood was divided into discrete aliquots and controlled levels of glucose were added to obtain five different known levels of glucose in the blood samples. The resulting DC current profile was then examined as two parameters were varied. The first parameter was the Incubation Time, or the time between the detection of the blood sample being applied to the test strip 300 and the application of the DC potential to the test strip 300. The second parameter to be varied was the Read Time, or the time period after application of the DC potential and the measurement of the resulting current. The length of time between detection of the blood sample being applied to the test strip to the taking of the last measurement used in the concentration determination calculations is the Total Test Time. In this study, therefore, the sum of the Incubation Time and the Read Time is the Total Test Time. The results of this study are illustrated in Figures 5 and 6.
In Figure 5, the DC response was measured with no incubation time (Read Time = Total Test Time). Figure 5 plots the correlation coefficient r2 versus Read Time. As can be seen, the correlation exceeds 0.95 within 1.0 second. In Figure 6, the DC response was measured with varying Incubation Time. When an Incubation Time is provided (even an Incubation Time as short as two (2) seconds), the r2 value rose to over 0.99 in 0.5 seconds or less after application of the DC potential.
The barrier to implementation of such fast test times in a consumer glucose test device, however, is the variation from blood sample to blood sample of the level of interference from the presence of blood cells in the sample. The hematocrit (the percentage of the volume of a blood sample which is comprised of cells versus plasma) varies from individual to individual. The interference effect of hematocrit on such measurements is fairly complex. In the tests of Example 1, however, all samples contained the same level of hematocrit. With no variable hematocrit influence at the different glucose levels, the hematocrit term cancels out in the correlation figures.
Example 2: Combined AC and DC Measurement of Capillary Blood Samples
The measurements made in Example 2 were also achieved using the test strip illustrated in Figures 3A-B and indicated generally at 300. As described above, the test strip 300 includes a capillary fill space containing a relatively thick film reagent and working and counter electrodes, as described in U.S. Patent No. 5,997,817, which is hereby incoφorated herein by reference.
In the measurements, capillary blood samples from various fingerstick donors were applied to test strip 300 and the excitation potentials illustrated in Figure 4 were applied to the electrodes. The excitation comprised a 2 kHz 40 rnVrms AC signal applied between 0 seconds and approximately 4.5 seconds after sample application, followed by a 300 mV DC signal applied thereafter. In this Example 2, the AC response of the sample was derived as admittance (the inverse of impedance). The admittance response is proportionate to the hematocrit level of the sample in a temperature dependent manner. The relationship between admittance, hematocrit and testing temperature is illustrated in Figure 7. The data used for the admittance charted in Figure 7 is the last admittance measurement made for each sample during the AC portion of the excitation illustrated in Figure 4. Regression analysis of this data allows admittance, hematocrit and temperature to be related according to the following formula:
HeSt = c0 + c1Y2kHz + c2dT (Equation 1)
Using this relationship to predict the blood hematocrit is accomplished using test temperature data reported by the temperature sensor in the meter and the measured admittance. In Equation 1, c0, Ci and c2 are constants, dϊ is the deviation in temperature from a center defined as "nominal" (24°C for example), and HeSt is the estimated deviation in hematocrit from a similar "nominal" value. For the present puφoses, the actual hematocrit value is not necessary, and it is generally preferred to produce a response which is proportionate but centers around a nominal hematocrit. Thus, for a 70% hematocrit, the deviation from a nominal value of
42% would be 28%, while conversely for a 20% hematocrit the deviation from that same nominal value would be -22%.
By using the AC admittance measurement to estimate the hematocrit level using Equation 1, the accuracy of the DC glucose response can be greatly improved by combining the estimated hematocrit, temperature and DC response to correct for the hematocrit interference in the DC response as follows:
PRED = (ao + hctiHest + hct2HeSt 2 + taui-TT + tau2-fT2) (Equation 2)
+ (a1DC)(l + hct3HeSt + hct4HeSt 2)(l + tau3dT + tau4dT2)
where DC is the measured glucose current response to the applied DC signal and PRED is the compensated (predicted) glucose response corrected for the effects of hematocrit and temperature. The constants (ao, hct], hct2, tau1; tau2) a], hct3? hct4, tau3 and tau4) in Equation 2 can be determined using regression analysis, as is known in the art.
Figure 8 illustrates the uncompensated 5.5 second DC glucose response of all of the capillary blood samples as temperature varies (ignoring the AC measurement data). As will be appreciated, there is a wide variation in the DC current response as temperature and hematocrit vary. Figure 9 illustrates the correlation between the actual blood glucose level of the sample versus the predicted response using Equation 2. As can be seen, when the DC response is compensated for hematocrit levels using the AC response data, r2 values of 0.9404 to 0.9605 are achieved with a Total Test Time of 5.5 seconds. Example 3: Use of AC Phase Angle to Estimate Blood Glucose Levels and Hematocrit
The measurements made in Example 3 were also achieved using the test strip illustrated in Figures 3A-B and indicated generally at 300. As described above, the test strip 300 includes a capillary fill space containing a relatively thick film reagent and working and counter electrodes, as described in U.S. Patent No. 5,997,817, which is hereby incoφorated by reference. Because hematocrit levels from capillary blood samples typically vary only between 30% - 50%, spiked venous blood samples having a hematocrit range from 20% - 70% were used for this Example 3. Five levels of glucose, temperature (14, 21, 27, 36 and 42 °C) and hematocrit (20, 30, 45, 60 and 70%) were independently varied, producing a covariance study with 125 samples. In the measurements, blood samples were applied to test strip 300 and the excitation potentials illustrated in Figure 10 were applied to the electrodes. The excitation comprised a 2 kHz AC signal for approximately 4.1 seconds, a 1 kHz AC signal for approximately 0.1 seconds, and a 200 Hz signal for approximately 0.1 seconds. All three AC signals had an amplitude of 56.56 mV peak. No DC excitation was used in this example. The Total Test Time was 4.3 seconds from sample application time.
It was found that another component of the AC response, the phase angle (particularly at lower frequencies, such as 200 Hz in this Example 3), is also a function of the sample glucose level in the case of this test strip and reagent. This relationship is demonstrated in Figure 11, where the AC phase angle for each of the three test frequencies is plotted versus the reference glucose level. Regression analysis for each of the three frequencies produces AC phase angle-to-reference glucose level r2 correlation values of 0.9114 at 2 kHz, 0.9354 at 1 kHz, and 0.9635 at 200 Hz. The present invention therefore comprehends the use of the AC phase angle to measure glucose levels. The AC excitation frequency producing the measured phase angle is preferably 2 kHz or below, more preferably 1 kHz or below, and most preferably 200 Hz or below, but not including DC excitation. The linearized relationship between the 200 Hz phase angle response and the blood glucose level is as follows:
Peff = (Φ200 HZ / T ) (Equation 3)
where Peβ is the effective phase, which is proportional to glucose, the terms T and γ are constants, and Φ is the measured AC phase angle.
Using the same approach to compensate for temperature and hematocrit as used in Example 1 above (see Equations 1 and 2) produced a predictive algorithm as follows:
PRED = (ao + hctiHest + hct2HeSt 2 + taui- T + tau2dT2) (Equation 4)
+ (aιPeff)(l + hct3HeSt + hct4HeSt 2)(l + tau3dT + tau4-fT2)
The resulting compensated (predicted) response PRED versus glucose for the 125 blood samples (each tested with eight test strips) is shown in Figure 12. The r2 correlation of the PRED response vs. known glucose level, where all temperatures and all hematocrits are combined, is 0.9870. This Example 3 demonstrates again the value of AC measurements for compensating for interferants that reduce the accuracy of blood glucose measurements. Using an existing commercially available sensor, the present invention yields a 4.3 second Total Test Time with an overall r2 of 0.9870.
It was also determined that AC phase angle measurements can produce hematocrit level measurements that are almost immune to the effects of temperature variation. In another covariant study of 125 samples (five glucose concentrations, five hematocrit concentrations and five temperatures), each of the samples was tested using an excitation profile of 20 kHz, 10kHz, 2 kHz, 1kHz and DC. The AC phase angle at various frequencies was related to glucose, hematocrit and temperature using linear regression to determine the coefficients of the following formula at each of the four AC frequencies: Phase = c0 + cjGlu + c2HCT + c3Temp (Equation 5)
where Glu is the known glucose concentration, HCT is the known hematocrit concentration and Temp is the known temperature. The determined coefficients revealed that the temperature coefficient (c3) was essentially zero at 20 kHz and 10 kHz, cancelling temperature from the equation at these frequencies. Furthermore, the glucose coefficient (c is essentially zero at all of the AC frequencies because, as explained hereinabove, the higher frequency AC impedance measurements are largely unaffected by glucose levels and are therefore useful for measuring the levels of interfering substances. It was therefore found that the hematocrit level could be determined independent of temperature and glucose level using only the AC phase angle measurements. In a preferred embodiment, the hematocrit may be measured using the phase angle data from all four measured frequencies:
Hest = Co + c1Φ20kHz + c2ΦιokHz + c3Φ2kHz + c4ΦlkHz (Equation 6)
Those skilled in the art will recognise that that the coefficients can be empirically determined for any particular test strip architecture and reagent chemistry. The present invention therefore may be used to estimate hematocrit using only AC phase angle measurements preferably made at at least one AC frequency, more preferably made at at least two AC frequencies, and most preferably made at at least four AC frequencies.
Example 4: Combined AC and DC Measurement Using Nitrosoaniline Reagent
The measurements made in Example 4 were also achieved using the test strip illustrated in Figures 3A-B and indicated generally at 300. As described above, the test strip 300 includes a capillary fill space containing a relatively thick film reagent and working and counter electrodes, as described in U.S. Patent No. 5,997,817, which is hereby incoφorated by reference. The test strip was modified from that described in U.S. Patent No. 5,997,817, however, by the use of a different reagent. The nitrosoaniline reagent used had the composition described in Tables III and IV.
Table III: Reagent Mass Composition - Prior to Dispense and Drying
Figure imgf000026_0001
% Solids 0.1352687
Target pH 6.8
Specific Enzyme Activity Used (U/mg) 689 DCIP
Dispense Volume per Sensor 4.6 mg Table IV: Reagent Layer Composition - After Drying
Figure imgf000027_0001
The method for the manufacture of the glucose biosensor for this Example
4 is the same in all respects as disclosed in U.S. Patent No. 5,997,817 except for the manufacture of the reagent. A protocol for the preparation of the preferred embodiment nitrosoaniline reagent is as follows:
Step 1: Prepare a buffer solution by adding 1.54g of dibasic potassium phosphate (anhydrous) to 43.5 g of deionized water. Mix until the potassium phosphate is dissolved.
Step 2: To the solution from step 1, add 1.14g of monobasic potassium phosphate and mix until dissolved. Step 3: To the solution from step 2, add 0.59g of disodium succinate (hexahydrate) and mix until dissolved.
Step 4: Verify that the pH of the solution from step 3 is 6.7 +/- 0.1. Adjustment should not be necessary.
Step 5: Prepare a 5g aliquot of the solution from step 4, and to this add 113 kilounits (by DCIP assay) of the apoenzyme of quinoprotein glucose dehydrogenase (EC#: 1.1.99.17). This is approximately 0.1646g. Mix, slowly, until the protein is dissolved.
Step 6: To the solution from step 5, add 4.2 milligrams of PQQ and mix for no less than 2 hours to allow the PQQ and the apoenzyme to reassociate in order to provide functional enzyme.
Step 7: To the solution from step 4, add 0.66g of the mediator precursor, N,N- bis(hydroxyethyl)-3-methoxy-4-nitrosoaniline (hydrochloride) (BM 31.1144). Mix until dissolved (this solution will have a greenish black coloration).
Step 8: Measure the pH of the solution from step 7 and adjust the pH to a target of 7.0 +/- 0.1. Normally this is accomplished with 1.197g of 5N potassium hydroxide. Because the specific amount of potassium hydroxide may vary as needed to reach the desired pH, generally deviations in mass from the 1.197g are made up from an aliquot of 3.309g deionized water which is also added at this step.
Step 9: Prepare a solution of Natrosol 250M (available from Aqualon), by slowly sprinkling 0.047g over 44.57g of deionized water which is mixed (using a rotary mixer and blade impeller) at a rate of approximately 600 φm in a vessel of sufficient depth such that the rotor blades are not exposed nor the solution running over. Mix until the Natrosol is completely dissolved. Step 10: Prepare a suspension of Avicel RC-591F (available from FMS), by slowly sprinkling 0.54g onto the surface of the solution from step 9, mixing at a rate of approximately 600 φm for not less than 60 minutes before proceeding.
Step 11: To the suspension from step 10, gradually add 0.8 lg of Polyethylene oxide of 300kDa mean molecular weight while mixing and continue to mix for not less than 60 minutes before proceeding.
Step 12: Gradually add the solution from step 8 to the suspension from step 11 while mixing. Reduce the mixing rate to 400 φm.
Step 13: To the reagent from step 12, add 1.89g of Trehalose and continue mixing for not less than 15 minutes.
Step 14: To the reagent from step 13, add 32.7mg of Triton X-100 (available from Roche Diagnostics) and continue mixing.
Step 15: To the reagent from step 14, add the enzyme solution from step 6. Mix for no less than 30 minutes. At this point the reagent is complete. At room teperature the wet reagent mass is considered acceptable for use for 24 hours.
Spiked venous blood samples were used. Five levels of glucose, four temperatures (19, 23, 32 and 38 °C) and five levels of hematocrit (20, 30, 45, 60 and 70%) were independently varied, producing a covariance study with 100 samples. 16 test strips 300 were tested for each unique combination of glucose, temperature and hematocrit. The blood samples were applied to test strip 300 and the excitation potentials illustrated in Figure 13 were applied to the electrodes. The excitation comprised a 3.2 kHz AC signal for approximately 4.0 seconds, a 2.13 kHz AC signal for approximately 0.1 seconds, a 1.07 kHz AC signal for approximately 0.1 seconds, a 200 Hz AC signal for approximately 0.1 seconds, a 25 Hz AC signal for approximately 0.1 seconds, followed by a DC signal of 550 mV for approximately 1.0 second. All four AC signals had an amplitude of 56.56 mV peak. The Total Test Time was 5.5 seconds from sample application time.
In this Example 4, the AC response of the sample was derived as admittance (the inverse of impedance). The admittance response is proportionate to the hematocrit level of the sample in a temperature dependent manner. The relationship between admittance, hematocrit and testing temperature is illustrated in Figure 14. As compared to the test strip architecture of Example 2, the orthogonality of the temperature and hematocrit influence on glucose was not as strong in this Example 4, therefore a cross product term (T x HCT) was added to the admittance regression formula used in Figure 14. The data used for the admittance charted in Figure 14 is the last admittance measurement made for each sample during the 3.2 kHz AC portion of the excitation illustrated in Figure 13.
Regression analysis of this data allows admittance, hematocrit and temperature to be related according to the following formula:
