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Publication numberUS20040067301 A1
Publication typeApplication
Application numberUS 10/679,057
Publication dateApr 8, 2004
Filing dateOct 3, 2003
Priority dateJul 7, 1998
Also published asCA2336650A1, CA2336650C, DE1096902T1, DE69938047D1, EP1096902A1, EP1096902B1, US6652581, US7758909, US20070299509, WO2000001322A1
Publication number10679057, 679057, US 2004/0067301 A1, US 2004/067301 A1, US 20040067301 A1, US 20040067301A1, US 2004067301 A1, US 2004067301A1, US-A1-20040067301, US-A1-2004067301, US2004/0067301A1, US2004/067301A1, US20040067301 A1, US20040067301A1, US2004067301 A1, US2004067301A1
InventorsNi Ding
Original AssigneeSchneider (Usa), Inc.
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Medical device with porous surface for controlled drug release and method of making the same
US 20040067301 A1
Abstract
The medical devices of the invention comprise a portion having a porous surface for release of at least one biologically active agent therefrom. The porous surface is made of a material such as a polymer having a plurality of voids. To load the porous surface with a biologically active agent or drug, an electrophoresis method is employed. In this method, a device having a porous surface is placed into a drug solution or suspension, along with an electrode. An electric current is applied to the device and electrode. Under such a current, the drug, which has a positive or negative charge, will be loaded into the pores or voids of the porous surface.
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Claims(28)
I claim:
1. A method of making a medical device having at least a portion for insertion or implantation into the body of a patient, wherein the-portion has a surface which is adapted for exposure to body tissue of the patient and wherein at least a part of the surface is a porous surface having a plurality of voids therein to release at least one biologically active agent therefrom, the method comprising loading the porous surface with the biologically active agent by
a) forming a solution or suspension of the biologically active agent,
b) placing the device into the solution or suspension,
c) placing an electrode in the solution or suspension,
d) applying an electric current to the device and the electrode, and
e) allowing at least some of the biologically active agent to be loaded into the voids.
2. The method of claim 1 wherein the device comprises at least a metal portion.
3. The method of claim 1 wherein the electrode functions as a cathode and the biologically active agent has a negative charge.
4. The method of claim 1 wherein the electrode functions as an anode and the biologically active agent has a positive charge.
5. The method of claim 1 wherein the device is a stent.
6. The method of claim 5 wherein the stent comprises a metallic material.
7. The method of claim 6 wherein the stent is a self-expanding stent.
8. The method of claim 6 wherein the stent is a balloon-expandable stent.
9. The method of claim 1 wherein the device is a stent graft.
10. The method of claim 9 wherein the stent graft comprises a metallic material.
11. The method of claim 1 wherein the biologically active agent is heparin.
12. The method of claim 1 wherein the biologically active agent is loaded immediately before implantation of the device.
13. The method of claim 1 wherein at least some of the voids contain a particulate material prior to placing the device into the solution or suspension.
14. A method of making a medical device having at least a portion for insertion or implantation into the body of a patient, wherein the portion has a surface which is adapted for exposure to body tissue of the patient and wherein at least a part of the surface is covered with a porous coating having a plurality of voids for release of at least one biologically active agent therefrom, the method comprising:
a) forming the porous coating on the surface by
i) applying a composition comprising a polymer and a particulate material to the surface and
ii) exposing the surface to a solvent to elute the particulate material from the polymer; and
b) loading the porous coating with the biologically active agent by
i) forming a solution or suspension of the biologically active agent,
ii) placing the coated device into the solution or suspension,
iii) placing an electrode in the solution or suspension,
iv) applying an electric current to the coated device and the electrode, and
v) allowing at least some of the biologically active agent to be loaded into the voids.
15. The method of claim 14 wherein the device comprises at least a metal portion.
16. The method of claim 15 wherein the device is an expandable stent.
17. The method of claim 14 wherein the electrode functions as a cathode and the biologically active agent has a negative charge.
18. The method of claim 14 wherein the electrode functions as an anode and the biologically active agent has a positive charge.
19. The method of claim 14 wherein the polymer is an elastomer.
20. The method of claim 19 wherein the elastomer is selected from the group consisting of silicones, polyurethanes, polyisobutylene and its copolymers, thermoplastic elastomers, ethylene vinyl acetate copolymers, polyolefin elastomers, and EPDM rubbers.
