WO2002043785A2 - Intraocular implants for preventing transplant rejection in the eye - Google Patents
Intraocular implants for preventing transplant rejection in the eye Download PDFInfo
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- WO2002043785A2 WO2002043785A2 PCT/US2001/044481 US0144481W WO0243785A2 WO 2002043785 A2 WO2002043785 A2 WO 2002043785A2 US 0144481 W US0144481 W US 0144481W WO 0243785 A2 WO0243785 A2 WO 0243785A2
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- bioerodible
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- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
- A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
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- A61F9/00—Methods or devices for treatment of the eyes; Devices for putting-in contact lenses; Devices to correct squinting; Apparatus to guide the blind; Protective devices for the eyes, carried on the body or in the hand
- A61F9/0008—Introducing ophthalmic products into the ocular cavity or retaining products therein
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- A61F9/00—Methods or devices for treatment of the eyes; Devices for putting-in contact lenses; Devices to correct squinting; Apparatus to guide the blind; Protective devices for the eyes, carried on the body or in the hand
- A61F9/0008—Introducing ophthalmic products into the ocular cavity or retaining products therein
- A61F9/0017—Introducing ophthalmic products into the ocular cavity or retaining products therein implantable in, or in contact with, the eye, e.g. ocular inserts
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Definitions
- This invention relates to the field of transplantation, in particular transplantation of components of the eye, and methods for preventing transplant rejection.
- Certain conditions and diseases of the eye such as corneal failure, keratoconus, corneal dystrophies, scarring, age related macular degeneration (AMD) and retinitis pigmentosa, have been treated using ocular transplant procedures such as corneal and retinal pigment epithelial (RPE) transplants.
- Transplant rejection is one of the problems which may arise from transplant procedures (Enzmann V et al. (1998).
- One embodiment of the present invention provides a method for reducing or preventing transplant rejection in the eye of an individual, where the method comprises: a) performing an ocular transplant procedure; and b) implanting in the eye a bioerodible drug delivery system comprising an immunosuppressive agent and a bioerodible polymer.
- Another embodiment of the invention provides a method for reducing or preventing transplant rejection in the eye of an individual, where the method comprises: a) performing an ocular transplant procedure; and b) implanting a solid body into the eye, said body comprising particles of an immunosuppressive agent entrapped within a bioerodible polymer, whereby said agent is released from the body by erosion of the polymer.
- Another embodiment of the invention provides a method which includes placing in an eye of an individual a bioerodible drug delivery system, where the bioerodible drug delivery system includes an immunosuppressive agent and a bioerodible polymer; and where the eye of the individual has undergone or is undergoing an ocular transplant procedure. This method may be used to reduce or prevent transplant rejection.
- Another embodiment of the invention provides a kit comprising: a) a bioerodible drug delivery system comprising an immunosuppressive agent and a bioerodible polymer, wherein the drug delivery system is designed to be implanted in the eye; and b) instructions for use. This kit may be used to reduce or prevent transplant rejection.
- ocular transplant procedure refers to any transplant procedure performed in the eye.
- Non-limiting examples of ocular transplant procedures include, but are not limited to, retinal pigment epithelium (RPE) transplant and cornea transplant. It includes autograft, allograft and xenograft transplant procedures.
- RPE retinal pigment epithelium
- Immunosuppressive agent "agent”
- Immunosuppressive drug and
- drug are used interchangeably herein, and refer to any agent which inhibits or prevents an immune response against the transplanted tissue following a transplant procedure.
- exemplary agents include, but are not limited to, dexamethasone, cyclosporin A, azathioprine, brequinar, gusperimus, 6-mercaptopurine, mizoribine, rapamycin, tacrolimus
- folic acid analogs e.g., denopterin, edatrexate, methotrexate, piritrexim, pteropterin, Tomudex®, trimetrexate
- purine analogs e.g., cladribine, fludarabine, 6- mercaptopurine, thiamiprine, thiaguanine
- pyrimidine analogs e.g., ancitabine, azacitidine, 6-azauridine, carmofur, cytarabine, doxifluridine, emitefur, enocitabine, floxuridine, fluorouracil, gemcitabine, tegafur
- fluocinolone triaminolone, anecortave acetate, flurometholone, medrysone, and prednislone.