Hest = (Y3.2kHz + Co + Ci-iT)/(c2crr + c3) (Equation 7)
It was determined that the admittance measurement made at 3.2 kHz was best correlated with hematocrit for this test system. Using this relationship to predict the blood hematocrit is accomplished using test temperature data reported by the temperature sensor in the meter and the measured admittance. In Equation 7, Co, Ci, c2 and c3 are constants, dT is the deviation in temperature from a center defined as "nominal" (24°C for example), and HeSt is the estimated deviation in hematocrit from a similar "nominal" value. For the present puφoses, the actual hematocrit value is not necessary, and it is generally preferred to produce a response which is proportionate but centers around a nominal hematocrit. Thus, for a 70% hematocrit, the deviation from a nominal value of 42% would be 28%, while conversely for a 20% hematocrit the deviation from the same nominal value would be -22%. By using the AC admittance measurement to estimate the hematocrit level using Equation 7, the accuracy of the DC glucose response can be greatly improved by combining the estimated hematocrit, temperature and DC response to correct for the hematocrit interference in the DC response as follows (same as Equation 2 above):
PRED = (ao + hctiHest + hct2HeSt 2 + tauidT + tau2dT2) (Equation 8)
+ (aiDC)(l + hct3HeSt + hct HeSt 2)(l + tau3- T + tau4dT2)
The constants in Equation 8 can be determined using regression analysis, as is known in the art.
Figure 15 illustrates the uncompensated 5.5 second DC glucose response of all of the blood samples as hematocrit and temperature vary (ignoring the AC measurement data). As will be appreciated, there is a wide variation in the DC current response as temperature and hematocrit vary. Figure 16 illustrates the correlation between the actual blood glucose level of the sample versus the predicted response using Equation 8. As can be seen, when the DC response is compensated for hematocrit levels using the AC response data, an overall r2 value of 0.9818 is achieved with a Total Test Time of 5.5 seconds. This demonstrates the applicability of the present invention in achieving high accuracy and fast test times with a different reagent class than was used in Examples 1-3.
Example 5: Combined AC and DC Measurement Using a 0.397 μl Sample
The measurement methods of the present invention have been found to be useful with other test strip designs as well. Example 5 was conducted using the test strip design illustrated in Figures 17A-B, and indicated generally at 1700. Referring to Figure 17 A, the test strip 1700 comprises a bottom foil layer 1702 formed from an opaque piece of 350 μm thick polyester (in the preferred embodiment this is Melinex 329 available from DuPont) coated with a 50 nm conductive (gold) layer (by sputtering or vapor deposition, for example). Electrodes and connecting traces are then patterned in the conductive layer by a laser ablation process to form working, counter, and dose sufficiency electrodes (described in greater detail hereinbelow) as shown. The laser ablation process is performed by means of an excimer laser which passes through a chrome-on-quartz mask. The mask pattern causes parts of the laser field to be reflected while allowing other parts of the field to pass through, creating a pattern on the gold which is ejected from the surface where contacted by the laser light.
Examples of the use of laser ablation techniques in preparing electrodes for biosensors are described in United States Patent Application Serial Number 09/866,030, "Biosensors with Laser Ablation Electrodes with a Continuous Coveriay Channel" filed May 25, 2001, and in United States Patent Application Serial Number 09/411 ,940, entitled "Laser Defined Features for Patterned Laminates and Electrode," filed October 4, 1999, both disclosures incoφorated herein by reference.
The bottom foil layer 1702 is then coated in the area extending over the electrodes with a reagent layer 1704 in the form of an extremely thin reagent film. This procedure places a stripe of approximately 7.2 millimeters width across the bottom foil 1702 in the region labelled "Reagent Layer" on Figure 17. In the present Example, this region is coated at a wet-coat weight of 50 grams per square meter of coated surface area leaving a dried reagent less than 20 μm thick. The reagent stripe is dried conventionally with an in-line drying system where the nominal air temperature is at 110°C. The rate of processing is nominally 30-38 meters per minute and depends upon the rheology of the reagent.
The materials are processed in continuous reels such that the electrode pattern is orthogonal to the length of the reel, in the case of the bottom foil 1702. Once the bottom foil 1702 has been coated with reagent, the spacer is slit and placed in a reel-to-reel process onto the bottom foil 1702. Two spacers 1706 formed from 100 μm polyester (in the preferred embodiment this is Melinex 329 available from DuPont) coated with 25 μm PSA (hydrophobic adhesive) on both the dorsal and ventral surfaces are applied to the bottom foil layer 1702, such that the spacers 1706 are separated by 1.5 mm and the working, counter and dose sufficiency electrodes are centered in this gap. A top foil layer 1708 formed from 100 μm polyester coated with a hydrophilic film on its ventral surface (using the process described in U.S. Patent No. 5, 997,817) is placed over the spacers 1706. In the preferred embodiment, the hydrophilic film is coated with a mixture of Vitel and Rhodapex surfactant at a nominal thickness of 10 microns. The top foil layer 1708 is laminated using a reel-to-reel process. The sensors can then be produced from the resulting reels of material by means of slitting and cutting.
The 1.5 mm gap in the spacers 1706 therefore forms a capillary fill space between the bottom foil layer 1702 and the top foil layer 1708. The hydrophobic adhesive on the spacers 1706 prevents the test sample from flowing into the reagent under the spacers 1706, thereby defining the test chamber volume. Because the test strip 1700 is 5 mm wide and the combined height of the spacer 1706 and conductive layer is 0.15 mm, the sample receiving chamber volume is
5 mm x 1.5 mm x 0.15 mm = 1.125 μl (Equation 9)
As shown in Figure 17B, the distance from the sample application port
1710 and the dose sufficiency electrodes is 1.765 mm. The volume of sample needed to sufficiently cover the working, counter and dose sufficiency electrodes (i.e. the minimum sample volume necessary for a measurement) is
1.5 mm x 1.765 mm x 0.15 mm = 0.397 μl (Equation 10)
The reagent composition for the test strip 1700 is given in Tables V and VI.
Table V: Reagent Mass Composition - Prior to Dispense and Drying
Figure imgf000033_0001
Figure imgf000034_0001
% Solids 6.6585%
Target pH 7
Specific Enzyme Activity Used (U/mg) 689 DCIP
Wet Reagent Coat Weight per Sensor (ug/mm2) 50
Table VI: Reagent Layer Composition - After Drying
Figure imgf000034_0002
Figure imgf000035_0001
* "Mass per Sensor" is the amount of the component within the capillary; this does not reflect the reagent that is outside of the capillary.
A protocol for the preparation of the preferred embodiment nitrosoaniline reagent is as follows:
Step 1: Prepare a buffer solution by adding 1.654g of dibasic potassium phosphate (trihydrous) to 31.394 g of deionized water. Mix until the potassium phosphate is dissolved.
Step 2: To the solution from step 1, add 0.941g of monobasic potassium phosphate and mix until dissolved.
Step 3: To the solution from step 2, add 0.285g of disodium succinate (hexahydrate) and mix until dissolved.
Step 4: Verify that the pH of the solution from step 3 is 6.8 +/- 0.1. Adjustment should not be necessary.
Step 5: Prepare a 4.68g aliquot of the solution from step 4, and to this add 229 kilounits (by DCIP assay) of the apoenzyme of quinoprotein glucose dehydrogenase (EC#: 1.1.99.17). This is approximately 0.3321g. Mix, slowly, until the protein is dissolved.
Step 6: To the solution from step 5, add 9.3 milligrams of PQQ and mix for no less than 2 hours to allow the PQQ and the apoenzyme to reassociate in order to provide functional enzyme. Step 7: Prepare a solution by dissolving 0.772g of Trehalose into 1.218g of deionized water.
Step 8: After enzyme reassociation, add the solution from step 7 to the solution from step 6 and continue mixing for not less than 30 minutes.
Step 9: To the solution from step 4, add 0.690g of the mediator precursor BM 31.1144. Mix until dissolved (this solution will have a greenish black coloration).
Step 10: Measure the pH of the solution from step 9 and adjust the pH to a target of 7.0 +/- 0.1. Normally this is accomplished with 1.006g of 5N potassium hydroxide. Because the specific amount of potassium hydroxide may vary as needed to reach the desired pH, generally deviations in mass from the 1.006g are made up from an aliquot of 3.767g deionized water which is also added at this step.
Step 11 : Prepare a solution of Natrosol 250M (available from Aqualon), by slowly sprinkling 0.350g over 56.191g of deionized water which is mixed (using a rotary mixer and blade impeller) at an initial rate of approximately 600 φm in a vessel of sufficient depth such that the rotor blades are not exposed nor the solution running over. As the Natrosol dissolves, the mixing rate needs to be increased to a speed of 1.2 - 1.4 kφm. Mix until the Natrosol is completely dissolved. Note that the resulting matrix will be extremely viscous - this is expected.
Step 12: To the solution from step 11, gradually add 0.350g of Sodium- Carboxymethylcellulose 7HF (available from Aqualon). Mix until the polymer is dissolved.
Step 13: To the suspension from step 13, gradually add 1.0 lg of Polyethylene oxide of 300kDa mean molecular weight while mixing and continue to mix for not less than 60 minutes before proceeding. Step 14: Gradually add the solution from step 10 to the suspension from step 13 while mixing.
Step 15: To the reagent from step 14, add 34.2mg of Triton X-100 (available from Roche Diagnostics) and continue mixing.
Step 16: To the reagent from step 15, add the enzyme solution from step 8. Mix for no less than 30 minutes. At this point the reagent is complete. At room teperature the wet reagent mass is considered acceptable for use for 24 hours.
The measurement results illustrated in FIG. 18 show the correlation coefficient r2 between the DC current response and the glucose level as the Read Time varies for three combinations of temperature and hematocrit. These results demonstrate that a robust DC response should be anticipated for tests as fast as 1 second. However, those skilled in the art will recognise that there are undesirable variations in the sensor accuracy (correlation) due to the interfering effects of temperature and hematocrit levels, suggesting that the combined AC and DC measurement method of the present invention should produce more closely correlated results. Based upon the encouraging results obtained in Figure 18, a further test was designed using the excitation signal of Figure 19 applied to the test strip 1700. The excitation comprised a 10 kHz AC signal applied for approximately 1.8 seconds, a 20 kHz AC signal applied for approximately 0.2 seconds, a 2 Hz AC signal applied for approximately 0.2 seconds, a 1Hz AC signal applied for approximately 0.2 seconds, and a DC signal applied for approximately 0.5 seconds. The AC signals had an amplitude of 12.7 mV peak, while the DC signal had an amplitude of 550 mV. The Total Test Time was 3.0 seconds.
A covariance study using spiked venous blood samples representing five glucose levels (40, 120, 200, 400 and 600), five hematocrit levels (20, 30, 45, 60 and 70%) and five temperatures (12, 18, 24, 32 and 44 °C) was designed, resulting in 125 separate combinations. As in the previous examples, the relationship between admittance, temperature and hematocrit was examined and plotted (Figure 20 shows the admittance at 20 kHz versus hematocrit as temperature varies) and it was confirmed that the admittance was linearly related to hematocrit in a temperature dependent manner. An additional discovery, however, was that the phase angle of the AC response was correlated with hematocrit in a temperature independent manner. The phase angle of the 20 kHz AC response is plotted versus hematocrit in Figure 21. The results for phase angle measured at 10 kHz are similar. The hematocrit of the blood sample may therefore be reliably estimated using only the phase angle information as follows:
Hsst = Co + Cι(Φ10kHz - 20 Hz) + c22kHz - ikHz) (Equation 11)
For the test strip used in this Example 5, the correlation between phase angle and hematocrit was better at higher frequencies. Because of this, the c2 constant approaches zero and Hest can reliably be estimated using only the 10 kHz and 20 kHz data. Use of lower frequencies, however, allows for slight improvements in the strip-to-strip variability of the HeSt function. The present invention therefore may be used to estimate hematocrit using only AC phase angle measurements preferably made at at least one AC frequency, more preferably made at at least two AC frequencies, and most preferably made at at least four AC frequencies.
Because the hematocrit can be determined using only the AC response data, and we know from Figure 20 that admittance is linearly related to hematocrit and temperature, we can now determine the temperature of the sample under analysis using only the AC response as follows:
Test = bo + bι(YιokHz - Y20 Hz) + b2(Y2kHz - YikHz) + b3HeSt (Equation 12)
where bo, b1 ; b2 and b3 are constants. It will be appreciated that the estimation of hematocrit and temperature from the AC response data may be made with more or fewer frequency measurements, and at different frequencies than those chosen for this example. The particular frequencies that produce the most robust results will be determined by test strip geometries and dimensions. The present invention therefore may be used to estimate test sample temperature using only AC response measurements preferably made at at least one AC frequency, more preferably made at at least two AC frequencies, and most preferably made at at least four AC frequencies. Those skilled in the art will recognise that the direct measurement of the temperature of the sample under test (by means of the AC response) is a great improvement over prior art methods for estimating the temperature of the sample. Typically, a thermistor is placed in the test meter near where the test strip is inserted into the meter. Because the thermistor is measuring a temperature remote from the actual sample, it is at best only a rough approximation of the true sample temperature. Furthermore, if the sample temperature is changing (for example due to evaporation), then the thermal inertia of the test meter and even the thermistor itself will prevent the meter-mounted thermistor from accurately reflecting the true temperature of the sample under test. By contrast, the temperature estimation of the present invention is derived from measurements made within the sample under test (i.e. within the reaction zone in which the sample under test reacts with the reagent), thereby eliminating any error introduced by the sample being remote from the measuring location. Additionally, the temperature estimation of the present invention is made using data that was collected very close in time to the glucose measurement data that will be corrected using the temperature estimation, thereby further improving accuracy. This represents a significant improvement over the prior art methods.
As a demonstration of the effectiveness of the method of this Example 5 for correcting for the effects of interferants on the blood glucose measurement, the uncompensated DC current response versus known glucose concentration is plotted in Figure 22 for all 125 combinations of glucose, temperature and hematocrit (the AC measurements were ignored when plotting this data). As will be appreciated by those skilled in the art, the data exhibits huge variation with respect to hematocrit and temperature. As previously discussed, the accuracy of the DC glucose response can be greatly improved by combining the estimated hematocrit, temperature and DC response to correct for the hematocrit and temperature interference in the DC response as follows:
PRED = (ao + hctiHest + hct2HeSt2 + autest + tau2 Test) (Equation 13) + (aιDC)(l + hct3HeSt + hct4HeSt 2)(l + tau3Test + tau Test)
The constants in Equation 13 can be determined using regression analysis, as is known in the art. The present invention therefore allows one to estimate hematocrit by using the AC phase angle response (Equation 11). The estimated hematocrit and the measured AC admittance can be used to determine the estimated temperature (Equation 12). Finally, the estimated hematocrit and estimated temperature can be used with the measured DC response to obtain the predicted glucose concentration (Equation 13).