21. The method of claim 14 wherein the particulate material is selected from the group consisting of polyethylene oxide, polyethylene glycol, polyethylene oxide/polypropylene oxide copolymers, polyhydroxyethylmethacrylate, polyvinylpyrrolidone, polyacrylamide and its copolymers, salts, sugars and elutable biologically active agents.
22. The method of claim 14 which further comprises curing the coating after eluting the particulate material and before loading the biologically active agent.
23. The method of claim 14 which further comprises curing the coating after it is loaded with the biologically active agent.
24. The method of claim 14 wherein at least some of the voids contain a particulate material prior to placing the device into the solution or suspension.
25. A device produced by the method of claim 1.
26. A device produced by the method of claim 14.
27. A method of making an expandable metal stent prosthesis having a surface covered with a porous coating having a plurality of voids therein to release at least one biologically active agent therefrom, the method comprising:
a) forming the porous coating on the surface by
i) applying a composition comprising a polymer and a particulate material to the surface and
ii) exposing the surface to a solvent to elute the particulate material from the polymer; and
b) loading the porous coating with the biologically active agent by
i) forming a solution or suspension of the biologically active agent,
ii) placing the coated device into the solution or suspension,
iii) placing an electrode in the solution or suspension,
iv) applying an electric current to the coated device and the electrode, and
v) allowing at least some of the biologically active agent to be loaded into the voids.
28. A method of making a stent graft having a porous surface having a plurality of voids therein to release at least one biologically active agent therefrom, the method comprising loading the porous surface with the biologically active agent by
a) forming a solution or suspension of the biologically active agent,
b) placing-the device into the solution or suspension,
c) placing an electrode in the solution or suspension,
d) applying an electric current to the device and the electrode, and
e) allowing at least some of the biologically active agent to be loaded into the voids.
Description
    FIELD OF THE INVENTION
  • [0001]
    This invention relates generally to medical devices for delivering a biologically active agent or drug to a desired location within the body of a patient. More particularly, the invention is directed to medical devices having a porous surface comprising a plurality of voids therein. The porous surface is capable of being loaded with a drug, e.g., by infusing or placing the drug into the voids, for release into the body, particularly upon expansion of the portion of the medical device with the porous surface. In one method of loading the porous surface, the drug is concentrated into the voids by electrophoresis.
  • BACKGROUND OF THE INVENTION
  • [0002]
    For certain diseases which are localized to a particular part of the body, the systemic administration of drugs for the treatment of these diseases is not preferred because of the inefficiencies associated with the indirect delivery of the drugs to the afflicted area. Also, if a drug causes significant side effects, it is generally inappropriate for systemic delivery.
  • [0003]
    Instead, it is preferred that the drug be directly applied to the diseased tissue. Because such localized delivery to the afflicted area usually requires a relatively small amount of drug, side effects of the drug are reduced. Also, since localized delivery requires smaller amounts of drugs, such delivery is desirable for expensive drugs.
  • [0004]
    However, such localized delivery of drugs to the walls of lumens, such as blood vessels and ducts, can be problematic since body lumens are generally involved in the transport of body fluids, which tend to carry the drug away from the afflicted area. Thus, there is a need for devices and methods for the localized delivery of drugs to afflicted tissue, especially body lumens.
  • [0005]
    Also, if a drug or biologically active agent is biologically derived (e.g., a gene, a protein or a lipid), it usually cannot withstand standard sterilization of the device (e.g., ETO, gamma, or e-beam sterilization, autoclaving). Thus, the number of drugs that can be incorporated into the implantable device is limited. Hence, there is a need for a method for including such drugs into a drug-releasing device.
  • [0006]
    A number of methods for delivering drugs to body lumens or vessels involve the use of catheters having expandable portions, such as a balloon, disposed on the catheter. For instance, U.S. Pat. No. 5,304,121 to Sahatjian, PCT application WO 95/03083 to Sahatjian et al. and U.S. Pat. No. 5,120,322 to Davis et al. describe medical devices in which the exterior surface of the device is coated with a swellable hydrogel polymer. A solution of a drug to be delivered to the afflicted tissue is incorporated into the hydrogel. The drug is usually pre-sterilized by such methods as filtration. The drug is held within the matrix of the hydrogel. In the case where the medical device is a balloon catheter, the drug is delivered by inserting the catheter into the body lumen and expanding the coated balloon against the afflicted tissue of the lumen to force the drug from the hydrogel into the tissue.