- an “implant” and a “drug delivery system,” are used interchangeably herein, and include any bioerodible device for implantation in the eye which is capable of delivering a therapeutic level of drug to the eye.
- terapéutica level is meant a level of drug sufficient to prevent, inhibit, or reduce the level of transplant rejection in the eye.
- bioerodible polymer refers to polymers which degrade in vivo, and wherein erosion of the polymer over time is required to achieve the agent release kinetics according to the invention.
- hydrogels such as methylcellulose which act to release drug through polymer swelling are specifically excluded from the term
- bioerodible polymer The terms “bioerodible” and “biodegradable” are equivalent and are used interchangeably in this patent.
- mammals include, but are not limited to, humans, rodents, sport animals and pets, such as rats, dogs, and horses.
- Intraocular immunosuppressive drug delivery systems made of a biodegradable polymer matrix are provided which can release drug loads over various programmed time periods. When inserted into the eye these drug delivery systems provide therapeutic levels of immunosuppressive agent for reducing or preventing transplant rejection.
- one embodiment of the present invention provides a method for reducing or preventing transplant rejection in the eye of an individual, comprising: performing an ocular transplant procedure; and implanting in the eye a bioerodible drug delivery system comprising an immunosuppressive agent and a bioerodible polymer.
- a method for reducing or preventing transplant rejection in the eye of an individual comprising: performing an ocular transplant procedure; and implanting a solid body into the eye, said body comprising particles of an immunosuppressive agent entrapped within a bioerodible polymer, whereby said agent is released from the body by erosion of the polymer.
- Ocular transplant procedures which may be used with the methods of the invention include, but are not limited to, cornea transplant and RPE transplant. Methods for performing these transplant procedures are well known in the art. Methods for performing RPE transplants are described in, for example, U.S. Pat. Nos. 5,962,027, 6,045,791 , and 5,941 ,250 and in Eye Graefes Arch Clin Exp Opthalmol 1997 Mar; 235(3): 149-58; Biochem Biophys Res Commun 2000 Feb 24; 268(3): 842-6; Opthalmic Surg 1991 Feb; 22(2): 102-8. Methods for performing corneal transplants are described in, for example, U.S. Pat. No.
- the ocular transplant procedure is a cornea transplant.
- the ocular transplant procedure is an RPE procedure.
- the drug delivery system may be implanted at various sites in the eye, depending on the size, shape and formulation of the implant, the type of transplant procedure, etc. Suitable sites include but are not limited to the anterior chamber, anterior segment, posterior chamber, posterior segment, vitreous cavity, suprachoroidal space, subconjunctiva, episcleral, intracomeal, epicorneal and sclera.
- the drug delivery system is placed in the anterior chamber of the eye.
- the drug delivery system is placed in the vitreous cavity.
- the implants may be inserted into the eye by a variety of methods, including placement by forceps or by trocar following making an incision in the sclera (for example, a 2-3 mm incision) or other suitable site.
- the implant may be able to be placed by trocar without making a separate incision, but instead by punching a hole directly into the eye with the trocar.
- the method of placement may influence the drug release kinetics. For example, implanting the device into the vitreous with a trocar may result in placement of the device deeper within the vitreous than placement by forceps, which may result in the implant being closer to the edge of the vitreous.
- the location of the implanted device may influence the concentration gradients of drug surrounding the device, and thus influence the release rates (e.g., a device placed closer to the edge of the vitreous may result in a slower release rate).
- U.S. Pat. No. 5,869,079 further describes locations for intraocular implants and methods for insertion (see in particular col. 6-7).
- the implant delivers the immunosuppressive agent for at least about 5 days. In other embodiments, the implant delivers the immunosuppressive agent for at least about one week, at least about 2 weeks, at least about 3 weeks, at least about four weeks, at least about five weeks, at least about six weeks, at least about seven weeks, at least about eight weeks, at least about nine weeks, at least about 10 weeks, and at least about 12 weeks.
- the preferred duration of drug release may be determined by the type of transplant, the medical history of the patient, etc. In one embodiment, drug release may occur for up to 6 months, or one year, or longer. In one embodiment, more than one implant may be sequentially implanted into the vitreous in order to maintain drug concentrations for even longer periods.
- more than one implant may be sequentially implanted into the eye in order to maintain therapeutic drug concentrations for longer periods.