Applying the above methodology to the test data plotted in Figure 22, we obtain the predicted glucose versus DC current response illustrated in Figure 23. This data represents 125 covariant samples having hematocrit levels ranging from 20%- 70% and temperatures ranging from 12°C - 44°C. Even with these wide variations in interferant levels, the measurement method of the present invention produced an overall r2 correlation of 0.9874 using a 3.0 second Total Test Time.
Example 6: Simultaneous AC and DC Measurement Using a 0.397 μl Sample
Using the same test strip 1700 and reagent described above for Example 5, the excitation profile illustrated in Figure 24 was utilized in order to decrease the Total Test Time. As described above with respect to Example 5, it was determined that the phase angle at 20 kHz and at 10 kHz were most closely correlated with the hematocrit estimation. It was therefore decided to limit the AC portion of the excitation to these two frequencies in Example 6 in order to decrease the Total Test Time. In order to make further reductions in Total Test Time, the 10 kHz AC excitation was applied simultaneously with the DC signal (i.e. an AC signal with a DC offset), the theory being that this combined mode would allow for the collection of simultaneous results for DC current, AC phase and AC admittance, providing the fastest possible results. Therefore, the 20 kHz signal was applied for 0.9 seconds. Thereafter, the 10 kHz and DC signals were applied simultaneously for 1.0 second after a 0.1 second interval.
For this Example 6, 49 spiked venous blood samples representing seven glucose levels and seven hematocrit levels were tested. The correlation coefficient r between the DC current and the blood hematocrit was then examined at three DC measurement times: 1.1 seconds, 1.5 seconds and 1.9 seconds after sample application. These correlations are plotted versus hematocrit level in Figure 25. All of these results are comparable, although the correlation is generally poorest at 1.1 seconds and generally best at 1.5 seconds. The minimum correlation coefficient, however, exceeds 0.99.
Figure 26 illustrates the phase angle at 20 kHz plotted against hematocrit levels. The correlation between these two sets of data is very good, therefore it was decided that the 10 kHz data was unnecessary for estimating hematocrit. The hematocrit can therefore be estimated solely from the 20 kHz phase angle data as follows:
HeSt = Co + CιΦ20kHz (Equation 14)
Figure 27 illustrates the DC current response versus glucose level for all measured hematocrit levels as the read time is varied between 1.1 seconds, 1.5 seconds and 1.9 seconds. Not suφrisingly, the DC current at 1.1 seconds is greater than the DC current at 1.5 seconds, which is greater than the DC current at 1.9 seconds. Those skilled in the art will recognise that the hematocrit level has a large effect on the DC current, particularly at high glucose concentrations.
As discussed hereinabove, the accuracy of the DC glucose response can be greatly improved by compensating for the interference caused by hematocrit as follows:
PRED = (ao + hctiHest + hct2HeSt 2) + (aιDC)(l + hct3HeSt + hct HeSt 2) (Equation 15) Note that Equation 15 does not include temperature compensation terms since temperature variation was not included in the experiment of this Example 6, it can be reasonably inferred from previous examples that a Test term could be included using the 10 kHz and 20 kHz admittance values in combination with the HeSt term. Because the hematocrit can be reliably estimated using only the 20 kHz phase angle measurement data, the hematocrit compensated predicted glucose response can be determined using only this phase angle information and the measured DC response. The compensated DC response versus glucose level for only the DC read at 1.1 seconds (representing a 1.1 second Total Test Time) is illustrated in Figure 28. The data shows an overall r2 correlation of 0.9947 with a 1.1 second Total Test Time.
The same data for the 1.5 second DC read is illustrated in Figure 29, showing an overall r correlation of 0.9932 for a 1.5 second Total Test Time. The same data for the 1.9 second DC read is illustrated in Figure 30, showing an overall r2 correlation of 0.9922 for a 1.9 second Total Test Time. Suφrisingly, the r2 correlation actually decreased slightly with the longer test times. Notwithstanding this, the correlation coefficients for all three compensated data sets - where all 7 hematocrits ranging from 20% through 60% are combined - were in excess of 0.99, demonstrating the applicability of the present invention to yield a blood glucose test as fast as 1.1 seconds, combined with improved accuracy, where the sensor requires less than 0.4 microliters of blood in order to perform the glucose measurement test.
Example 7: Use of AC Phase Angle to Detect an Abused Sensor
In order to provide an extra measure of quality control to the analyte measurement process, particularly when the test system is to be used by a non- professional end user, it is desirable to detect sensors (test strips) that have been mis-dosed (double dosed, etc.), that have been previously used, or that have degraded enzymes (from being stored in too humid an environment, being too old, etc.). These conditions are collectively referred to as "abused sensors." It is desired to devise a test that will abort the analyte measurement process (or at least warn the user that the test results may not be accurate) if an abused sensor is inserted into the test meter.
When performing a blood glucose analysis, the test meter will typically make several successive current measurements as the blood sample continues to react with the reagent chemistry. As is well known in the art, this response current is known as the Cottrell current and it follows a pattern of decay as the reaction progresses. We may define a Cottrell Failsafe Ratio (CFR) as follows: The Cottrell response of the biosensor in the Confidence system can be given by:
Icoltrell (Equation 16)
Figure imgf000043_0001
where: n = electrons freed per glucose molecule
F = Faraday's Constant A = Working electrode surface area t = elapsed time since application of excitation
D = diffusion coefficient C = glucose concentration α = a cofactor-dependent constant.
All of the parameters of this equation will normally be constant for the sensor except the glucose concentration and time. We can therefore define a normalized Cottrell failsafe ratio(NCFR) as:
NCFR = = Constant (Equation 17)
Figure imgf000043_0002
As the time terms in this equation are known and constant for a sensor measurement, the ratio always yields a constant for Cottrell curves with identical sample times and intervals. Therefore, the sum of sensor currents divided by the last sensor current should yield a constant independent of glucose concentration. This relationship is used in the preferred embodiment to detect potentially faulty biosensor responses.
A Current Sum Failsafe can be devised that places a check on the Cottrell response of the sensor by summing all of the acquired currents during sensor measurement. When the final current is acquired, it is multiplied by two constants (which may be loaded into the meter at the time of manufacture or, more preferably, supplied to the meter with each lot of sensors, such as by a separate code key or by information coded onto the sensor itself). These constants represent the upper and lower threshold for allowable NCFR values.
The two products of the constants multiplied by the final current are compared to the sum of the biosensor currents. The sum of the currents should fall between the two products, thereby indicating that the ratio above was fulfilled, plus or minus a tolerance. Therefore, the preferred embodiment performs the following check when there is a single DC block: m
(I (C,) < ∑Ik < (I (CU ) (Equation 18) k=l
where Cu = upper constant from the Code Key C\ = lower constant from the Code Key
Im = final biosensor current
Because some embodiments may contain two DC blocks in the measurement sequence, a Modified Cottrell Failsafe Ratio (MCFR) can be formulated as:
T. ,-,, w.NCFR. + w2NCFR2 _ , _.
MCFR = — ! * 2 1 (Equation 19) , + w2
where wι, w2 = weighting constants (e.g. from the Code Key) NCFRj , NCFR2 = the Normalized Cottrell Failsafe Ratios for
DC blocks 1 and 2 respectively.
Therefore, the preferred embodiment performs the following check when there are two DC blocks:
(w + w2)ImiIm Ch ≤ (wxIm∑Ik + w2I ∑Ik) ≤ (wx + w2)IIm Cu (Equation 20) k=l k=\
where C = upper constant from the Code Key CL = lower constant from the Code Key Iml, I^ = final biosensor current in DC blocks 1 and 2
The NCFR (and MCFR) is correlated with hematocrit. As demonstrated hereinabove in Example 3, the AC phase angle is also correlated with hematocrit. It follows then, that the AC phase angle and the NCFR are correlated with one another. This relationship holds only if the sensor is unabused. The correlation degrades for an abused sensor.
It is therefore possible to design an equation to analyze the measured phase angle data to produce a failsafe calculation that will indicate if an abused sensor is being used. In the preferred embodiment, it was chosen to use the difference between the phase angles measured at two separate frequencies in order to make the test more robust to errors caused by parasitic resistance, etc. Applying the arctangent function to drive the two populations to different asymptotes yields the following failsafe equation:
FAILSAFE = 1000 x arctan[NCFR/(fs0 + fsι(Φ10kHz - 20kHz))] (Equation
21)
where 1000 = scaling factor
NCFR = Cottrell Failsafe Ratio fso = linear regression intercept fsi = linear regression slope ΦiokHz = phase angle at 10 kHz 20kHz = phase angle at 20 kHz
Using Equation 21, the intercept term fs0 can be chosen such that a
FAILSAFE value below zero indicates an abused sensor, while a FAILSAFE value above zero indicates a non-abused sensor. Those skilled in the art will recognise that the opposite result could be obtained by choosing a different intercept.
Use of Dose Sufficiency Electrodes
As described hereinabove, it has been recognised that accurate sample measurement requires adequate coverage of the measurement electrodes by the sample. Various methods have been used to detect the insufficiency of the sample volume in the prior art. For example, the Accu-Chek® Advantage® glucose test meter sold by Roche Diagnostics Coφoration of Indianapolis, Indiana warned the user of the possible inadequacy of the sample volume if non-Cotrellian current decay was detected by the single pair of measurement electrodes. Users were prompted to re-dose the test strip within a specified time allotment. The possibility of insufficient sample size has been heightened in recent years due to the use of capillary fill devices used in conjunction with blood lancing devices designed to minimize pain through the requirement of only extremely small sample volumes. If an inadequate amount of sample is drawn into the capillary fill space, then there is a possibility that the measurement electrodes will not be adequately covered and the measurement accuracy will be compromised. In order to overcome the problems associated with insufficient samples, various prior art solutions have been proposed, such as placing an additional electrode downstream from the measurement electrodes; or a single counter electrode having a sub-element downstream and major element upstream of a working electrode; or an indicator electrode arranged both upstream and downstream from a measurement electrode (allowing one to follow the flow progression of the sample across the working and counter electrodes or the arrival of the sample at a distance downstream). The problem associated with each of these solutions is that they each incoφorate one or the other electrode of the measurement pair in communication with either the upstream or the downstream indicator electrodes to assess the presence of a sufficient volume of sample to avoid biased test results. Despite these prior art design solutions, failure modes persist wherein the devices remain prone to misinteφretation of sample sufficiency. The present inventors have determined that such erroneous conclusions are related primarily to the distances between a downstream member of a measurement electrode pair (co- planar or opposing geometries) and the dose detection electrode, in combination with the diversity of non-uniform flow fronts. A sample traversing the capillary fill space having an aberrant (uneven) flow front can close the circuit between a measurement electrode and an indicator electrode and erroneously advise the system that sufficient sample is present to avoid a biased measurement result.
Many factors employed in the composition and/or fabrication of the test strip capillary fill spaces influence such irregular flow front behavior. These factors include:
• disparities between surface energies of different walls forming the capillary fill space. • contamination of materials or finished goods in the test strip manufacturing facility.
• unintentional introduction of a contaminant from a single component making up the walls of the capillary fill space (an example being a release agent (typically silicon) that is common to manufacturing processes wherein release liners are used).
• hydrophobic properties of adhesives (or contaminated adhesives) used in the lamination processes.
• disparate surface roughnesses on the walls of the capillary fill space.
• dimensional aspect ratios. • contaminated mesh materials within the capillary fill space. • non-homogeneous application of surfactants onto mesh materials within the capillary fill space.
Another problem with prior art dose sufficiency methodologies determined by the present inventors relates to the use of one or the other of the available measurement electrodes in electrical communication with an upstream or downstream dose detection electrode. In such arrangements, the stoichiometry of the measurement zone (the area above or between the measurement electrodes) is perturbed during the dose detect/dose sufficiency test cycle prior to making a measurement of the analyte of interest residing in the measurement zone. As sample matrices vary radically in make-up, the fill properties of these samples also vary, resulting in timing differences between sample types. Such erratic timing routines act as an additional source of imprecision and expanded total system error metrics. Trying to solve one or more of these obstacles typically can lead to 1) more complex manufacturing processes (additional process steps each bringing an additional propensity for contamination); 2) additional raw material quality control procedures; 3) more costly raw materials such as laminate composites having mixtures of hydrophobic and hydrophyllic resins and negatively impacting manufacturing costs; and 4) labor-intensive surfactant coatings of meshes and or capillary walls.
Example 8: Determination of Fluid Flow Front Behavior in a Capillary Fill Space
In order to design an electrode system that will adequately indicate dose sufficiency in a test strip employing a capillary fill space, an experiment was performed to examine the flow front shape at the leading edge of the sample as it progresses through the capillary fill space. Test fixtures comprising two sheets of clear polycarbonate sheets joined together with double-sided adhesive tape were used, where the capillary fill space was formed by cutting a channel in the double- sided tape. Use of the polycarbonate upper and lower sheets allowed the flow fronts of the sample to be videotaped as it flowed through the capillary fill space. Specifically, the test devices were laminated using laser cut 1mm thick Lexan® polycarbonate sheets (obtained from Cadillac Plastics Ltd., Westlea, Swindon SN5 7EX, United Kingdom). The top and bottom polycarbonate sheets were coupled together using double-sided adhesive tapes (#200MP High
Performance acrylic adhesive obtained from 3M Coφoration, St. Paul, MN). The capillary channels were defined by laser cutting the required width openings into the double-sided tape. Tape thicknesses of 0.05μm, 0.125μm, and 0.225μm were used to give the required channel heights. The dimensions of the capillary spaces of the test devices are tabulated in FIG. 31.
The top and bottom polycarbonate parts were laminated together with the laser cut adhesive tapes using a custom-built jig to ensure reproducible fabrication. For each test device, a fluid receptor region defineing the entrance to the capillary channel was formed by an opening pre-cut into the upper polycarbonate sheet and adhesive tape components. For each of the three channel heights, channel widths of 0.5mm, 1.00mm, 1.5mm, 2.00mm, 3.00mm, and 4.00mm were fabricated. The capillary channel length for all devices was 50mm. Twenty-eight (28) of each of the eighteen (18) device types were constructed. The assembled devices were plasma treated by Weidman Plastics Technology of Dortmund, Germany. The following plasma treatment conditions were used:
Processor: Microwave plasma processor 400
Microwave Power: 600W
Gas: O2 Pressure: 0.39 miilibar
Gas Flow: 150 ml/min
Time: 10 minutes
Surface Energy Pre-Treatment: <38 mN/m
Surface Energy Post-Treatment: 72 mN/m The plasma-treated devices were stored at 2 - 8°C when not in use. The devices were allowed to equilibrate to room temperature for one (1) hour minimum before use.
Each of the test devices was dosed with a fixed volume of venous blood having a hematocrit value of 45%. Flow and flow front behavior was captured on videotape for later analysis. It was determined that the relative dimensions of the capillary fill channel determined the flow front behavior. Devices to the left of the dashed line in FIG. 31 (devices A2, A4, B2, B4, B5, C2, C4, and C5) resulted in a convex flow front behavior, while devices to the right of the dashed line (devices A6, A8, Al l, B6, B8, Bll, C6, C8, and Cll) displayed a concave flow front behavior. Both the convex and concave flow front behaviors are schematically illustrated in FIG. 31. This data shows that the aspect ratio between the height and the width of the capillary fill space is a determining factor in whether the sample flow front is convex or concave.
Use of Dose Sufficiency Electrodes cont'd
The problems associated with a concave flow front in a capillary fill space are illustrated in FIGs. 32A-C. In each of the figures, the test strip includes a working electrode 3200, a reference electrode 3202, and a downstream dose sufficiency electrode 3204 that works in conjunction with one of the measurement electrodes 3200 or 3202. In addition to the measurement zone stoichiometry problems associated with the use of the dose sufficiency electrode 3204 in conjunction with one of the measurement electrodes discussed above, FIGs. 32A-C illustrate that a sample flow front exhibiting a concave shape can also cause biased measurement results. In each drawing, the direction of sample travel is shown by the arrow. In FIG. 32A, the portions of the sample adjacent to the capillary walls have reached the dose sufficiency electrode 3204, thereby electrically completing the DC circuit between this electrode and one of the measurement electrode pair that is being monitored by the test meter in order to make the dose sufficiency determination. Although the test meter will conclude that there is sufficient sample to make a measurement at this time, the sample clearly has barely reached the reference electrode 3202 and any measurement results obtained at this time will be highly biased.
Similarly, FIG. 32B illustrates the situation where the dose sufficiency electrode 3204 has been contacted (indicating that the measurement should be started), but the reference electrode 3202 is only partially covered by the sample. Although the sample has reached the reference electrode 3202 at this time, the reference electrode 3202 is not completely covered by sample, therefore any measurement results obtained at this time will be partially biased. Both of the situations illustrated in FIGs. 32A-B will therefore indicate a false positive for dose sufficiency, thereby biasing the measurement test results. Only in the situation illustrated in FIG. 32C, where the reference electrode 3202 is completely covered by the sample, will the measurement results be unbiased due to the extent of capillary fill in the measurement zone.
The present invention solves the stoichiometric problems associated with the prior art designs pairing the dose sufficiency electrode with one of the measurement electrodes when making the dose sufficiency determination. As shown in FIG. 33, the present invention comprehends a test strip having an independent pair of dose sufficiency electrodes positioned downstream from the measurement electrodes. The test strip is indicated generally as 3300, and includes a measurement electrode pair consisting of a counter electrode 3302 and a working electrode 3304. The electrodes may be formed upon any suitable substrate in a multilayer test strip configuration as is known in the art and described hereinabove. The multilayer configuration of the test strip provides for the formation of a capillary fill space 3306, also as known in the art. Within the capillary fill space 3306, and downstream (relative to the direction of sample flow) from the measurement electrodes 3302 and 3304 are formed a dose sufficiency working electrode 3308 and a dose sufficiency counter electrode 3310, together forming a dose sufficiency electrode pair.
When the test strip 3300 is inserted into the test meter, the test meter will continuously check for a conduction path between the dose sufficiency electrodes 3308 and 3310 in order to determine when the sample has migrated to this region of the capillary fill space. Once the sample has reached this level, the test meter may be programmed to conclude that the measurement electrodes are covered with sample and the sample measurement sequence may be begun. It will be appreciated that, unlike as required with prior art designs, no voltage or current need be applied to either of the measurement electrodes 3302 and 3304 during the dose sufficiency test using the test strip design of FIG. 33. Thus the stoichiometry of the measurement zone is not perturbed during the dose sufficiency test cycle prior to making a measurement of the analyte of interest residing in the measurement zone. This represents a significant improvement over the dose sufficiency test methodologies of the prior art. The test strip 3300 is also desirable for judging dose sufficiency when the capillary fill space is designed to produce samples that exhibit a convex flow front while filling the capillary fill space 3306, as illustrated in FIG. 34A. As can be seen, the measurement zone above the measurement electrodes 3302 and 3304 is covered with sample when the convex flow front reaches the dose sufficiency electrode pair 3308,3310. The test strip design 3300 may not, however, produce ideal results if the capillary fill space 3306 allows the sample to exhibit a concave flow front while filling, as shown in FIG. 34B. As can be seen, the peripheral edges of the concave flow front reach the dose sufficiency electrodes 3308,3310 before the measurement zone has been completely covered with sample. With DC or low frequency excitation (discussed in greater detail hereinbelow), the dose sufficiency electrodes 3308,3310 will indicate sample sufficiency as soon as they are both touched by the edges of the flow front. Therefore, the dose sufficiency electrode design shown in the test strip of FIG. 33 works best when the sample filling the capillary space 3306 exhibits a convex flow front. It will be appreciated that the dose sufficiency electrodes 3308,3310 have their longest axis within the capillary fill space 3306 oriented peφendicular to the longitudinal axis of the capillary fill space 3306. Such electrodes are referred to herein as "peφendicular dose sufficiency electrodes." An alternative dose sufficiency electrode arrangement is illustrated in FIGs. 35A-B. As shown in FIG. 35A, the present invention also comprehends a test strip having an independent pair of dose sufficiency electrodes positioned downstream from the measurement electrodes, where the dose sufficiency electrodes have their longest axis within the capillary fill space oriented parallel to the longitudinal axis of the capillary fill space. Such electrodes are referred to herein as "parallel dose sufficiency electrodes." The test strip in FIG. 35 is indicated generally as 3500, and includes a measurement electrode pair consisting of a counter electrode 3502 and a working electrode 3504. The electrodes may be formed upon any suitable substrate in a multilayer test strip configuration as is known in the art and described hereinabove. The multilayer configuration of the test strip provides for the formation of a capillary fill space 3506, also as known in the art. Within the capillary fill space 3506, and downstream (relative to the direction of sample flow) from the measurement electrodes 3502 and 3504 are formed a dose sufficiency working electrode 3508 and a dose sufficiency counter electrode 3510, together forming a parallel dose sufficiency electrode pair.
When the test strip 3500 is inserted into the test meter, the test meter will continuously check for a conduction path between the dose sufficiency electrodes 3508 and 3510 in order to determine when the sample has migrated to this region of the capillary fill space. Once the sample has reached this level, the test meter may be programmed to conclude that the measurement electrodes are covered with sample and the sample measurement sequence may be begun. It will be appreciated that, as with the test strip 3300 (and unlike as required with prior art designs), no voltage or current need be applied to either of the measurement electrodes 3502 and 3504 during the dose sufficiency test using the test strip design of FIG. 35. Thus the stoichiometry of the measurement zone is not perturbed during the dose sufficiency test cycle prior to making a measurement of the analyte of interest residing in the measurement zone. This represents a significant improvement over the dose sufficiency test methodologies of the prior art.
A further improved operation is realized with the parallel dose sufficiency electrodes of the test strip 3500 when the dose sufficiency electrodes are energized with a relatively high frequency AC excitation signal. When a relatively high frequency AC signal is used as the dose sufficiency excitation signal, the dose sufficiency electrodes 3508,3510 display significant edge effects, wherein the excitation signal traverses the gap between the electrodes only when the electrode edges along the gap are covered with the sample fluid. The test strip 3500 is illustrated in enlarged size in FIG. 36 (with only the electrode portions lying within the capillary fill space 3506 and the strip-to-meter electrode contact pads visible). When one of the pair of dose sufficiency electrodes 3508,3510 is excited with an AC signal, the majority of the signal travels from one electrode edge to the edge of the other electrode (when the edges are covered with sample), rather than from the upper flat surface of one electrode to the upper flat surface of the other electrode. These paths of edge-to-edge electrical communication are illustrated schematically as the electric field lines 3602 in FIG. 36.
Higher AC frequencies produce the best edge-only sensitivity from the dose sufficiency electrodes. In the preferred embodiment, a 9 mVπns (+/- 12.7 mV peak-to-peak) excitation signal of 10kHz is used to excite one of the dose sufficiency electrodes. The gap width GW between the edges of the dose sufficiency electrodes 3508,3510 is preferably 100-300 μm, more preferably 150- 260 μm, and most preferably 255 μm. A smaller gap width GW increases the amount of signal transmitted between dose sufficiency electrodes whose edges are at least partially covered by sample; however, the capacitance of the signal transmission path increases with decreasing gap width GW.
An advantage of the parallel dose sufficiency electrode design of FIGs. 35 and 36, when used with AC excitation, is that there is substantially no electrical communication between the electrodes until the sample covers at least a portion of the edges along the electrode gap. Therefore, a sample exhibiting the concave flow front of FIG. 35A, where the illustrated sample is touching both of the dose sufficiency electrodes 3508,3510 but is not touching the electrode edges along the gap, will not produce any significant electrical communication between the dose sufficiency electrodes. The test meter will therefore not form a conclusion of dose sufficiency until the sample has actually bridged the dose sufficiency electrodes between the electrode edges along the gap. This will happen only after the rearmost portion of the concave flow front has reached the dose sufficiency electrodes 3508,3510, at which point the sample has completely covered the measurement zone over the measurement electrodes. As can be seen in FIG. 35B, convex sample flow fronts will activate the dose sufficiency electrodes 3508,3510 as soon as the flow front reaches the dose sufficiency electrodes (at which point the sample has completely covered the measurement zone over the measurement electrodes). Another advantage to the parallel dose sufficiency electrodes illustrated in FIGs. 35 and 36 is that the amount of signal transmitted between the electrodes is proportional to the amount of the gap edges that is covered by the sample. By employing an appropriate threshold value in the test meter, a conclusion of dose sufficiency can therefore be withheld until the sample has covered a predetermined portion of the dose sufficiency electrode gap edge. Furthermore, an analysis of the dose sufficiency signal will allow the test meter to record the percentage of fill of the capillary fill space for each measurement made by the test meter, if desired. While the electrode geometry itself demonstrates an advantage over previous embodiments in terms of detecting an adequate sample, particularly in the case of a convex flow front, it was found that further improvement is achieved in the use of AC responses over DC responses for sample detection. DC responses have the problems of being sensitive to variations in, for example, temperature, hematocrit and the analyte (glucose for example). AC responses at sufficiently high frequency can be made robust to the variation in the analyte concentration. Further, the AC response generated at sufficiently high frequencies in such capillary fill devices is primarily limited by the amount of the parallel gap between the electrode edges which is filled by the sample. Thus, for a convex flow front, little or no AC response (in this case admittance) is perceived until the trough of the flow front actually intrudes within the parallel edges of the sample sufficiency electrodes. Further, by means of threshold calibration, the sensor can be made more or less sensitive as is deemed advantageous, with a higher threshold for admittance requiring more of the parallel gap to be filled before test initiation. A further limitation of existing devices is the inability of the electrode geometry to discern the amount of time needed to fill the capillary space of the sensor. This limitation is caused by having interdependence of the dose sufficiency electrode and the measurement electrodes. This is a further advantage of independent dose sufficiency electrodes. In the preferred embodiment a signal is first applied across the measurement electrodes prior to dosing. When a response is observed, the potential is immediately switched off and a second signal is applied across the dose sufficiency electrodes during which time the system both looks for a response to the signal (indicating electrode coverage) and marks the duration between the first event (when a response is observed at the measurement electrodes) and the second event (when a response is observed at the dose sufficiency electrodes). In cases where very long intervals may lead to erroneous results, it is possible to establish a threshold within which acceptable results may be obtained and outside of which a failsafe is triggered, preventing a response or at a minimum warning the user of potential inaccuracy. The amount of time lag between dosing and detection of a sufficient sample that is considered allowable is dependent upon the particular sensor design and chemistry. Alternatively, an independent pair of dose detection electrodes (not shown) may be added upstream from the measurement electrodes in order to detect when the sample is first applied to the sensor.
While a DC signal could be used for detection in either or both of the above events, the preferred embodiment uses an AC signal at sufficiently high frequency to avoid unnecessarily perturbing the electrochemical response at the measurement electrodes and to provide robust detection with respect to flow front irregularities.
All publications, prior applications, and other documents cited herein are hereby incoφorated by reference in their entirety as if each had been individually incoφorated by reference and fully set forth.
While the invention has been illustrated and described in detail in the drawings and foregoing description, the description is to be considered as illustrative and not restrictive in character. Only the preferred embodiment, and certain other embodiments deemed helpful in further explaining how to make or use the preferred embodiment, have been shown. All changes and modifications that come within the spirit of the invention are desired to be protected.