  • [0007]
    However, these hydrogel coated devices have certain disadvantages. In particular, because the loading of the drug into the hydrogel is based on diffusion, the amount of drug that can be loaded onto the devices is limited. Thus, there remains a need for a way to load more drug onto implantable devices.
  • [0008]
    Other methods for making a drug coated implantable device include ones in which a composition of a drug, a polymeric material and a solvent is applied to at least a surface of the device. Such a method is described in co-pending application Ser. No. 08/633,490, filed Jun. 13, 1996 and published as EP 0 822 788A2 on Feb. 11, 1998. Also, U.S. Pat. No. 5,464,650 to Berg et al. describes drug containing coatings for medical devices.
  • SUMMARY OF THE INVENTION
  • [0009]
    These and other objectives are accomplished by the present invention. To achieve the aforementioned objectives, a medical device and a method for making such device for the localized delivery of biologically active agents to a patient has been invented.
  • [0010]
    The medical devices of the invention comprise a portion which has a porous surface. The porous surface includes the pores and the material between the pores which make up the porous surface. The porous surface is made of a material, such as polymer or a polymer blend, having a plurality of voids therein. The void space of the coating is preferably greater than about 60% of the volume of the porous surface. The porous surface can be a porous coating covering the surface of the device. The thickness of such a coating can be tailored to meet individual needs for release of at least one biologically active agent. Alternatively, the porous surface can be a structural part of the device. For example, a stent graft formed of a porous membrane would have a porous surface. A biologically active agent is loaded into the voids for release when the device is implanted.
  • [0011]
    In another embodiment of the invention, the medical device is a stent endoprosthesis having at least a portion which is covered with a polymeric porous surface such as a polymeric coating or material with a plurality of voids therein. A biologically active agent or a drug is placed into the voids for controlled release when the stent is implanted or inserted into a body lumen.
  • [0012]
    In yet another embodiment, the medical device is a stent graft comprising at least one portion which is made of porous graft material, which can, but need not be further covered with a porous or “sponge” coating. A drug is loaded into the voids to form a drug-coated stent graft.
  • [0013]
    The devices of the present invention can be prepared by applying a porous coating composition to a surface of the device, e.g., stent or stent graft. The porous coating composition comprises a polymer dissolved in a solvent and an elutable particulate material. After the coating is cured, it is exposed to a solvent, e.g., water, which causes the particulate material to elute from the polymer to form a porous or sponge coating having a plurality of voids therein.
  • [0014]
    The porous surface or coating can be loaded with a drug in an electrophoresis method. In such a method, the drug is dissolved or suspended in a solvent to form a drug solution or suspension. The device and an electrode are placed into the solution or suspension. An electric current source, e.g., battery, is connected to the device and the electrode. When the current source is switched on, the drug (which has a positive or negative charge) in the solution or suspension will be loaded into the voids of the device's porous surface.
  • [0015]
    Furthermore, prior to placing the device into the drug solution or suspension, the porous surface of the device can already contain materials which do not dissolve in the solution or suspension. Such materials include drugs or radiopaque materials, which permit the device to be visible during implantation under fluoroscopy.
  • [0016]
    With certain devices which are formed of porous materials, such as a porous stent graft, such devices can be loaded without first applying a porous coating to the graft. However, a porous coating can be used in conjunction with this type of device. A device with such a porous surface can be directly loaded in an electrophoresis method as described above.
  • DESCRIPTION OF THE DRAWINGS
  • [0017]
    [0017]FIGS. 1a-1 b depict a method of preparing a porous coating for a medical device.
  • [0018]
    [0018]FIG. 2 depicts an electrophoresis method for concentrating a biologically active agent into the porous coating or material.
  • DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • [0019]
    Devices which can be used in this invention include self-expanding stents and balloon expandable stents. Examples of self-expanding stents useful in the present invention are illustrated in U.S. Pat. Nos. 4,655,771 and 4,954,126 issued to Wallsten and U.S. Pat. No. 5,061,275 issued to Wallsten et al. Examples of appropriate balloon-expandable stents are shown in U.S. Pat. No. 4,733,665 issued to Palmaz, U.S. Pat. No. 4,800,882 issued to Gianturco and U.S. Pat. No. 4,886,062 issued to Wiktor. It will be appreciated that all references cited herein are incorporated by reference in their entireties, for all purposes.