- the methods of the invention are preferably performed on vertebrates, preferably mammal, more preferably a human. Mammals include, but are not limited to, humans, rodents, sport animals and pets, such as rats, dogs and horses.
- the formulation of the implants for use in the invention may vary according to the preferred drug release profile, the particular immunosuppressive agent used, the transplant procedure, the medical history of the patient and other factors affecting the formulation.
- the implants of the invention are formulated with particles of the immunosuppressive agent associated with the bioerodible polymer matrix.
- the immunosuppressive agent is entrapped within the bioerodible polymer matrix.
- release of the agent is achieved by erosion of the polymer followed by exposure of previously entrapped agent particles to the eye, and subsequent dissolution and release of agent.
- the release kinetics achieved by this form of drug release are different than that achieved through formulations which release drug through polymer swelling, such as with hydrogels such as methylcellulose. In that case, the drug is not released through polymer erosion, but through polymer swelling, which release drug as liquid diffuses through the pathways exposed.
- the parameters which may determine the release kinetics include the size of the drug particles, the water solubility of the drug, the ratio of drug to polymer, the method of manufacture, the surface area exposed, and the erosion rate of the polymer.
- the immunosuppressive agent is selected from the group consisting of dexamethasone, cyclosporin A, azathioprine, brequinar, gusperimus, 6-mercaptopurine, mizoribine, rapamycin, tacrolimus (FK-506), folic acid analogs (e.g., denopterin, edatrexate, methotrexate, piritrexim, pteropterin, Tomudex®, trimetrexate), purine analogs (e.g., cladribine, fludarabine, 6-mercaptopurine, thiamiprine, thiaguanine), pyrimidine analogs (e.g., ancitabine, azacitidine, 6-azauridine, carmofur, cytarabine, doxifluridine, emitefur, enocitabine, floxuridine, fluorouracil, gemcitabine, tegafur) fluo
- the immunosuppressive agent is cyclosporin A.
- the bioerodible implant comprises more than one immunosuppressive agent.
- the implants may further comprise one or more additional therapeutic agents, such as antibiotics or antiinflammatory agents.
- additional therapeutic agents such as antibiotics or antiinflammatory agents.
- antibiotics include, but are not limited to:
- Aminoglycosides e.g., amikacin, apramycin, arbekacin, bambermycins, butirosin, dibekacin, dihydrostreptomycin, fortimicin(s), gentamicin, isepamicin, kanamycin, micronomicin, neomycin, neomycin undecylenate, netilmicin, paromomycin, ribostamycin, sisomicin, spectinomycin, streptomycin, tobramycin, trospectomycin), amphenicols (e.g., azidamfenicol, chloramphenicol, florfenicol, thiamphenicol), ansamycins (e.g., rifamide, rifampin, rifamycin sv, rifapentine, rifaximin), ⁇ -lactams (e.g., carbacephems (e.g.
- 2,4-Diaminopyrimidines e.g., brodimoprim, tetroxoprim, trimethoprim
- nitrofurans e.g., furaltadone, furazolium chloride, nifuradene, nifuratel, nifurfoline, nifurpirinol, nifurprazine, nifurtoinol, nitrofurantoin
- quinolones and analogs e.g., cinoxacin, ciprofloxacin, clinafloxacin, difloxacin, enoxacin, fleroxacin, flumequine, grepafloxacin, lomefloxacin, miloxacin, nadifloxacin, nalidixic acid, norfloxacin, ofloxacin, oxolinic acid, pazufloxacin, pefloxacin, pipemidic acid, piromidic
- Polyenes e.g. , amphotericin b, candicidin, dermostatin, filipin, fungichromin, hachimycin, hamycin, lucensomycin, mepartricin, natamycin, nystatin, pecilocin, perimycin
- others e.g., azaserine, griseofulvin, oligomycins, neomycin undecylenate, pyrrolnitrin, siccanin, tubercidin, viridin.
