WO2000012172A1 - Controlled dosage drug delivery system - Google Patents
Controlled dosage drug delivery system Download PDFInfo
- Publication number
- WO2000012172A1 WO2000012172A1 PCT/US1999/018861 US9918861W WO0012172A1 WO 2000012172 A1 WO2000012172 A1 WO 2000012172A1 US 9918861 W US9918861 W US 9918861W WO 0012172 A1 WO0012172 A1 WO 0012172A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- species
- delivery system
- delivery
- oxidizable
- galvanic
- Prior art date
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0408—Use-related aspects
- A61N1/0428—Specially adapted for iontophoresis, e.g. AC, DC or including drug reservoirs
- A61N1/0432—Anode and cathode
- A61N1/0436—Material of the electrode
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0408—Use-related aspects
- A61N1/0428—Specially adapted for iontophoresis, e.g. AC, DC or including drug reservoirs
- A61N1/0448—Drug reservoir
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0408—Use-related aspects
- A61N1/0428—Specially adapted for iontophoresis, e.g. AC, DC or including drug reservoirs
- A61N1/0432—Anode and cathode
- A61N1/044—Shape of the electrode
Definitions
- the present invention deals generally with transdermal delivery of therapeutic agents by use of an applied electromotive force (emf) , commonly known as iontophoresis. More particularly, the invention is directed to a system for iontophoresis that is self-contained, and quantitatively self-limiting.
- the system is contained preferably in a rather small skin-worn patch which contains electrodes and a therapeutic agent. When applied to the skin, the system completes a circuit and spontaneously initiates the flow of a galvanic current of measured, limited duration corresponding to the desired amount of therapeutic agent to be delivered.
- the system may be anode or cathode limited.
- iontophoresis was described by LeDuc in 1908, and has since found commercial use in the delivery of ionically charged compounds such as pilocarpine, dexamethasone, and lidocaine.
- ions bearing a positive charge are driven across the skin at the site of an electrolytic electrical system anode, while ions bearing a negative charge are driven across the skin at the site of an electrolytic electrical system cathode.
- the application time and level of current flow (usually reported in units of illi- amp minutes) between the anode and cathode is directly correlated to the amount of drug delivered.
- iontophoresis devices conventionally include two electrodes attached to a patient, each connected via a wire to a microprocessor-controlled electrical instrument.
- An illustration of a conventional iontophoretic system is shown in Figure 1. Medication is placed under one or both of the electrodes for delivery into the body as the instrument is activated. The instrument is designed to regulate current flow and application time. Examples of such instruments are described in U.S. Patents 5,254,081 and 5,431,625.
- Power for these devices is usually provided by DC batteries, which when providing power for the microprocessor- controlled circuitry allow application of a voltage to the electrodes to create a regulated current flow.
- the automated control of current flow and time is of great advantage in order to prevent excessive dosages of therapeutic agents from being delivered.
- these battery powered microprocessor- controlled systems are disadvantaged by the fact that patients are attached by wire to an instrument which limits patient mobility and ability to conduct normal daily activities. A typical application period is approximately 20 minutes to 2 hours, which consumes instrument, caregiver and patient time.
- Figure 1 which includes an instrument case 10 for containing a battery-powered current source, a microprocessor- controller, all necessary electronic circuitry and other controls (not shown). An output display is shown at 12.
- Electrode 18 contains a buffer or salt solution at 22 and the electrode 20 is the working electrode containing the medication or therapeutic agent chamber at 24. At all times the patient must remain connected to the device 10 via electrode- connecting wires 26 and 28. All other necessary electronic circuitry for microprocessor-controlled current flow is contained in the instrument case 10.
- wearable iontophoretic systems have been developed in which the electrical circuitry and power supplied are integrated into a single patch. These systems are advantageous in that they do not have external wires, and they are much smaller in size. Examples of such systems can be found in U.S. Patents 5,358,483; 5,458,569; 5,466,217; 5,605,536; and 5,651,768. However, these systems also have the drawback that they are relatively inflexible and expensive, owing to the multiple electronic components, battery power supplies and electrical interconnects.
- Power to drive iontophoretic current flow can also be supplied by galvanic means, which utilizes dissimilar anode and cathode materials to produce a spontaneous current flow when they are contacted with the body.