  • [0020]
    The expandable stent may be formed from polymeric, metallic, ceramic materials and/or composite materials. However, it is preferred that the stent contain a metallic material, e.g., stainless steel, nitinol, tantalum. Suitable polymeric materials include without limitation poly-L-lactic acid, polycarbonate and polyethylene terephthalate.
  • [0021]
    The stent grafts suitable for the present invention include those appropriate for cardiovascular applications, such as ones described in U.S. Pat. No. 4,657,544 to Pinchuk, or urinary applications, such as U.S. Pat. No. 4,334,327 to Lyman. Generally, such grafts are made of biocompatible polymeric materials, e.g., polyurethane, silicone, polyethylene terephthalate, teflon, or tissue engineered autografts or xenografts. As a result, when these polymeric grafts are used in the claimed electrophoresis method of the invention, it is preferable that the graft include some metallic material to conduct the current and facilitate the concentrating of the drug into the porous surface.
  • [0022]
    Furthermore, the stent graft can be formed of a porous material having a porous surface, such as a porous membrane. Examples of such stent grafts and methods for making them are described in U.S. Pat. No. 4,657,544 to Pinchuk and U.S. Pat. No. 5,758,562 to Thompson. When such porous stent grafts are used in the electrophoresis method, they can, but do not have to be coated with a porous coating before the grafts are loaded with biologically active agents.
  • [0023]
    Moreover, other implantable medical devices such as blood oxygenator, heart valves and vein valves can be used in the invention. In general, any implantable device that contains some metal portion can be used.
  • [0024]
    The following is a more detailed description of suitable materials and methods useful in producing the drug loaded coatings or materials of the invention.
  • [0025]
    The polymer(s) useful for forming the porous coating should be ones that are biostable, biocompatible, particularly during insertion or implantation of the device into the body and avoids irritation to body tissue. Examples of such polymers include without limitation polyurethanes, polyisobutylene and its copolymers, silicones, and polyesters. Other suitable polymers include polyolefins, polyisobutylene, ethylene-alphaolefin copolymers, acrylic polymers and copolymers, vinyl halide polymers and copolymers such as polyvinyl chloride, polyvinyl ethers such as polyvinyl methyl ether, polyvinylidene halides such as polyvinylidene fluoride and polyvinylidene chloride, polyacrylonitrile, polyvinyl ketones, polyvinyl aromatics such as polystyrene, polyvinyl esters such as polyvinyl acetate; copolymers of vinyl monomers, copolymers of vinyl monomers and olefins such as ethylene-methyl methacrylate copolymers, acrylonitrile-styrene copolymers, ABS resins, ethylene-vinyl acetate copolymers, polyamides such as Nylon 66 and polycaprolactone, alkyd resins, polycarbonates, polyoxyethylenes, polyimides, polyethers, epoxy resins, polyurethanes, rayon-triacetate, cellulose, cellulose acetate, cellulose butyrate, cellulose acetate butyrate, cellophane, cellulose nitrate, cellulose propionate, cellulose ethers, carboxymethyl cellulose, collagens, chitins, polylactic acid, polyglycolic acid, and polylactic acid-polyethylene oxide copolymers.
  • [0026]
    If the polymer is being applied to a part of the medical device which undergoes mechanical challenges, e.g., expansion and contraction, the polymers are preferably selected from elastomeric polymers such as silicones (e.g., polysiloxanes and substituted polysiloxanes), polyurethanes, thermoplastic elastomers, polyisobutylene and its copolymers ethylene vinyl acetate copolymers, polyolefin elastomers, and EPDM rubbers. The polymer is selected to allow the coating to better adhere to the surface of the expandable portion of the medical device when it is subjected to forces or stress.
  • [0027]
    Furthermore, although the porous or sponge coating can be formed by using a single type of polymer, various combinations of polymers can be employed. The appropriate mixture of polymers can be coordinated with biologically active agents of interest to produce desired effects when coated on a medical device in accordance with the invention.
  • [0028]
    The elutable particulate materials which can be incorporated into the polymer include without limitation polyethylene oxide, polyethylene glycol, polyethylene oxide/polypropylene oxide copolymers, polyhydroxyethyl methacrylate, polyvinylpyrrolidone, polyacrylamide and its copolymers, salts, e.g., sodium chloride, sugars, and elutable biologically active agents such as heparin.