- Allylamines e.g. , butenafine, naftifine, terbinafine
- imidazoles e.g. , bifonazole, butoconazole, chlordantoin, chlormidazole, cloconazole, clotrimazole, econazole, enilconazole, fenticonazole, flutrimazole, isoconazole, ketoconazole, lanoconazole, miconazole, omoconazole, oxiconazole nitrate, sertaconazole, sulconazole, tioconazole), thiocarbamates (e.g., tolciclate, tolindate, tolnaftate), triazoles (e.g., fluconazole, itraconazole, saperconazole, terconazole) others (e.g., acrisorcin, amorolfine, biphenamine,
- Antibiotics and analogs e.g., aclacinomycins, actinomycin f l5 anthramycin, azaserine, bleomycins, cactinomycin, carubicin, carzinophilin, chromomycins, dactinomycin, daunorubicin, 6-diazo-5-oxo-L-norleucine, doxorubicin, epirubicin, idarubicin, menogaril, mitomycins, mycophenolic acid, nogalamycin, olivomycines, peplomycin, pirarubicin, plicamycin, porfiromycin, puromycin, streptonigrin, streptozocin, tubercidin, zinostatin, zorubicin), antimetabolites (e.g., aclacinomycins, actinomycin f l5 anthramycin, azaserine, bleomycins, cactinomycin
- folic acid analogs e.g., denopterin, edatrexate, methotrexate, piritrexim, pteropterin, Tomudex ® , trimetrexate
- purine analogs e.g., cladribine, fludarabine, 6-mercaptopurine, thiamiprine, thioguanine
- pyrimidine analogs e.g., ancitabine, azacitidine, 6-azauridine, carmofur, cytarabine, doxifluridine, emitefur, enocitabine, floxuridine, fluorouracil, gemcitabine, tagafur.
- Specific antiinflammatory agents include, but are not limited to: Steroidal antiinflammatory agents:
- Non-steroidal antiinflammatory agents are non-steroidal antiinflammatory agents.
- Aminoarylcarboxylic acid derivatives e.g., enfenamic acid, etofenamate, flufenamic acid, isonixin, meclofenamic acid, mefenamic acid, niflumic acid, talniflumate, terofenamate, tolfenamic acid
- arylacetic acid derivatives e.g., aceclofenac, acemetacin, alclofenac, amfenac, amtolmetin guacil, bromfenac, bufexamac, cinmetacin, clopirac, diclofenac sodium, etodolac, felbinac, fenclozic acid, fentiazac, glucametacin, ibufenac, indomethacin, isofezolac, isoxepac, lonazolac, metiazinic acid, mofezolac, ox
- arylpropionic acid derivatives e.g., alminoprofen, benoxaprofen, bermoprofen, bucloxic acid, carprofen, fenoprofen, flunoxaprofen, flurbiprofen, ibuprofen, ibuproxam, indoprofen, ketoprofen, loxoprofen, naproxen, oxaprozin, piketoprolen, pirprofen, pranoprofen, protizinic acid, suprofen, tiaprofenic acid, ximoprofen, zaltoprofen), pyrazoles (e.g., difenamizole, epirizole), pyrazolones (e.g., apazone, benzpiperylon, feprazone, mofebutazone, morazone,
- 3-amino-4-hydroxybutyric acid amixetrine, bendazac, benzydamine, ⁇ -bisabolol, bucolome, difenpiramide, ditazol, emorfazone, fepradinol, guaiazulene, nabumetone, nimesulide, oxaceprol, paranyline, perisoxal, proquazone, superoxide dismutase, tenidap, and zileuton.
- the immunosuppressive agent is preferably from about 10 to 90% by weight of the implant. More preferably, the agent is from about 50 to about 80% by weight of the implant. In a preferred embodiment, the agent comprises about 50% by weight of the implant. In a preferred embodiment, the agent comprises about 70% by weight of the implant.
- the implants are preferably monolithic, i.e. having the immunosuppressive agent homogeneously distributed through the polymeric matrix.
- immunosuppressive agent is distributed evenly enough that no detrimental fluctuations in rate of immunosuppressive agent release occur because of uneven distribution of the immunosuppressive agent in the polymer matrix.
- the selection of the polymeric composition to be employed will vary with the desired release kinetics, the location of the implant, patient tolerance, the nature of the transplant procedure and the like. Characteristics of the polymers will include biodegradabihty at the site of implantation, compatibility with the agent of interest, ease of encapsulation, water insolubility, and the like.
- the polymeric matrix will not be fully degraded until the drug load has been released.
- the polymer will usually comprise at least about 10, more usually at least about 20 weight percent of the implant.
- the implant comprises more than one polymer.
- Biodegradable polymeric compositions which may be employed may be organic esters or ethers, which when degraded result in physiologically acceptable degradation products, including the monomers. Anhydrides, amides, orthoesters or the like, by themselves or in combination with other monomers, may find use.