Claims

What is claimed is:
1. A method of performing a measurement on a biological fluid in a test strip comprising: providing a biological fluid test strip including a capillary fill chamber extending a length along the test strip from an intake opening to a terminus, a first pair of electrodes in operative communication with the chamber, and a second pair of electrodes in operative communication with the chamber; dosing the test strip with a biological fluid effective to cause the biological fluid to flow from the intake opening toward the terminus; applying a first test signal to one of the first pair of electrodes; measuring a first response to the first test signal at the other of the first pair of electrodes; maintaining the first pair of electrodes in an inoperative state upon the measuring the first response; applying a second test signal to one of the second pair of electrodes; measuring a second response to the second test signal at the other of the second pair of electrodes; and performing a measurement upon the biological fluid after the measuring the second response.
2. The method of claim 1 wherein the measuring the first response to the first test signal is effective to indicate a contact of the first pair of electrodes and the biological fluid.
3. The method of claim 1 wherein the measuring the second response to the second test signal is effective to indicate a contact of the second pair of electrodes and the biological fluid.
4. The method of claim 1 wherein the measuring the first response to the first test signal is effective to indicate a contact of the first pair of electrodes and the biological fluid and the measuring the second response to the second test signal is effective to indicate a contact of the second pair of electrodes and the biological fluid.
5. The method of claim 1 wherein the performing a measurement upon the biological fluid includes applying a measurement test signal to one of the first pair of electrodes.
6. The method of claim 1 further comprising providing a pair of measurement electrodes in operative communication with the chamber wherein the performing a measurement upon the biological fluid includes applying a measurement test signal to one of the measurement electrodes.
7. A method of indicating acceptable fill time of a biological fluid in a test strip comprising: providing a biological fluid test strip including a capillary fill chamber extending a length along the test strip from an intake opening to a terminus, a first pair of electrodes in operative communication with the chamber, and a second pair of electrodes in operative communication with the chamber; dosing the test strip with a biological fluid effective to cause the biological fluid to flow from the intake opening toward the terminus; flowing a biological fluid from the opening toward the terminus; first determining when the biological fluid contacts the first electrodes; second determining when the biological fluid contacts the second electrodes; determining a fill time value based upon the first determining and the second determining; and comparing the fill time value to a predetermined value.
8. The method of claim 7 further comprising: indicating an error condition if the fill time value exceeds the predetermined value.
9. The method of claim 7 further comprising: indicating an error condition if the fill time value is greater than or equal to the predetermined value.
10. The method of claim 7 further comprising: performing a measurement upon the biological fluid if the fill time value is less than the predetermined value.
11. The method of claim 7 further comprising: performing a measurement upon the biological fluid if the fill time value is less than or equal to the predetermined value.
PCT/US2004/019627 2003-06-20 2004-06-18 Method for analyte measurement employing maximum dosing time delay WO2004113913A1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US48029803P 2003-06-20 2003-06-20
US60/480,298 2003-06-20
US10/687,850 US7597793B2 (en) 2003-06-20 2003-10-17 System and method for analyte measurement employing maximum dosing time delay
US10/687,850 2003-10-17

Publications (1)

Publication Number Publication Date
WO2004113913A1 true WO2004113913A1 (en) 2004-12-29

Family

ID=33519464

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2004/019627 WO2004113913A1 (en) 2003-06-20 2004-06-18 Method for analyte measurement employing maximum dosing time delay

Country Status (2)

Country Link
US (1) US7597793B2 (en)
WO (1) WO2004113913A1 (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2151682A1 (en) * 2007-04-25 2010-02-10 Arkray, Inc. Substrate concentration measurement method and substrate concentration measurement apparatus
EP2511698A1 (en) * 2008-01-17 2012-10-17 LifeScan, Inc. Method of identifying an error in performing a test with a test strip
US8449740B2 (en) 2006-03-31 2013-05-28 Lifescan, Inc. Systems and methods for discriminating control solution from a physiological sample
US8551320B2 (en) 2008-06-09 2013-10-08 Lifescan, Inc. System and method for measuring an analyte in a sample
US8617381B2 (en) 2009-06-23 2013-12-31 Bayer Healthcare Llc System and apparatus for determining temperatures in a fluid analyte system
US8647489B2 (en) 2005-09-30 2014-02-11 Bayer Healthcare Llc Gated voltammetry devices
US8778168B2 (en) 2007-09-28 2014-07-15 Lifescan, Inc. Systems and methods of discriminating control solution from a physiological sample
US8877035B2 (en) 2005-07-20 2014-11-04 Bayer Healthcare Llc Gated amperometry methods
US9005527B2 (en) 2006-10-24 2015-04-14 Bayer Healthcare Llc Transient decay amperometry biosensors
US9189598B2 (en) 2007-05-30 2015-11-17 Bayer Healthcare Llc Fluid analyte meter
US9410917B2 (en) 2004-02-06 2016-08-09 Ascensia Diabetes Care Holdings Ag Method of using a biosensor
US9933385B2 (en) 2007-12-10 2018-04-03 Ascensia Diabetes Care Holdings Ag Method of using an electrochemical test sensor
RU2690065C2 (en) * 2014-10-27 2019-05-30 Цилаг Гмбх Интернэшнл Diffusion determining method