  • [0029]
    The amount of elutable particulate material that is incorporated into the polymer should range from about 10% to 90% by weight of the porous or sponge coating and preferably, from about 30% to 70%. The average particle size of the elutable material can range from 1-100 microns and preferably from about 2 to 15 microns.
  • [0030]
    The solvent that is used to form the mixture or slurry of polymer and elutable particulate materials include ones which can dissolve the polymer into solution and do not alter or adversely impact the therapeutic properties of the material employed. Examples of useful solvents for silicone include tetrahydrofuran (THF), chloroform and dichloromethane.
  • [0031]
    The composition of polymer and elutable particulate material can be applied to a portion of the medical device in a variety of ways. For example, the composition can be spray-coated onto the device or the device can be dipped into the composition. One of skill in the art would be aware of methods for applying the coating to the device. The thickness of the porous coating can range from about 10 μm to 0.5 mm. Preferably, the thickness is about 20 μm to 100 μm.
  • [0032]
    After the composition is applied to the device, it should be cured to produce a polymer containing the particulate material and to evaporate the solvent. Certain polymers, such as silicone, can be cured at relatively low temperatures, (e.g., room temperature) in what is known as a room temperature vulcanization (RTV) process. More typically, the curing/evaporation process involves higher temperatures so that the coated device is heated in a oven. Typically, the heating occurs at approximately 90 C. or higher for approximately 1 to 16 hours when silicone is used. For certain coatings the heating may occur at temperatures as high as 150 C. The time and temperature of heating will of course vary with the particular polymer, drugs, and solvents used. One of skill in the art is aware of the necessary adjustments to these parameters.
  • [0033]
    To elute the particulate material from the polymer, a solvent is used. The device can be soaked in the solvent to elute the particulate materials. Other methods of eluting the particulate is apparent to those skilled in the art.
  • [0034]
    The choice of the solvent depends upon the solubility of the elutable particulate material in that solvent. For instance, for water-soluble particulate materials such as heparin, water can be used. For elutable particulate materials which can be dissolved in organic solvents, such organic solvents can be used. Examples of suitable solvents, without limitation, include ethanol, dimethyl sulfoxide, etc.
  • [0035]
    As shown in FIGS. 1a-1 b, in one method for forming the porous coating 100, a mixture or slurry comprising a polymer 101, an elutable particulate material 102 and a solvent is applied to a portion of the medical device. The device is then exposed to an aqueous or organic solvent to elute the particulate material 102 from the polymer 101 to form a plurality of voids 103 in the polymer 101 (FIG. 1b).
  • [0036]
    Other methods of making a porous coating/membrane are known in the art, such as several phase inversion methods. Examples of these phase inversion methods are: 1) solvent freeze drying; 2) polymer, solvent and non-solvent pore former systems; and 3) thermal processes using a latent solvent. A more detailed description of these methods can be found in R.E. Kesting “Synthetic Polymeric Membranes—A Structural Perspective”, JOHN WILEY & SONS, 2D EDITION, which is incorporated herein by reference.
  • [0037]
    After the porous coating is formed on the device, the medical device can be optionally sterilized. Depending upon the nature of the drug used, sterilization of the device can occur before or after the drug is loaded into the sponge coating. Methods of sterilization are known in the art. For example, the devices can be sterilized by exposure to gamma radiation at 2.5-3.5 Mrad or by exposure to ethylene oxide.
  • [0038]
    The porous materials or membranes which can be used to form porous stent graft can be made of a polymer. Suitable polymers include polyurethane, silicone, polytetra fluorethylene, polyethylene terephthalate, polyisobutylene and its copolymers, polylactic acid, polyglycolic acid and its copolymers, cellulose and its derivatives. Graft materials can also be biologically derived. For example, collagen, elastin, tissue engineered autografts or xenografts are suitable.
  • [0039]
    As noted early, it is desirable that the stent graft contain some metallic material to facilitate loading of the coating with a drug by electrophoresis. Such metallic material can be incorporated by laminating or cladding a metal or an metallic alloy onto the porous graft material.
  • [0040]
    To load the biologically active agent in the porous surface, an electrophoresis method can be used. Specifically, as described in FIG. 2, a graft or other medical device 10 having a porous surface 11 containing voids 12 is placed into a container 15 which holds a solution or a suspension 13 of a drug 14. The drug 14 does not have to be dissolved in a solvent. It can remain as a suspension such as a slurry.