- the polymers may be condensation polymers.
- the polymers may be cross-linked or non-cross-linked, usually not more than lightly cross-linked, generally less than 5%, usually less than 1% cross-linked.
- the polymers will include oxygen and nitrogen, particularly oxygen.
- the oxygen may be present as oxy, e.g.
- biodegrable polymers set forth in Heller, Biodegrable Polymers in Controlled Drug Delivery, in: CRC Critical
- polyesters of interest include polymers of D-lactic acid, L-lactic acid, racemic lactic acid, glycolic acid, polycaprolactone, and combinations thereof.
- L-lactate or D-lactate a slowly biodegrading polymer is achieved, while degradation is substantially enhanced with the racemate.
- Copolymers of glycolic and lactic acid are of particular interest, where the rate of biodegradation is controlled by the ratio of glycolic to lactic acid.
- the % of polylactic acid in the polylactic acid polyglycolic acid (PLGA) copolymer can be 0-100%, preferably about 15-85%, more preferably about 35-65%. In a particularly preferred embodiment, a 50/50 PLGA copolymer is used.
- the most rapidly degraded copolymer has roughly equal amounts of glycolic and lactic acid, where either homopolymer is more resistant to degradation.
- the ratio of glycolic acid to lactic acid will also affect the brittleness of in the implant, where a more flexible implant is desirable for larger geometries.
- the size of the polymer particles is preferably about 1-100 ⁇ m in diameter, more preferably about 5-50 ⁇ m in diameter, more preferably about 9-12 ⁇ m in diameter, still more preferably about 10 ⁇ m in diameter.
- the implant comprises hydroxypropyl methylcellulose (HPMC).
- release modulators such as those described in U.S. Patent No.
- 5,869,079 may be included in the implants.
- the amount of release modulator employed will be dependent on the desired release profile, the activity of the modulator, and on the release profile of the immunosuppressive agent in the absence of modulator.
- Other agents may be employed in the formulation for a variety of purposes.
- buffering agents and preservatives may be employed.
- Water soluble preservatives which may be employed include sodium bisulfite, sodium bisulfate, sodium thiosulfate, benzalkonium chloride, chlorobutanol, thimerosal, phenylmercuric acetate, phenylmercuric nitrate, methylparaben, polyvinyl alcohol and phenylethyl alcohol. These agents may be present in individual amounts of from about 0.001 to about 5% by weight and preferably about 0.01 to about 2%.
- Suitable water soluble buffering agents that may be employed are sodium carbonate, sodium borate, sodium phosphate, sodium acetate, sodium bicarbonate, etc., as approved by the FDA for the desired route of administration. These agents may be present in amounts sufficient to maintain a pH of the system of between 2 to 9 and preferably 4 to 8. As such the buffering agent may be as much as 5% on a weight to weight basis of the total composition. Electrolytes such as sodium chloride and potassium chloride may also be included in the formulation. Where the buffering agent or enhancer is hydrophilic, it may also act as a release accelerator. Hydrophilic additives act to increase the release rates through faster dissolution of the material surrounding the drug particles, which increases the surface area of the drug exposed, thereby increasing the rate of drug bioerosion. Similarly, a hydrophobic buffering agent or enhancer dissolve more slowly, slowing the exposure of drug particles, and thereby slowing the rate of drug bioerosion.
- the proportions of immunosuppressive agent, polymer, and any other modifiers may be empirically determined by formulating several implants with varying proportions.
- a USP approved method for dissolution or release test can be used to measure the rate of release (USP 23; NF 18 (1995) pp. 1790-1798).
- USP 23; NF 18 (1995) pp. 1790-1798 For example, using the infinite sink method, a weighed sample of the drug delivery system is added to a measured volume of a solution containing 0.9% NaCl in water, where the solution volume will be such that the drug concentration is after release is less than 5% of saturation. The mixture is maintained at 37°C and stirred slowly to maintain the implants in suspension.
- the appearance of the dissolved drug as a function of time may be followed by various methods known in the art, such as spectrophotometrically, HPLC, mass spectroscopy, etc. until the absorbance becomes constant or until greater than 90% of the drug has been released.