- galvanic means which utilizes dissimilar anode and cathode materials to produce a spontaneous current flow when they are contacted with the body.
- a primary object of the present invention is to provide a self-contained, self-limiting transdermal iontophoretic drug delivery device.
- Another object of the present invention is to provide a self-contained, self-limiting iontophoretic drug delivery device which is galvanically powered and does not require any separate current source or electric circuitry.
- a further object of the invention is to provide a thin planar, conforming, and relatively small iontophoretic wearable skin patch-type device which does not interfere with the daily activities of the wearer.
- the present invention provides advances in benign transdermal drug delivery.
- the invention provides a self- regulating, wearable iontophoretic system for the transdermal delivery of a therapeutic agent that automatically and inherently provides a controlled or limited amount and controls the rate of delivery.
- the wearable iontophoretic system is preferably in the form of an adhesively applied skin patch which may include a self- sticking hypoallergenic adhesive layer or be taped in place.
- the iontophoretic patch of the invention basically includes two chambers; namely, a cationic drug chamber and an anionic drug chamber.
- the cationic drug chamber contains an electrode which includes material or coating of an electrochemically oxidizable species.
- the anionic drug chamber contains an electrode which likewise includes an electrochemically reducible species.
- the chambers are separated by a known distance and are electrically connected by a conductor.
- any suitable re-dox couple can be used as a battery.
- the oxidizable species and the reducible species preferably are selected so as to provide the desired spontaneous galvanic potential when the iontophoretic patch in which they are contained is in contact with a patient's body.
- the rate of delivery can be adjusted and by adjusting (limiting) the amount of the oxidizable and/or reducible species, the amount of the dosage can be regulated.
- the exemplary embodiments of the iontophoretic wearable patch of the invention further include an impervious backing or top layer which holds the electrodes in place and carries a cell wall defining layer which has two separated openings to define anode and cathode cell cavities.
- Fluid is retained in the cavities by the presence of a hydrophilic absorbent layer which, in turn, may be held in place by a current distribution layer permeable to the passage of drug molecules.
- the patch may further or alternatively have a hypoallergenic adhesive layer also permeable to the passage of drug molecules on the bottom to attach to the skin or be attached utilizing an overlaying bandage material.
- a manual switch or current interrupting device may be provided for use by the patient to interrupt administration of the drug if desired. If desired, an opening may be provided to serve as an inlet for drug-containing fluids which may be injected into the delivery cells just prior to use.
- drug refers to any therapeutic agent susceptible to transdermal delivery in accordance with the principles described herein.
- the backing material may be high density polyethylene tape such as 3M No. 1523 or other occlusive material and the backing material defining the cell walls may be of polyethylene closed cell foam exemplified by 3M No. 1772 or similar material.
- the hydrophilic absorbent layer may include a material which forms a hydrophilic gel when contacted with aqueous solution such as polyacrylamide, or be made from cotton, gauze or other hydrophilic material. Porous membrane material such as nylon, polycarbonate, ethylene vinyl acetate (EVA) and cellulose acetate are examples of suitable materials for use as current distribution layer materials.
- the rate of delivery may be controlled by the electromotive character of the particular electrode materials chosen, and the capacity of the conductor therebetween and the dosage controlled by use of a limited known amount of oxidizable and/or reducible material in the system as the depletion of either will extinguish the galvanic current and so the flow of therapeutic agent.
- an important aspect of the present invention involves the preparation of the iontophoretic electrodes as a known, limiting amount of electro-active species must be associated with either the anode electrode, the cathode electrode or both.
- oxidizable wire or foil material of known weight and purity can be used; or an oxidizable coating of known amount can be deposited on the surface of an electrically conductive substrate.
- a known amount of desired metal can be deposited over a wire or printed circuit substrate to produce an electrode with an oxidizable species of known content.
- any known deposition process involving a particular metal could be used including dipping, electrolytic or electroplating, sputtering, etc.
- a reducible coating of known amount may be deposited on the surface of the other end of the conductor using any known process in preparation of the anionic drug chamber electrode.
- One example of a preferred approach to the preparation of the iontophoretic electrodes of the invention is to dip one end of a silver wire into molten zinc or magnesium and electrolytically generating a known amount of silver chloride on the other end of the wire. Untreated silver wire in the center serves to electrically connect the two electrodes. This process yields a controlled dosage galvanic battery which is thereafter assembled into the iontophoretic patch of the invention.