  • [0041]
    Also placed in the container 15 is an electrode 16, typically made of metal. The electrode 16 and the device 10 with the porous surface 11 are connected, typically by wires 17 to a current source 18, such as a battery. When the current source 18 is switched on, at least some of the drug 14, which contains either a positive or negative charge, is loaded into the voids 12, thereby increasing the amount of the drug at the porous surface. In other words, when an electric field is applied to the solution containing the drug, the charged drug molecules are forced to move toward the electrode with the opposite charge. Depending upon the charge on the drug 14, the device 10 functions as either an anode or cathode. If the drug 14 is negatively charged, e.g., a protein or heparin, the device 10 will function as an anode. If the drug 14 is positively charged, the device 10 will function as a cathode.
  • [0042]
    Also, the type of electrode 16, i.e., its material, used will depend upon whether the device 10 functions as an anode or cathode. For example, if the device 10 is an anode, an electrode 16 which can function as a cathode is used. Persons skilled in the art are aware of how to select suitable electrodes 16.
  • [0043]
    Furthermore, by adjusting the pH of the drug solution or suspension 13, the mobility of the drug 14 under the electric current can be varied. Specifically, at different pH levels, the predominant ionic form of the drug 14 will be different. For example, with respect to amino acids, if the pH of the solution or suspension 13 is low, e.g., acidic, the carboxyl group is un-ionized and the amino group is ionized. When amino acids are placed into a solution or suspension 13 with a high pH level, the carboxyl group is ionized and the amino group is un-ionized. Such changes in the ionic form or charge form of the drug 14 affects its mobility under the electric current.
  • [0044]
    It should be noted that the porous surface of the device can contain some biologically active agent even before the surface is loaded with the drug 14 according to this method. More specifically, prior to placing the devices into the drug solution or suspension 13 the porous surface may already contain materials, such as particulate materials, that provide desirable properties to the device. These materials should not be soluble or elutable in the solvent forming the drug solution or suspension 13. They can include another biologically active agent or radiopaque materials to allow the device to be visible during implantation under fluoroscopy.
  • [0045]
    As used herein, “biologically active agent” or “drug” refers not only to the molecular or charged form of the biologically active agent or drug but also to formulations containing the same, such as, without limitation, liposomes, emulsions with surfactant and cyclodextrin encapsulations.
  • [0046]
    Preferably, biologically active agents having an electric charge are used in this invention. However, a neutral or a weakly charged biologically active agent can also be used if it can be converted to a charged moiety. There are a variety of ways for carrying out such a conversion. For instance, one typical method includes forming an emulsion of the drug or drug particle with a surfactant. Examples of surfactants which can be used are, without limitation, fatty acids, phospholipids and sodium cetyl sulfate. In another method, the biologically active agent can be converted to a charged moiety by cyclodextrin encapsulation.
  • [0047]
    Suitable biologically active agents that can be used in this invention include without limitation glucocorticoids (e.g., dexamethasone, betamethasone), heparin, hirudin, angiopeptin, aspirin, growth factors, oligonucleotides, and, more generally, antiplatelet agents, anti-coagulant agents, antimitotic agents, antioxidants, antimetabolite agents, anti-cancer agents and anti-inflammatory agents could be used. Antiplatelet agents can include drugs such as aspirin. Aspirin is classified as an analgesic, antipyretic, anti-inflammatory and antiplatelet drug. Anticoagulant agents can include drugs such as glycosaminoglycan, protamine, hirudin and tick anticoagulant protein. Glycosaminoglycans include heparin, heparin sulfate, hyaluronic acid, chondroitin, chondroitin sulfate, dermatan sulfate and keratosulfate and their respective derivatives. Antimitotic agents and antimetabolite agents can include drugs such as methotrexate. Antibiotic agents can include penicillin, cefoxitin, and oxacillin. Also, genes or nucleic acids, or portions thereof can be used. Such genes or nucleic acids can first be packaged in liposomes or nanoparticles. Furthermore, collagen synthesis inhibitors, such as tranilast, can be used.
  • [0048]
    The description contained herein is for purposes of illustration and not for purposes of limitation. Changes and modifications may be made to the embodiments of the description and still be within the scope of the invention. Furthermore, obvious changes, modifications or variations will occur to those skilled in the art. Also, all references cited above are incorporated herein, in their entirety, for all purposes related to this disclosure.
Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US3758396 *Aug 31, 1971Sep 11, 1973Research CorpItion preparation of immobilized enzymemembrane complexes by electrocodepos
US4101984 *May 5, 1976Jul 25, 1978Macgregor David CCardiovascular prosthetic devices and implants with porous systems
US4334327 *Dec 21, 1979Jun 15, 1982University Of UtahUreteral prosthesis
US4655771 *Apr 11, 1983Apr 7, 1987Shepherd Patents S.A.Prosthesis comprising an expansible or contractile tubular body
US4657544 *Apr 18, 1984Apr 14, 1987Cordis CorporationCardiovascular graft and method of forming same
US4733665 *Nov 7, 1985Mar 29, 1988Expandable Grafts PartnershipExpandable intraluminal graft, and method and apparatus for implanting an expandable intraluminal graft
US4800882 *Mar 13, 1987Jan 31, 1989Cook IncorporatedEndovascular stent and delivery system
US4886062 *Oct 19, 1987Dec 12, 1989Medtronic, Inc.Intravascular radially expandable stent and method of implant
US4954126 *Mar 28, 1989Sep 4, 1990Shepherd Patents S.A.Prosthesis comprising an expansible or contractile tubular body
US5061275 *Dec 29, 1989Oct 29, 1991Medinvent S.A.Self-expanding prosthesis
US5120322 *Jun 13, 1990Jun 9, 1992Lathrotec, Inc.Method and apparatus for treatment of fibrotic lesions
US5147370 *Jun 12, 1991Sep 15, 1992Mcnamara Thomas ONitinol stent for hollow body conduits
US5205921 *Feb 4, 1991Apr 27, 1993Queen's University At KingstonMethod for depositing bioactive coatings on conductive substrates
US5304121 *Nov 22, 1991Apr 19, 1994Boston Scientific CorporationDrug delivery system making use of a hydrogel polymer coating
US5464650 *Apr 26, 1993Nov 7, 1995Medtronic, Inc.Intravascular stent and method
US5693085 *Apr 26, 1995Dec 2, 1997Scimed Life Systems, Inc.Stent with collagen
US5758562 *Apr 30, 1996Jun 2, 1998Schneider (Usa) Inc.Process for manufacturing braided composite prosthesis
US5843172 *Apr 15, 1997Dec 1, 1998Advanced Cardiovascular Systems, Inc.Porous medicated stent
US5972027 *Sep 30, 1997Oct 26, 1999Scimed Life Systems, IncPorous stent drug delivery system
US6391052 *Oct 29, 1997May 21, 2002Scimed Life Systems, Inc.Stent with collagen
US6635082 *Dec 29, 2000Oct 21, 2003Advanced Cardiovascular Systems Inc.Radiopaque stent
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US7582068Feb 18, 2004Sep 1, 2009Medtronic, Inc.Occlusion resistant hydrocephalic shunt
US7862835Oct 27, 2004Jan 4, 2011Boston Scientific Scimed, Inc.Method of manufacturing a medical device having a porous coating thereon
US7931683Jul 27, 2007Apr 26, 2011Boston Scientific Scimed, Inc.Articles having ceramic coated surfaces
US7938855May 10, 2011Boston Scientific Scimed, Inc.Deformable underlayer for stent
US7942926Jul 11, 2007May 17, 2011Boston Scientific Scimed, Inc.Endoprosthesis coating
US7964209Jun 21, 2011Boston Scientific Scimed, Inc.Orienting polymer domains for controlled drug delivery
US7976915Jul 12, 2011Boston Scientific Scimed, Inc.Endoprosthesis with select ceramic morphology
US7981150Jul 19, 2011Boston Scientific Scimed, Inc.Endoprosthesis with coatings
US7985252Jul 30, 2008Jul 26, 2011Boston Scientific Scimed, Inc.Bioerodible endoprosthesis
US7998192Aug 16, 2011Boston Scientific Scimed, Inc.Endoprostheses
US8002821Aug 23, 2011Boston Scientific Scimed, Inc.Bioerodible metallic ENDOPROSTHESES
US8002823Jul 11, 2007Aug 23, 2011Boston Scientific Scimed, Inc.Endoprosthesis coating
US8029554Nov 2, 2007Oct 4, 2011Boston Scientific Scimed, Inc.Stent with embedded material