Families Citing this family (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7955559B2 (en) 2005-11-15 2011-06-07 Nanomix, Inc. Nanoelectronic electrochemical test device
US7004928B2 (en) 2002-02-08 2006-02-28 Rosedale Medical, Inc. Autonomous, ambulatory analyte monitor or drug delivery device
US7312095B1 (en) * 2002-03-15 2007-12-25 Nanomix, Inc. Modification of selectivity for sensing for nanostructure sensing device arrays
US7052652B2 (en) 2003-03-24 2006-05-30 Rosedale Medical, Inc. Analyte concentration detection devices and methods
US9234867B2 (en) 2003-05-16 2016-01-12 Nanomix, Inc. Electrochemical nanosensors for biomolecule detection
US8425745B2 (en) * 2006-10-06 2013-04-23 Nanomix, Inc. Electrochemical nanosensors for biomolecule detection
US8148164B2 (en) 2003-06-20 2012-04-03 Roche Diagnostics Operations, Inc. System and method for determining the concentration of an analyte in a sample fluid
US20070264721A1 (en) * 2003-10-17 2007-11-15 Buck Harvey B System and method for analyte measurement using a nonlinear sample response
US7645374B2 (en) * 2005-04-15 2010-01-12 Agamatrix, Inc. Method for determination of analyte concentrations and related apparatus
US20060281187A1 (en) 2005-06-13 2006-12-14 Rosedale Medical, Inc. Analyte detection devices and methods with hematocrit/volume correction and feedback control
GB0514728D0 (en) * 2005-07-19 2005-08-24 Hypoguard Ltd Biosensor and method of manufacture
US20070017824A1 (en) * 2005-07-19 2007-01-25 Rippeth John J Biosensor and method of manufacture
CA2623589C (en) 2005-09-30 2014-07-22 Intuity Medical, Inc. Catalysts for body fluid sample extraction
US8801631B2 (en) 2005-09-30 2014-08-12 Intuity Medical, Inc. Devices and methods for facilitating fluid transport
WO2007058999A1 (en) * 2005-11-14 2007-05-24 Bayer Healthcare Llc Test sensor reagent having cellulose polymers
US8398443B2 (en) * 2006-04-21 2013-03-19 Roche Diagnostics Operations, Inc. Biological testing system and connector therefor
WO2007131036A1 (en) * 2006-05-03 2007-11-15 Bayer Healthcare Llc Underfill detection system for an electrochemical biosensor
US7966859B2 (en) * 2006-05-03 2011-06-28 Bayer Healthcare Llc Underfill detection system for a biosensor
US8177957B2 (en) * 2006-08-22 2012-05-15 Lawrence Livermore National Security, Llc Multiple frequency method for operating electrochemical sensors
US8080153B2 (en) 2007-05-31 2011-12-20 Abbott Diabetes Care Inc. Analyte determination methods and devices
EP2174129A1 (en) 2007-08-06 2010-04-14 Bayer Healthcare, LLC System and method for automatic calibration
US8241488B2 (en) * 2007-11-06 2012-08-14 Bayer Healthcare Llc Auto-calibrating test sensors
US7809512B2 (en) * 2007-11-11 2010-10-05 Bayer Healthcare Llc Biosensor coding system
USD612279S1 (en) 2008-01-18 2010-03-23 Lifescan Scotland Limited User interface in an analyte meter
IL197532A0 (en) 2008-03-21 2009-12-24 Lifescan Scotland Ltd Analyte testing method and system
WO2009145920A1 (en) 2008-05-30 2009-12-03 Intuity Medical, Inc. Body fluid sampling device -- sampling site interface
JP5642066B2 (en) * 2008-06-06 2014-12-17 インテュイティ メディカル インコーポレイテッド Method and apparatus for performing an assay to determine the presence or concentration of an analyte contained in a sample of body fluid
ES2907152T3 (en) 2008-06-06 2022-04-22 Intuity Medical Inc Blood glucose meter and method of operation
USD611151S1 (en) 2008-06-10 2010-03-02 Lifescan Scotland, Ltd. Test meter
USD611372S1 (en) 2008-09-19 2010-03-09 Lifescan Scotland Limited Analyte test meter
BRPI0913784A2 (en) * 2008-09-30 2015-10-20 Menai Medical Technologies Ltd "sample measurement system, sampling plate, measuring device, adapter, data charger, sampling plate production method, continuous sheet production method, continuous sheet, apparatus, method for testing a medical condition, and , diagnostic kit to test a medical condition "
CA2739091A1 (en) * 2008-10-03 2010-04-08 Bayer Healthcare Llc System and method for predicting ambient temperature in a fluid analyte meter
US8424763B2 (en) 2008-10-07 2013-04-23 Bayer Healthcare Llc Method of forming an auto-calibration circuit or label
KR101003077B1 (en) * 2008-10-16 2010-12-21 세종공업 주식회사 Electrochemical biosensor structure and measuring method using the same
EP2506768B1 (en) 2009-11-30 2016-07-06 Intuity Medical, Inc. Calibration material delivery devices and methods
TWI440853B (en) * 2009-12-14 2014-06-11 Taidoc Technology Corp Electrochemical biosensing test strip, biosensing meter, system and measuring method for analyte measurement incorporating a hematocrit correction
US8877034B2 (en) * 2009-12-30 2014-11-04 Lifescan, Inc. Systems, devices, and methods for measuring whole blood hematocrit based on initial fill velocity
US8101065B2 (en) 2009-12-30 2012-01-24 Lifescan, Inc. Systems, devices, and methods for improving accuracy of biosensors using fill time
GB201005359D0 (en) 2010-03-30 2010-05-12 Menai Medical Technologies Ltd Sampling plate
GB201005357D0 (en) 2010-03-30 2010-05-12 Menai Medical Technologies Ltd Sampling plate
EP2584964B1 (en) 2010-06-25 2021-08-04 Intuity Medical, Inc. Analyte monitoring devices
CN103003440B (en) 2010-07-23 2015-11-25 霍夫曼-拉罗奇有限公司 Containing the composition of zwitterionic buffer and the purposes in electroanalysis apparatus and method thereof
US8603323B2 (en) * 2010-09-20 2013-12-10 Lifescan, Inc. Apparatus and process for improved measurements of a monitoring device
US8932445B2 (en) 2010-09-30 2015-01-13 Cilag Gmbh International Systems and methods for improved stability of electrochemical sensors
US8617370B2 (en) 2010-09-30 2013-12-31 Cilag Gmbh International Systems and methods of discriminating between a control sample and a test fluid using capacitance
US9213015B2 (en) 2011-02-23 2015-12-15 Panasonic Healthcare Holdings Co., Ltd. Biological sample measuring device
EP4339613A2 (en) 2011-08-03 2024-03-20 Intuity Medical, Inc. Body fluid sampling arrangement
US9903830B2 (en) 2011-12-29 2018-02-27 Lifescan Scotland Limited Accurate analyte measurements for electrochemical test strip based on sensed physical characteristic(s) of the sample containing the analyte
JP6356705B2 (en) 2013-03-15 2018-07-11 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Scaling data method and device, apparatus and system using biosensor algorithm for construction
EP3388824B1 (en) 2013-03-15 2021-04-14 Roche Diabetes Care GmbH Methods of detecting high antioxidant levels during electrochemical measurements and failsafing an analyte concentration therefrom as well as devices and systems incorporting the same
EP2972273B1 (en) 2013-03-15 2020-10-21 Roche Diabetes Care GmbH Methods of using information from recovery pulses in electrochemical analyte measurements as well as devices incorporating the same
EP2972268B1 (en) 2013-03-15 2017-05-24 Roche Diabetes Care GmbH Methods of failsafing electrochemical measurements of an analyte as well as devices, apparatuses and systems incorporating the same
JP2016522070A (en) 2013-06-21 2016-07-28 インテュイティ メディカル インコーポレイテッド Analyte monitoring system using audible feedback
US9243276B2 (en) 2013-08-29 2016-01-26 Lifescan Scotland Limited Method and system to determine hematocrit-insensitive glucose values in a fluid sample
US9459231B2 (en) 2013-08-29 2016-10-04 Lifescan Scotland Limited Method and system to determine erroneous measurement signals during a test measurement sequence
GB201321430D0 (en) 2013-12-04 2014-01-15 Spd Swiss Prec Diagnostics Gmbh Assay device
KR101666978B1 (en) 2014-09-17 2016-10-24 주식회사 아이센스 Apparatus and Method for measuring concentration of Whole Blood Samples Using the same
KR102007585B1 (en) * 2014-11-03 2019-08-05 에프. 호프만-라 로슈 아게 Electrode arrangements for electrochemical test elements and methods of use thereof
US20160178561A1 (en) * 2014-12-17 2016-06-23 Lifescan Scotland Limited Hand-held test meter with test strip electrode to ground-reference switch circuit block
KR102372113B1 (en) 2016-10-05 2022-03-07 에프. 호프만-라 로슈 아게 Detection reagents and electrode arrangements for multi-analyte diagnostic test elements, and methods of using the same
EP3618699A4 (en) * 2017-05-05 2021-02-24 Trividia Health, Inc. Methods and systems for hematocrit measurement
CN111189883A (en) * 2020-01-17 2020-05-22 杭州瑞盟科技有限公司 Blood sugar detection system and method

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0537761A2 (en) * 1991-10-18 1993-04-21 Matsushita Electric Industrial Co., Ltd. A biosensor and a method for measuring a concentration of a substrate in a sample
DE19936693A1 (en) * 1999-08-04 2001-02-08 Lre Technology Partner Gmbh Instrument for the measurement of blood sugar concentrations has a test field with electrodes for the test strip and a circuit for measurement/evaluation of the current strength for display
US20020175075A1 (en) * 2001-05-21 2002-11-28 Yingping Deng Electrochemical sensor
EP1275732A1 (en) * 2001-06-11 2003-01-15 Bayer Corporation Electrochemical test sensor with an underfill detection system
WO2003091717A1 (en) * 2002-04-25 2003-11-06 Home Diagnostics, Inc. Systems and methods for blood glucose sensing