- the technique involves the ability to deliver any desired designated dosage of a therapeutic agent transdermally to a desired location using a self-contained wearable patch.
- the therapeutic agent may be added at the time of manufacture as by incorporation into the hydrophilic absorbent layers of the drug chambers or may be added by injection into the chambers at the time of use.
- user convenience is improved by eliminating the necessity for the medication adding step.
- Figure 1 is a schematic perspective diagram of a conventional externally-powered iontophoresis device utilizing a connected timer in DC current source;
- Figure 2 depicts a cross-sectional schematic drawing of one embodiment of a wearable patch constructed in accordance with the invention
- Figure 3A is an exploded view showing the assembly of the wearable patch shown in Figure 2;
- Figure 3B is an exploded view showing the assembly of an alternative embodiment of the wearable patch of the invention
- Figure 4 is a schematic diagram illustrating the flow of molecules and electrons in accordance with the electro motive aspects of the wearable patch of the invention
- FIG. 5 illustrates examples of galvanic electrode reactions in accordance with the principles of the present invention
- Figure 6 is a plot of current flow versus time showing the galvanic limiting affect of reducible agent depletion
- Figure 7 graphically depicts the generally linear relationship between the limiting supply of electroplated reducible species (anode limiting) and the capacity of the galvanic battery of the invention
- Figure 8 graphically depicts the generally linear relationship between the limiting supply of oxidizable zinc coating (cathode limiting) and measured galvanic battery capacity in accordance with the invention.
- Figure 9 graphically depicts experimental results showing current flow v. time for a patch made in accordance with the invention as applied to human skin, also depicting the depletion time;
- Figure 10 is a cross-sectional schematic drawing of an alternate embodiment of a wearable patch constructed in accordance with the invention.
- the detailed description of the present invention illustrates the principles of an advanced transdermal drug delivery system.
- the embodiments are described by using a very limited number of example configurations and material compositions, including therapeutic agents delivered. It is believed that the application of the principles encompassed by the present inventive concept, however, are much broader and, in reality, a great number of conductors, galvanic couples (oxidizable and reducible species) , therapeutic agents to be delivered and actual configurations of the wearable patch are possible. Accordingly, the descriptions and accounts given herein are intended as examples and not meant to limit the scope of the invention in any manner.
- the iontophoretic wearable patch of the invention shown generally at 40 includes two chambers; namely, a cationic drug chamber 42 and an anionic drug chamber 44.
- the cationic drug chamber may be described as one containing a return electrode 46 which comprises or otherwise is provided with an electrochemically oxidizable species, such as by a coating on the electrode at 47.
- the anionic drug chamber includes a working electrode 48 which is comprised of or otherwise contains an electrochemically reducible species ,which also may be in the form of a coating at 49.
- the chambers are typically separated by a known distance which is optimally between about 0.1cm and 2cm, keeping in mind that other distances can be used, but that it is desirable to maintain the iontophoretic patches as rather small in size.
- the cationic chamber electrode 46 and the anionic chamber electrode 48 are electrically connected by a conductor at 50 which is typically a common wire ( Figure 3A) .
- Other components of the patch include an impervious non-conducting flexible backing layer 52 which can be constructed using 3M polyethylene tape #1523, or other occlusive material. Holding the electrodes in place and attached to the backing material is a cell wall defining layer 54 which has two separated openings 56 and 58 to define anode and cathode cell or chamber cavities.
- the cell wall defining layer can be constructed of 3M #1772 or similar material.
- a hydrophilic absorbent layer as at 60 is added to each of the cavities defined by the cell wall defining layer and serves to retain fluid in the cell cavity.
- the hydrophilic layer 60 can be a material which forms a hydrophilic gel when contacted with aqueous solution such as polyacrylamide or it can be cotton, gauze, or other hydrophilic material.
- a current distribution layer 62 associated with each cell cavity is one device that serves to hold the hydrophilic absorbent layer in place and is permeable to passage of drug molecules.
- Porous membrane materials such as nylon, polycarbonate, eva, and cellulose acetate are suitable for use as current distribution layer materials.