- the release kinetics of the drug delivery systems of the invention are dependent in part on the surface area of the implants. Larger surface area exposes more polymer to the eye, causing faster erosion and dissolution of the drug particles entrapped by the polymer.
- the size and form of the implant can be used to control the rate of release, period of treatment, and drug concentration at the site of implantation. Larger implants will deliver a proportionately larger dose, but depending on the surface to mass ratio, may have a slower release rate.
- the implants may be particles, sheets, patches, plaques, films, discs, fibers, microcapsules and the like and may be of any size or shape compatible with the selected site of insertion, as long as the implants have the desired release kinetics.
- the implant to be inserted is formulated as a single particle.
- the implant will not migrate from the insertion site following implantation.
- the upper limit for the implant size will be determined by factors such as the desired release kinetics, location of the implant in the eye, toleration for the implant, size limitations on insertion, ease of handling, etc.
- the vitreous chamber is able to accommodate relatively large implants of varying geometries, having diameters of 1 to 3 mm.
- the implant is a cylindrical pellet (e.g., rod) with dimensions of about 2mm x 0.75mm diameter.
- the implant is a cylindrical pellet (e.g., rod) with dimensions of about 1 mm x 380 ⁇ m diameter.
- the implants will also preferably be at least somewhat flexible so as to facilitate both insertion of the implant in the eye and accommodation of the implant.
- the total weight of the implant is preferably about 50-5000 ⁇ g, more preferably about 100-1000 ⁇ g. In one embodiment, the implant is about 500 ⁇ g. In a particularly preferred embodiment, the implant is about 1000 ⁇ g. In another particularly preferred embodiment, the implant is about 120 ⁇ g.
- U.S. Pat. No. 5,869,079 further describes preferred implant sizes for particular regions of the eye, as well as preferred sizes for particular implant shapes.
- a solid bioerodible implant for reducing or preventing transplant rejection in the eye comprising about 50% by weight of dexamethasone, about 15% by weight of hydroxypropyl methylcellulose (HPMC) and about 35% by weight of polylactic polyglycolic acid (PLGA).
- HPMC hydroxypropyl methylcellulose
- PLGA polylactic polyglycolic acid
- a solid bioerodible implant for reducing or preventing transplant rejection in the eye comprising about 70% by weight of dexamethasone and about 30% by weight of polylactic polyglycolic acid (PLGA).
- a solid bioerodible implant for reducing or preventing transplant rejection in the eye comprising about 50% by weight of dexamethasone and about 50% by weight of polylactic polyglycolic acid (PLGA).
- the preferred supplier of PLGA is Boehringer Ingelheim and the preferred
- PLGA products are Resomer RG 502 and Resomer RG 502H.
- the solid bioerodible implant includes about
- the solid bioerodible implant includes about
- Useful techniques include phase separation methods, interfacial methods, extrusion methods, compression methods, molding methods, injection molding methods, heat press methods and the like.
- compression methods are used to produce the implants of the invention.
- compression methods use pressures of 50-150 psi, more preferably about 70-80 psi, even more preferably about 76 psi, and use temperatures of about 0°C to about 115°C, more preferably about 25°C.
- extrusion methods are used.
- implants produced by extrusion methods are heated to a temperature range of about 60°C to about 150°C for drug/polymer mixing, preferably about 85°C, preferably about 130°C, for a time period of about 0 to 1 hour, 0 to 30 minutes, 5-15 minutes, preferably about 10 minutes, preferably about 0 to 5 min, preferably about 1 hour.
- the implants are then extruded at a temperature of about 60°C to about 130°C, preferably about 95°C, preferably about 85°C, preferably about 75°C.
- kits for treating or preventing transplant rejection in the eye comprising a bioerodible drug delivery system comprising an immunosuppressive agent and a bioerodible polymer, wherein the drug delivery system is designed to be implanted in the eye.
- the kit may also include instructions for use.
- the bioerodible drug delivery systems as described herein are suitable for use in the kits of the invention.
- the immunosuppressive agent is dexamethasone.
- the invention is further described by the following nonlimiting examples.
- Example 1 Effect of dexamethasone implant in animal penetrating keratoplasty model.
- the objective of this study was to determine the efficacy of sustained release intraocular dexamethasone implanted in the anterior chamber of the rat eye at the end of cornea transplant surgery and compare it with local eye drop therapy.