Family Cites Families (174)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3526480A (en) 1966-12-15 1970-09-01 Xerox Corp Automated chemical analyzer
US3551295A (en) 1967-11-29 1970-12-29 Northrop Corp Microbiological detection and identification system
US3621381A (en) 1968-10-16 1971-11-16 Leeds & Northrup Co Coulometric system having compensation for temperature induced viscosity changes
BE754658A (en) * 1969-08-12 1971-02-10 Merck Patent Gmbh INDICATOR SHEET, CONSISTING OF AN IMPREGNATED, ABSORBENT, SHEATHED HAIR MATERIAL
US3661748A (en) 1970-04-07 1972-05-09 Instrumentation Labor Inc Fault sensing instrumentation
US3770607A (en) 1970-04-07 1973-11-06 Secretary Glucose determination apparatus
US3919627A (en) 1970-08-06 1975-11-11 Gerald F Allen Conductivity measuring method and apparatus utilizing coaxial electrode cells
US3776832A (en) 1970-11-10 1973-12-04 Energetics Science Electrochemical detection cell
US3720093A (en) * 1970-12-03 1973-03-13 Us Navy Carbon dioxide indicating meter
CH559912A5 (en) 1971-09-09 1975-03-14 Hoffmann La Roche
US3763422A (en) 1971-10-21 1973-10-02 Corning Glass Works Method and apparatus for electrochemical analysis of small samples of blood
US3925183A (en) 1972-06-16 1975-12-09 Energetics Science Gas detecting and quantitative measuring device
US3902970A (en) 1973-07-30 1975-09-02 Leeds & Northrup Co Flow-through amperometric measuring system and method
CH585907A5 (en) * 1973-08-06 1977-03-15 Hoffmann La Roche
US3937615A (en) * 1974-12-17 1976-02-10 Leeds & Northrup Company Auto-ranging glucose measuring system
FR2295419A1 (en) 1974-12-21 1976-07-16 Kyoto Daiichi Kagaku Kk REFLECTANCE MEASURING DEVICE AND COMPOSITE TEST PAPER STRUCTURE SUBJECT TO SUCH MEASUREMENT
US4052596A (en) 1974-12-23 1977-10-04 Hycel, Inc. Automatic hematology analyzer
US4008448A (en) * 1975-10-03 1977-02-15 Polaroid Corporation Solenoid with selectively arrestible plunger movement
US4230537A (en) 1975-12-18 1980-10-28 Monsanto Company Discrete biochemical electrode system
US4040908A (en) 1976-03-12 1977-08-09 Children's Hospital Medical Center Polarographic analysis of cholesterol and other macromolecular substances
US4065263A (en) 1976-04-02 1977-12-27 Woodbridge Iii Richard G Analytical test strip apparatus
US4053381A (en) 1976-05-19 1977-10-11 Eastman Kodak Company Device for determining ionic activity of components of liquid drops
US4123701A (en) 1976-07-01 1978-10-31 United States Surgical Corporation Disposable sample card having a well with electrodes for testing a liquid sample
US4127448A (en) 1977-02-28 1978-11-28 Schick Karl G Amperometric-non-enzymatic method of determining sugars and other polyhydroxy compounds
JPS5912135B2 (en) 1977-09-28 1984-03-21 松下電器産業株式会社 enzyme electrode
JPS5460996A (en) 1977-10-22 1979-05-16 Mitsubishi Chem Ind Method of measuring amount of sugar
US4214968A (en) 1978-04-05 1980-07-29 Eastman Kodak Company Ion-selective electrode
DE2817363C2 (en) 1978-04-20 1984-01-26 Siemens AG, 1000 Berlin und 8000 München Method for determining the concentration of sugar and a suitable electrocatalytic sugar sensor
DE2823485C2 (en) 1978-05-30 1986-03-27 Albert Prof. Dr. 3550 Marburg Huch Trough electrode
US4184936A (en) * 1978-07-24 1980-01-22 Eastman Kodak Company Device for determining ionic activity
US4233029A (en) 1978-10-25 1980-11-11 Eastman Kodak Company Liquid transport device and method
US4225410A (en) 1978-12-04 1980-09-30 Technicon Instruments Corporation Integrated array of electrochemical sensors
US4329642A (en) 1979-03-09 1982-05-11 Siliconix, Incorporated Carrier and test socket for leadless integrated circuit
US4273134A (en) 1979-05-22 1981-06-16 Biochem International Inc. Fixation ring assembly and method of assembling a sensor head
US4273639A (en) 1979-06-20 1981-06-16 Eastman Kodak Company Capillary bridge in apparatus for determining ionic activity
US4297569A (en) 1979-06-28 1981-10-27 Datakey, Inc. Microelectronic memory key with receptacle and systems therefor
US4265250A (en) 1979-07-23 1981-05-05 Battle Research And Development Associates Electrode
US4263343A (en) 1979-08-13 1981-04-21 Eastman Kodak Company Reference elements for ion-selective membrane electrodes
US4301412A (en) 1979-10-29 1981-11-17 United States Surgical Corporation Liquid conductivity measuring system and sample cards therefor
US4303887A (en) 1979-10-29 1981-12-01 United States Surgical Corporation Electrical liquid conductivity measuring system
US4628193A (en) 1980-01-30 1986-12-09 Blum Alvin S Code reading operations supervisor
US4323536A (en) 1980-02-06 1982-04-06 Eastman Kodak Company Multi-analyte test device
US4413407A (en) 1980-03-10 1983-11-08 Eastman Kodak Company Method for forming an electrode-containing device with capillary transport between electrodes
US4816224A (en) * 1980-08-05 1989-03-28 Boehringer Mannheim Gmbh Device for separating plasma or serum from whole blood and analyzing the same
DE3029579C2 (en) 1980-08-05 1985-12-12 Boehringer Mannheim Gmbh, 6800 Mannheim Method and means for separating plasma or serum from whole blood
US4407959A (en) 1980-10-29 1983-10-04 Fuji Electric Co., Ltd. Blood sugar analyzing apparatus
US4413628A (en) 1980-11-19 1983-11-08 Tamulis Walter G pH Monitor electrode electrolyte cartridge
US4420564A (en) 1980-11-21 1983-12-13 Fuji Electric Company, Ltd. Blood sugar analyzer having fixed enzyme membrane sensor
DE3047782A1 (en) * 1980-12-18 1982-07-08 Drägerwerk AG, 2400 Lübeck CIRCUIT FOR THE CORRECTION OF THE SENSOR OUTPUT SIZE
US4436094A (en) * 1981-03-09 1984-03-13 Evreka, Inc. Monitor for continuous in vivo measurement of glucose concentration
US4407290A (en) 1981-04-01 1983-10-04 Biox Technology, Inc. Blood constituent measuring device and method
AT369254B (en) 1981-05-07 1982-12-27 Otto Dipl Ing Dr Tech Prohaska MEDICAL PROBE
US4440175A (en) 1981-08-10 1984-04-03 University Patents, Inc. Membrane electrode for non-ionic species
DE3133826A1 (en) 1981-08-27 1983-03-10 Boehringer Mannheim Gmbh, 6800 Mannheim ANALYSIS TEST STRIP AND METHOD FOR THE PRODUCTION THEREOF
DE3137174A1 (en) 1981-09-18 1983-04-07 Boehringer Mannheim Gmbh, 6800 Mannheim DEVICE FOR THE OPTICAL DETECTION OF A CODING ON A DIAGNOSTIC TEST STRIP
DE3278334D1 (en) 1981-10-23 1988-05-19 Genetics Int Inc Sensor for components of a liquid mixture
US4431004A (en) * 1981-10-27 1984-02-14 Bessman Samuel P Implantable glucose sensor
NZ199380A (en) * 1981-12-23 1986-08-08 J R Baker Determination of serum glucose levels in blood samples
DE3202067C2 (en) 1982-01-23 1984-06-20 Holger Dr. 5100 Aachen Kiesewetter Device for determining the hematocrit value
DE3228542A1 (en) 1982-07-30 1984-02-02 Siemens AG, 1000 Berlin und 8000 München METHOD FOR DETERMINING THE CONCENTRATION OF ELECTROCHEMICALLY IMPLEMENTABLE SUBSTANCES
DE3228551A1 (en) 1982-07-30 1984-02-02 Siemens AG, 1000 Berlin und 8000 München METHOD FOR DETERMINING SUGAR CONCENTRATION
US4571292A (en) * 1982-08-12 1986-02-18 Case Western Reserve University Apparatus for electrochemical measurements
US4679562A (en) 1983-02-16 1987-07-14 Cardiac Pacemakers, Inc. Glucose sensor
CA1219040A (en) 1983-05-05 1987-03-10 Elliot V. Plotkin Measurement of enzyme-catalysed reactions
DE3326689A1 (en) * 1983-07-23 1985-01-31 Boehringer Mannheim Gmbh, 6800 Mannheim METHOD AND DEVICE FOR PRODUCING A TEST STRIP
US4517291A (en) 1983-08-15 1985-05-14 E. I. Du Pont De Nemours And Company Biological detection process using polymer-coated electrodes
US4552458A (en) 1983-10-11 1985-11-12 Eastman Kodak Company Compact reflectometer
SE8305704D0 (en) * 1983-10-18 1983-10-18 Leo Ab Cuvette
US4703017C1 (en) 1984-02-14 2001-12-04 Becton Dickinson Co Solid phase assay with visual readout
DE3407754A1 (en) 1984-03-02 1985-09-12 Boehringer Mannheim Gmbh, 6800 Mannheim DEVICE FOR DETERMINING THE DIFFUSION REFLECTIVITY OF A SAMPLE AREA OF SMALL DIMENSIONS
US4849330A (en) 1984-04-27 1989-07-18 Molecular Devices Corporation Photoresponsive redox detection and discrimination
US4820399A (en) 1984-08-31 1989-04-11 Shimadzu Corporation Enzyme electrodes
US4648665A (en) * 1984-10-16 1987-03-10 Amp Incorporated Electronic key assemblies
US4713347A (en) 1985-01-14 1987-12-15 Sensor Diagnostics, Inc. Measurement of ligand/anti-ligand interactions using bulk conductance
GB8504521D0 (en) 1985-02-21 1985-03-27 Genetics Int Inc Electrochemical assay
US5279294A (en) * 1985-04-08 1994-01-18 Cascade Medical, Inc. Medical diagnostic system
US4652830A (en) * 1985-04-18 1987-03-24 Eg&G Ocean Products, Inc. Analyzer for comparative measurements of bulk conductivity
US4671288A (en) 1985-06-13 1987-06-09 The Regents Of The University Of California Electrochemical cell sensor for continuous short-term use in tissues and blood
DE3687646T3 (en) * 1985-06-21 2001-05-31 Matsushita Electric Ind Co Ltd BIOSENSOR AND THEIR PRODUCTION.
US4686479A (en) 1985-07-22 1987-08-11 Young Chung C Apparatus and control kit for analyzing blood sample values including hematocrit
US4806312A (en) * 1985-08-28 1989-02-21 Miles Inc. Multizone analytical element having detectable signal concentrating zone
US4806311A (en) * 1985-08-28 1989-02-21 Miles Inc. Multizone analytical element having labeled reagent concentration zone
US4734184A (en) * 1985-08-29 1988-03-29 Diamond Sensor Systems, Inc. Self-activating hydratable solid-state electrode apparatus
US4805624A (en) * 1985-09-09 1989-02-21 The Montefiore Hospital Association Of Western Pa Low-potential electrochemical redox sensors
EP0215669A3 (en) 1985-09-17 1989-08-30 Seiko Instruments Inc. Analytical device and method for analysis of biochemicals, microbes and cells
US5500350A (en) * 1985-10-30 1996-03-19 Celltech Limited Binding assay device
US4714874A (en) 1985-11-12 1987-12-22 Miles Inc. Test strip identification and instrument calibration
US4795542A (en) * 1986-04-24 1989-01-03 St. Jude Medical, Inc. Electrochemical concentration detector device
US4703756A (en) 1986-05-06 1987-11-03 The Regents Of The University Of California Complete glucose monitoring system with an implantable, telemetered sensor module
US4731726A (en) * 1986-05-19 1988-03-15 Healthware Corporation Patient-operated glucose monitor and diabetes management system
US4750496A (en) 1987-01-28 1988-06-14 Xienta, Inc. Method and apparatus for measuring blood glucose concentration
US4935346A (en) * 1986-08-13 1990-06-19 Lifescan, Inc. Minimum procedure system for the determination of analytes
US4865873A (en) 1986-09-15 1989-09-12 General Electric Company Electroless deposition employing laser-patterned masking layer
US4897162A (en) * 1986-11-14 1990-01-30 The Cleveland Clinic Foundation Pulse voltammetry
JPH039267Y2 (en) * 1986-12-27 1991-03-07
US4759828A (en) 1987-04-09 1988-07-26 Nova Biomedical Corporation Glucose electrode and method of determining glucose
DE3715938A1 (en) 1987-05-13 1988-11-24 Boehringer Mannheim Gmbh CONTAINER FOR TEST STRIP
US4797256A (en) * 1987-06-05 1989-01-10 Boehringer Mannheim Corporation Registration device for blood test strips
US4812210A (en) * 1987-10-16 1989-03-14 The United States Department Of Energy Measuring surfactant concentration in plating solutions
US4832814A (en) 1987-12-28 1989-05-23 E. I. Du Pont De Nemours And Company Electrofusion cell and method of making the same
US4877580A (en) 1988-02-09 1989-10-31 Technimed Corporation Assay kit including an analyte test strip and a color comparator
US5096669A (en) * 1988-09-15 1992-03-17 I-Stat Corporation Disposable sensing device for real time fluid analysis
AU634863B2 (en) * 1989-12-15 1993-03-04 Roche Diagnostics Operations Inc. Redox mediator reagent and biosensor
US4999582A (en) * 1989-12-15 1991-03-12 Boehringer Mannheim Corp. Biosensor electrode excitation circuit
US4999632A (en) * 1989-12-15 1991-03-12 Boehringer Mannheim Corporation Analog to digital conversion with noise reduction
US5286362A (en) * 1990-02-03 1994-02-15 Boehringer Mannheim Gmbh Method and sensor electrode system for the electrochemical determination of an analyte or an oxidoreductase as well as the use of suitable compounds therefor
US5187100A (en) * 1990-05-29 1993-02-16 Lifescan, Inc. Dispersion to limit penetration of aqueous solutions into a membrane
US5182707A (en) * 1990-07-23 1993-01-26 Healthdyne, Inc. Apparatus for recording reagent test strip data by comparison to color lights on a reference panel
DE4041905A1 (en) * 1990-12-27 1992-07-02 Boehringer Mannheim Gmbh TEST CARRIER ANALYSIS SYSTEM
ES2164641T3 (en) * 1991-02-27 2002-03-01 Roche Diagnostics Corp COMMUNICATION METHOD WITH INSTRUMENTS CONTROLLED BY MICROCOMPUTER.
DE69233262T2 (en) * 1991-02-27 2004-09-30 Roche Diagnostics Corp., Indianapolis Device and method for analyzing body fluids
US5192415A (en) * 1991-03-04 1993-03-09 Matsushita Electric Industrial Co., Ltd. Biosensor utilizing enzyme and a method for producing the same
GB9113211D0 (en) * 1991-06-19 1991-08-07 Hypoguard Uk Ltd Support membrane
US5179288A (en) * 1991-09-30 1993-01-12 Ortho Pharmaceutical Corporation Apparatus and method for measuring a bodily constituent
US5605662A (en) * 1993-11-01 1997-02-25 Nanogen, Inc. Active programmable electronic devices for molecular biological analysis and diagnostics
US5296192A (en) * 1992-04-03 1994-03-22 Home Diagnostics, Inc. Diagnostic test strip
US5389215A (en) * 1992-11-05 1995-02-14 Nippon Telegraph And Telephone Corporation Electrochemical detection method and apparatus therefor
US6168563B1 (en) * 1992-11-17 2001-01-02 Health Hero Network, Inc. Remote health monitoring and maintenance system
US5371687A (en) * 1992-11-20 1994-12-06 Boehringer Mannheim Corporation Glucose test data acquisition and management system
DE59410066D1 (en) * 1993-04-23 2002-04-11 Boehringer Mannheim Gmbh System for analyzing the contents of liquid samples
US5385846A (en) * 1993-06-03 1995-01-31 Boehringer Mannheim Corporation Biosensor and method for hematocrit determination
US5352351A (en) * 1993-06-08 1994-10-04 Boehringer Mannheim Corporation Biosensing meter with fail/safe procedures to prevent erroneous indications
JP2704046B2 (en) * 1993-06-08 1998-01-26 ベーリンガー マンハイム コーポレーション Biosensing meter that detects the appropriate electrode connection and distinguishes between sample and check pieces
US5522255A (en) * 1993-08-31 1996-06-04 Boehringer Mannheim Corporation Fluid dose, flow and coagulation sensor for medical instrument
US5536249A (en) * 1994-03-09 1996-07-16 Visionary Medical Products, Inc. Pen-type injector with a microprocessor and blood characteristic monitor
US6335203B1 (en) * 1994-09-08 2002-01-01 Lifescan, Inc. Optically readable strip for analyte detection having on-strip orientation index
US5597532A (en) * 1994-10-20 1997-01-28 Connolly; James Apparatus for determining substances contained in a body fluid
EP0727925A1 (en) * 1995-02-14 1996-08-21 Lpkf Cad/Cam Systeme Gmbh Process for structured metallizing of the surface of substrates
US6170318B1 (en) * 1995-03-27 2001-01-09 California Institute Of Technology Methods of use for sensor based fluid detection devices
JP3498105B2 (en) * 1995-04-07 2004-02-16 アークレイ株式会社 Sensor, method for manufacturing the same, and measuring method using the sensor
US5873990A (en) * 1995-08-22 1999-02-23 Andcare, Inc. Handheld electromonitor device
AUPN661995A0 (en) * 1995-11-16 1995-12-07 Memtec America Corporation Electrochemical cell 2
US6521110B1 (en) * 1995-11-16 2003-02-18 Lifescan, Inc. Electrochemical cell
US6174420B1 (en) * 1996-11-15 2001-01-16 Usf Filtration And Separations Group, Inc. Electrochemical cell
US5605837A (en) * 1996-02-14 1997-02-25 Lifescan, Inc. Control solution for a blood glucose monitor
US5708247A (en) * 1996-02-14 1998-01-13 Selfcare, Inc. Disposable glucose test strips, and methods and compositions for making same
US6001307A (en) * 1996-04-26 1999-12-14 Kyoto Daiichi Kagaku Co., Ltd. Device for analyzing a sample
DE19621241C2 (en) * 1996-05-25 2000-03-16 Manfred Kessler Membrane electrode for measuring the glucose concentration in liquids
US5719667A (en) * 1996-07-30 1998-02-17 Bayer Corporation Apparatus for filtering a laser beam in an analytical instrument
US5856195A (en) * 1996-10-30 1999-01-05 Bayer Corporation Method and apparatus for calibrating a sensor element
US6013459A (en) * 1997-06-12 2000-01-11 Clinical Micro Sensors, Inc. Detection of analytes using reorganization energy
US6168957B1 (en) * 1997-06-25 2001-01-02 Lifescan, Inc. Diagnostic test strip having on-strip calibration
US6071391A (en) * 1997-09-12 2000-06-06 Nok Corporation Enzyme electrode structure
US6280963B1 (en) * 1997-11-07 2001-08-28 Millennium Pharmaceuticals, Inc. Essential fungal genes and their use
EP2085779B1 (en) * 1997-12-22 2017-11-01 Roche Diagnostics Operations, Inc. Meter
JP3978489B2 (en) * 1998-02-26 2007-09-19 アークレイ株式会社 Blood measuring device
EP0987544B1 (en) * 1998-04-02 2007-10-17 Matsushita Electric Industrial Co., Ltd. Substrate determining method
US6175752B1 (en) * 1998-04-30 2001-01-16 Therasense, Inc. Analyte monitoring device and methods of use
US6526298B1 (en) * 1998-05-18 2003-02-25 Abbott Laboratories Method for the non-invasive determination of analytes in a selected volume of tissue
JP3389106B2 (en) * 1998-06-11 2003-03-24 松下電器産業株式会社 Electrochemical analysis element
US6294281B1 (en) * 1998-06-17 2001-09-25 Therasense, Inc. Biological fuel cell and method
WO1999067019A1 (en) * 1998-06-24 1999-12-29 Therasense, Inc. Combinatorial electrochemical syntheses
US6521182B1 (en) * 1998-07-20 2003-02-18 Lifescan, Inc. Fluidic device for medical diagnostics
US6180416B1 (en) * 1998-09-30 2001-01-30 Cygnus, Inc. Method and device for predicting physiological values
US6338790B1 (en) * 1998-10-08 2002-01-15 Therasense, Inc. Small volume in vitro analyte sensor with diffusible or non-leachable redox mediator
GB9825992D0 (en) * 1998-11-28 1999-01-20 Moorlodge Biotech Ventures Lim Electrochemical sensor
US6193873B1 (en) * 1999-06-15 2001-02-27 Lifescan, Inc. Sample detection to initiate timing of an electrochemical assay
US6514769B2 (en) * 1999-07-29 2003-02-04 Jin Po Lee Multiple analyte assay device with sample integrity monitoring system
US6342364B1 (en) * 1999-11-22 2002-01-29 Matsushita Electric Industrial Co., Ltd. Cholesterol sensor and method of determining cholesterol
JP2001159618A (en) * 1999-12-03 2001-06-12 Matsushita Electric Ind Co Ltd Biosensor
US6706159B2 (en) * 2000-03-02 2004-03-16 Diabetes Diagnostics Combined lancet and electrochemical analyte-testing apparatus
MXPA02009666A (en) * 2000-03-28 2004-07-30 Inverness Medical Technology I Continuous process for manufacture of disposable electro-chemical sensor.
TW548095B (en) * 2000-06-01 2003-08-21 Chih-Hui Lee Electrochemical electrode test piece and method for producing the same
EP1359838A2 (en) * 2000-06-26 2003-11-12 Boston Medical Technologies, Inc. Glucose metering system
DE10032775B4 (en) * 2000-07-06 2007-06-14 Endress + Hauser Gmbh + Co. Kg Device for determining and / or monitoring the fill level of a product in a container
US6561989B2 (en) * 2000-07-10 2003-05-13 Bayer Healthcare, Llc Thin lance and test sensor having same
ES2331689T3 (en) * 2000-07-24 2010-01-13 Panasonic Corporation BIOSENSOR
US6512986B1 (en) * 2000-12-30 2003-01-28 Lifescan, Inc. Method for automated exception-based quality control compliance for point-of-care devices
US6525330B2 (en) * 2001-02-28 2003-02-25 Home Diagnostics, Inc. Method of strip insertion detection
EP1288654B1 (en) * 2001-05-29 2008-10-22 Matsushita Electric Industrial Co., Ltd. Biosensor
US20030036202A1 (en) * 2001-08-01 2003-02-20 Maria Teodorcyzk Methods and devices for use in analyte concentration determination assays
US6689411B2 (en) * 2001-11-28 2004-02-10 Lifescan, Inc. Solution striping system
US6743635B2 (en) * 2002-04-25 2004-06-01 Home Diagnostics, Inc. System and methods for blood glucose sensing
CN1467496A (en) * 2002-06-03 2004-01-14 松下电器产业株式会社 Biosensor