- Within the porous membrane is a circular opening or inlet port 64 of approximately 4 mm in diameter, which serves as an inlet port for drug containing fluids.
- the current distribution layers 62 are replaced with a hypoallergenic adhesive layer 66 which is also drug permeable.
- a hypoallergenic adhesive layer 66 which is also drug permeable.
- the current distribution layer is optional and can be replaced when other means to secure the hydrophilic absorbent layer in place are provided.
- it may be placed in either the anodic or cathodic chamber.
- the oxidizable species and the reducible species of the galvanic battery or couple are selected so as to provide a spontaneous galvanic potential when the iontophoretic patch is in contact with the body.
- suitable oxidizable species include zinc and magnesium.
- suitable reducible species include silver chloride and cupric oxide.
- zinc is used as the oxidizable species and silver chloride is used as the reducible species
- the galvanic potential established is approximately 1 volt.
- magnesium is used as the oxidizable species and silver chloride is used as the reducible species
- the galvanic potential established is approximately 2.6 volts.
- the oxidizable species in the cationic drug chamber becomes oxidized, while the reducible species in the anionic chamber becomes reduced.
- the galvanically induced current will continue to flow until depletion of either the oxidizable or reducible species, whichever is present in limiting amount.
- the relationship between the amount of current flow and the amount of oxidizable or reducible species in limiting supply, is theoretically represented by Faradays constant; one gram equivalent of the limiting reducible or oxidizable species will provide one Faraday (96,487 coulombs) of electricity.
- the iontophoretic patch of this invention will optimally deliver a fixed and known charge between 0.06 and 60 coulombs, which corresponds to between 0.00000062 and 0.00062 gram equivalent weight of oxidizable or reducible species in limiting supply.
- oxidizable wire or foil material can be used of known weight and purity; or an oxidizable coating of known amount can be deposited on the surface of an electrically conductive substrate.
- a known amount of molten zinc or magnesium can be deposited over a wire substrate to produce an electrode with known oxidizable species content.
- a reducible coating of known amount is deposited on the surface of an electrically conductive substrate.
- a known amount of molten silver chloride can be deposited over a wire substrate to produce an electrode with known reducible species content.
- a known amount of silver chloride can be generated on the electrode surface by an electrolytic or electroplating process, such as by electrolytic oxidation of a silver wire in the presence of chloride, to produce a coating of silver chloride.
- the preferred approach to preparation of the iontophoretic electrodes of this invention is to dip one end of a silver wire into molten zinc or magnesium and electrolytically generate a known amount of silver chloride on the other end of the wire. This process yields a controlled dosage galvanic battery, which is assembled into the iontophoretic patch as shown in Figures 3A and 3B.
- solution containing cation to be delivered is injected into the inlet port of the cationic drug chamber and solution containing anion material is injected into the inlet port of the anionic drug chamber.
- the patch is then applied to the portion of the body where drug is to be administered and adhered to the skin by an adhesive layer on the bottom of the patch and/or by an overlaying bandage material. Once contacted with skin, an electrical circuit is completed which allows passage of current and delivery of drug compounds.
- Figure 4 schematically illustrates the flow of electrons and ions during use of this invention.
- Figure 5 shows electrochemical half reactions which can serve as means to provide stimulation current in this invention. When either the oxidizable material of the cationic chamber electrode is depleted, or the reducible material of the anionic drug chamber electrode is depleted, current flow falls to essentially zero and the delivery of drug compound is completed.
- Figure 6 illustrates the fixed delivery of current as a function of time from a battery prepared in accordance to this invention.
- a zinc wire serves as the oxidizable species and the reducible species was a limiting supply of electroplated silver chloride deposited over a silver wire.
- the zinc and silver chloride ends were placed in a 1% sodium chloride solution and current flow was measured by an ammeter in direct connection. The current measured was steady, then depleted rapidly to near zero after approximately 5 minutes of use.
- FIG 7 results from similar experiments using varying amounts of limiting silver chloride is shown. This illustrates how a limiting supply of the reducible species, silver chloride, can be used to establish and control the battery capacity in the iontophoretic patch of this invention.