- the approximately 120 ⁇ g dexamethasone implant contained about 15% HPMC, 35% PLGA and 50% dexamethasone, and was prepared and tested in vitro as described in U.S. Patent No. 5,869,079 (See Example 1), which is specifically incorporated herein by reference in its entirety.
- PGP Penetrating keratoplasty
- Group #3 heavy inflammation was observed in AC, cornea endothelium, also in the stroma, and some in the epithelium. Corneas also showed edema due to destroyed endothelial cells. [00072] In Group #2 similar findings were observed.
- dexamethasone powder (Upjohn) (particle sizes less than 10 ⁇ m in diameter) were mixed with 900 mg of 50/50 polylactic acid polyglycolic acid (PLGA) (particle sizes approximately 9-12 ⁇ m in diameter) at ambient temperature.
- PLGA polylactic acid polyglycolic acid
- a small Teflon® tube was filled with 900-1100 ⁇ g of the above mixture, and placed directly on the die cavity. The powder was pushed out of the tubing into the die cavity with a stainless steel wire and the tube and wire were removed from the die. The powder was pressed using a tablet press (approximately 76 psi), ejected with the ejector switch, and removed with tweezers. The resulting pellet was approximately 2mm x 0.75mm. [00076] Release of dexamethasone from the DEX PS DDS® system was measured.
- One DDS was placed in a glass vial filled with receptor medium (0.9% NaCl in water).
- receptor medium (0.9% NaCl in water).
- the receptor medium volume was chosen so that the concentration would never exceed 5% of saturation.
- the glass vial was placed into a shaking water bath at 37°C. Samples were taken for HPLC analysis from the vial at defined time points. The HPLC method was as described in USP 23(1995) pp.1791 -1798. The concentration values were used to calculate the cumulative release data, as shown in Table 2.
- Table 2 shows an almost linear in vitro release of dexamethasone over a one month period of time.
- the data indicate that the DEX PS DDS® releases dexamethasone to the vitreous in concentrations above 0.01 ⁇ g/ml for an extended period of time. Further, the data indicate that placement of the device with trocar results in much higher levels of drug release than with placement with forceps, most likely due to placement of the device deeper within the vitreous. The data at two, four, six, and 24 hours in Table 4 shows an initial spike of drug release.
- Example 4 Manufacture And In vitro Testing Of 50/50 Dexamethasone PLGA Posterior Segment Drug Delivery System
Abstract
Description
Claims
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE60114229T DE60114229T2 (en) | 2000-11-29 | 2001-11-28 | PREVENTING TRANSPLANT DISCHARGE IN THE EYE |
BR0115772-8A BR0115772A (en) | 2000-11-29 | 2001-11-28 | Processes for reducing or preventing eye transplant rejection and intraocular implants for use in transplantation |
AU2002236495A AU2002236495B2 (en) | 2000-11-29 | 2001-11-28 | Intraocular implants for preventing transplant rejection in the eye |
AU3649502A AU3649502A (en) | 2000-11-29 | 2001-11-28 | Methods for reducing or preventing transplant rejection in the eye and intraocular implants for use therefor |
JP2002545755A JP2004514702A (en) | 2000-11-29 | 2001-11-28 | Intraocular implant for preventing transplant rejection in the eye |
CA2429998A CA2429998C (en) | 2000-11-29 | 2001-11-28 | Intraocular implants for preventing transplant rejection in the eye |
EP01986027A EP1339438B1 (en) | 2000-11-29 | 2001-11-28 | Preventing transplant rejection in the eye |
AT01986027T ATE306951T1 (en) | 2000-11-29 | 2001-11-28 | PREVENTING TRANSPLANT REJECTION IN THE EYE |
AU2006201271A AU2006201271B2 (en) | 2000-11-29 | 2006-03-28 | Intraocular implants for preventing transplant rejection in the eye |
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US25002300P | 2000-11-29 | 2000-11-29 | |
US60/250,023 | 2000-11-29 | ||
US29825301P | 2001-06-12 | 2001-06-12 | |
US60/298,253 | 2001-06-12 |
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US (16) | US6699493B2 (en) |
EP (1) | EP1339438B1 (en) |
JP (3) | JP2004514702A (en) |
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AU (3) | AU2002236495B2 (en) |
BR (1) | BR0115772A (en) |
CA (1) | CA2429998C (en) |
DE (1) | DE60114229T2 (en) |
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