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0537761A2 (en) * 1991-10-18 1993-04-21 Matsushita Electric Industrial Co., Ltd. A biosensor and a method for measuring a concentration of a substrate in a sample
DE19936693A1 (en) * 1999-08-04 2001-02-08 Lre Technology Partner Gmbh Instrument for the measurement of blood sugar concentrations has a test field with electrodes for the test strip and a circuit for measurement/evaluation of the current strength for display
US20020175075A1 (en) * 2001-05-21 2002-11-28 Yingping Deng Electrochemical sensor
EP1275732A1 (en) * 2001-06-11 2003-01-15 Bayer Corporation Electrochemical test sensor with an underfill detection system
WO2003091717A1 (en) * 2002-04-25 2003-11-06 Home Diagnostics, Inc. Systems and methods for blood glucose sensing

Cited By (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10067082B2 (en) 2004-02-06 2018-09-04 Ascensia Diabetes Care Holdings Ag Biosensor for determining an analyte concentration
US9410917B2 (en) 2004-02-06 2016-08-09 Ascensia Diabetes Care Holdings Ag Method of using a biosensor
US8877035B2 (en) 2005-07-20 2014-11-04 Bayer Healthcare Llc Gated amperometry methods
US9835582B2 (en) 2005-09-30 2017-12-05 Ascensia Diabetes Care Holdings Ag Devices using gated voltammetry methods
US9110013B2 (en) 2005-09-30 2015-08-18 Bayer Healthcare Llc Gated voltammetry methods
US10670553B2 (en) 2005-09-30 2020-06-02 Ascensia Diabetes Care Holdings Ag Devices using gated voltammetry methods
US11435312B2 (en) 2005-09-30 2022-09-06 Ascensia Diabetes Care Holdings Ag Devices using gated voltammetry methods
US8647489B2 (en) 2005-09-30 2014-02-11 Bayer Healthcare Llc Gated voltammetry devices
US9274078B2 (en) 2006-03-31 2016-03-01 Lifescan, Inc. Systems and methods of discriminating control solution from a physiological sample
US8529751B2 (en) 2006-03-31 2013-09-10 Lifescan, Inc. Systems and methods for discriminating control solution from a physiological sample
US8449740B2 (en) 2006-03-31 2013-05-28 Lifescan, Inc. Systems and methods for discriminating control solution from a physiological sample
US9005527B2 (en) 2006-10-24 2015-04-14 Bayer Healthcare Llc Transient decay amperometry biosensors
US10190150B2 (en) 2006-10-24 2019-01-29 Ascensia Diabetes Care Holdings Ag Determining analyte concentration from variant concentration distribution in measurable species
US11091790B2 (en) 2006-10-24 2021-08-17 Ascensia Diabetes Care Holdings Ag Determining analyte concentration from variant concentration distribution in measurable species
EP2151682A4 (en) * 2007-04-25 2013-05-15 Arkray Inc Substrate concentration measurement method and substrate concentration measurement apparatus
EP2151682A1 (en) * 2007-04-25 2010-02-10 Arkray, Inc. Substrate concentration measurement method and substrate concentration measurement apparatus
US10347371B2 (en) 2007-05-30 2019-07-09 Ascensia Diabetes Care Holdings Ag Fluid analyte meter system
US9189598B2 (en) 2007-05-30 2015-11-17 Bayer Healthcare Llc Fluid analyte meter
US9157110B2 (en) 2007-09-28 2015-10-13 Lifescan, Inc. Systems and methods of discriminating control solution from a physiological sample
US8778168B2 (en) 2007-09-28 2014-07-15 Lifescan, Inc. Systems and methods of discriminating control solution from a physiological sample
US10690614B2 (en) 2007-12-10 2020-06-23 Ascensia Diabetes Care Holdings Ag Method of using an electrochemical test sensor
US9933385B2 (en) 2007-12-10 2018-04-03 Ascensia Diabetes Care Holdings Ag Method of using an electrochemical test sensor
US8603768B2 (en) 2008-01-17 2013-12-10 Lifescan, Inc. System and method for measuring an analyte in a sample
EP2511698A1 (en) * 2008-01-17 2012-10-17 LifeScan, Inc. Method of identifying an error in performing a test with a test strip
US9739749B2 (en) 2008-01-17 2017-08-22 Lifescan, Inc. System and method for measuring an analyte in a sample
US8916040B2 (en) 2008-01-17 2014-12-23 Lifescan, Inc. System and method for measuring an analyte in a sample
US8709739B2 (en) 2008-01-17 2014-04-29 Lifescan, Inc. System and method for measuring an analyte in a sample
US9784707B2 (en) 2008-06-09 2017-10-10 Lifescan, Inc. System and method for measuring an analyte in a sample
US8551320B2 (en) 2008-06-09 2013-10-08 Lifescan, Inc. System and method for measuring an analyte in a sample
US8617381B2 (en) 2009-06-23 2013-12-31 Bayer Healthcare Llc System and apparatus for determining temperatures in a fluid analyte system
US9097650B2 (en) 2009-06-23 2015-08-04 Bayer Healthcare Llc System and apparatus for determining temperatures in a fluid analyte system
US9664644B2 (en) 2009-06-23 2017-05-30 Ascensia Diabetes Care Holdings Ag System and apparatus for determining temperatures in a fluid analyte system
US10520460B2 (en) 2014-10-27 2019-12-31 Lifescan Ip Holdings, Llc Method for determining diffusion
RU2690065C2 (en) * 2014-10-27 2019-05-30 Цилаг Гмбх Интернэшнл Diffusion determining method

Also Published As

Publication number Publication date
US20040259180A1 (en) 2004-12-23
US7597793B2 (en) 2009-10-06

Similar Documents

Publication Publication Date Title
CA2529668C (en) System and method for analyte measurement using ac excitation
CA2530052C (en) System and method for analyte measurement using dose sufficiency electrodes
EP1639357B1 (en) Method for determining an abused sensor during analyte measurement in a blood sample
US8691152B2 (en) System and method for analyte measurement
US7597793B2 (en) System and method for analyte measurement employing maximum dosing time delay
US7390667B2 (en) System and method for analyte measurement using AC phase angle measurements
EP2344878B1 (en) Identification of control and calibration solutions

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DPEN Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed from 20040101)
122 Ep: pct application non-entry in european phase