- Figure 8 illustrates results similar to that shown in Figure 7 using varying limiting amounts of the oxidizable material, zinc, rather than the reducible species, silver chloride. The figure illustrates how a limiting supply of oxidizable material can be used to establish and control the battery capacity in the iontophoretic patch of the invention in the same manner as the reducible material.
- Figure 9 is an illustration of current flow from a patch produced in accordance with the present invention when applied on human skin using a 1% sodium chloride solution in both chambers.
- zinc of a known quantity was deposited in a limiting amount as the oxidizable species, with silver chloride deposited in excess amount as the reducing species making this battery or cell cathode limited.
- current flow reached approximately 0.1 mA and held relatively steady until the zinc became depleted at about 190 minutes. Thereafter, the current rapidly dropped to near 0.
- FIG. 10 An embodiment is depicted generally at 80 in Figure 10.
- That system includes cathodic drug chamber 82 containing a return electrode 84 having an oxidizable electrode coating 86 and an anodic drug chamber 88 containing a working electrode 90 with a reducible electrode coating 92.
- electrical connecting element 94 that connects the working and return electrodes is provided with a manually operable switch or disconnect device 96 which can be opened to interrupt the galvanic current as shown in the Figure. With the switch 96 closed, of course, the system operates as shown in the embodiment of Figure 2.
- This feature provides an optimal additional level of control to the patient with regard to the administration of a therapeutic agent.
- materials and shapes of wire substrates are possible in creating the galvanic couple or battery for use in the wearable patch of the invention.
- electrically conductive material can be used. These include, for example, copper wire, aluminum wire and/or any type of a printed circuit conductor provided on a non-conducting substrate.
- the techniques for applying both the oxidizable and reducible constituents of the galvanic couple or battery to the conducting substrate are many and others such as icrodispensing, adhesive coating, screen printing, sputtering or the like will also occur to those skilled in the art and any workable process in which the amount of applied material can be regulated are contemplated by this invention. Weighing, of course, is also a viable alternative for determining the amount of material coated on the conducting surface.
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DK99942308T DK1115454T3 (en) | 1998-08-31 | 1999-08-18 | Controlled dose drug delivery system |
EP99942308A EP1115454B1 (en) | 1998-08-31 | 1999-08-18 | Controlled dosage drug delivery system |
DE69933780T DE69933780T2 (en) | 1998-08-31 | 1999-08-18 | CONTROLLED MEDICATION DOSING DEVICE |
JP2000567277A JP4421113B2 (en) | 1998-08-31 | 1999-08-18 | Controlled administration drug delivery system |
US10/166,157 US7031768B2 (en) | 1998-08-31 | 2002-06-10 | Controlled dosage drug delivery |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9865298P | 1998-08-31 | 1998-08-31 | |
US60/098,652 | 1998-08-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000012172A1 true WO2000012172A1 (en) | 2000-03-09 |
Family
ID=22270319
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1999/018861 WO2000012172A1 (en) | 1998-08-31 | 1999-08-18 | Controlled dosage drug delivery system |
Country Status (9)
Country | Link |
---|---|
US (1) | US7031768B2 (en) |
EP (1) | EP1115454B1 (en) |
JP (2) | JP4421113B2 (en) |
AT (1) | ATE343411T1 (en) |
DE (1) | DE69933780T2 (en) |
DK (1) | DK1115454T3 (en) |
ES (1) | ES2279633T3 (en) |
PT (1) | PT1115454E (en) |
WO (1) | WO2000012172A1 (en) |
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Also Published As
Publication number | Publication date |
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DE69933780T2 (en) | 2007-09-13 |
DK1115454T3 (en) | 2007-02-19 |
JP2007014791A (en) | 2007-01-25 |
DE69933780D1 (en) | 2006-12-07 |
EP1115454A1 (en) | 2001-07-18 |
US20030028170A1 (en) | 2003-02-06 |
JP2002523194A (en) | 2002-07-30 |
JP4619333B2 (en) | 2011-01-26 |
JP4421113B2 (en) | 2010-02-24 |
ATE343411T1 (en) | 2006-11-15 |
EP1115454A4 (en) | 2004-06-30 |
ES2279633T3 (en) | 2007-08-16 |
US7031768B2 (en) | 2006-04-18 |
PT1115454E (en) | 2007-01-31 |
EP1115454B1 (en) | 2006-10-25 |
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