US8048150Apr 12, 2006Nov 1, 2011Boston Scientific Scimed, Inc.Endoprosthesis having a fiber meshwork disposed thereon
US8052743Aug 2, 2007Nov 8, 2011Boston Scientific Scimed, Inc.Endoprosthesis with three-dimensional disintegration control
US8052744Sep 13, 2007Nov 8, 2011Boston Scientific Scimed, Inc.Medical devices and methods of making the same
US8052745Nov 8, 2011Boston Scientific Scimed, Inc.Endoprosthesis
US8057534Sep 14, 2007Nov 15, 2011Boston Scientific Scimed, Inc.Bioerodible endoprostheses and methods of making the same
US8066763May 11, 2010Nov 29, 2011Boston Scientific Scimed, Inc.Drug-releasing stent with ceramic-containing layer
US8067054Nov 29, 2011Boston Scientific Scimed, Inc.Stents with ceramic drug reservoir layer and methods of making and using the same
US8070797Dec 6, 2011Boston Scientific Scimed, Inc.Medical device with a porous surface for delivery of a therapeutic agent
US8071156Mar 4, 2009Dec 6, 2011Boston Scientific Scimed, Inc.Endoprostheses
US8080055Dec 20, 2011Boston Scientific Scimed, Inc.Bioerodible endoprostheses and methods of making the same
US8089029Feb 1, 2006Jan 3, 2012Boston Scientific Scimed, Inc.Bioabsorbable metal medical device and method of manufacture
US8114427Oct 18, 2005Feb 14, 2012Gerhard SchmidmaierBiologically active implants
US8128689Sep 14, 2007Mar 6, 2012Boston Scientific Scimed, Inc.Bioerodible endoprosthesis with biostable inorganic layers
US8187620May 29, 2012Boston Scientific Scimed, Inc.Medical devices comprising a porous metal oxide or metal material and a polymer coating for delivering therapeutic agents
US8216632Jul 10, 2012Boston Scientific Scimed, Inc.Endoprosthesis coating
US8221822Jul 30, 2008Jul 17, 2012Boston Scientific Scimed, Inc.Medical device coating by laser cladding
US8231980Jul 31, 2012Boston Scientific Scimed, Inc.Medical implants including iridium oxide
US8236046Jun 10, 2008Aug 7, 2012Boston Scientific Scimed, Inc.Bioerodible endoprosthesis
US8267992Sep 18, 2012Boston Scientific Scimed, Inc.Self-buffering medical implants
US8287937Apr 24, 2009Oct 16, 2012Boston Scientific Scimed, Inc.Endoprosthese
US8303643Nov 6, 2012Remon Medical Technologies Ltd.Method and device for electrochemical formation of therapeutic species in vivo
US8353949Sep 10, 2007Jan 15, 2013Boston Scientific Scimed, Inc.Medical devices with drug-eluting coating
US8382824Oct 3, 2008Feb 26, 2013Boston Scientific Scimed, Inc.Medical implant having NANO-crystal grains with barrier layers of metal nitrides or fluorides
US8431149Apr 30, 2013Boston Scientific Scimed, Inc.Coated medical devices for abluminal drug delivery
US8449603May 28, 2013Boston Scientific Scimed, Inc.Endoprosthesis coating
US8513353Mar 19, 2009Aug 20, 2013Agency For Science, Technology And ResearchForming copolymer from bicontinuous microemulsion comprising monomers of different hydrophilicity
US8574615May 25, 2010Nov 5, 2013Boston Scientific Scimed, Inc.Medical devices having nanoporous coatings for controlled therapeutic agent delivery
US8668732Mar 22, 2011Mar 11, 2014Boston Scientific Scimed, Inc.Surface treated bioerodible metal endoprostheses
US8715339Nov 21, 2011May 6, 2014Boston Scientific Scimed, Inc.Bioerodible endoprostheses and methods of making the same
US8771343Jun 15, 2007Jul 8, 2014Boston Scientific Scimed, Inc.Medical devices with selective titanium oxide coatings
US8808726Sep 14, 2007Aug 19, 2014Boston Scientific Scimed. Inc.Bioerodible endoprostheses and methods of making the same
US8815273Jul 27, 2007Aug 26, 2014Boston Scientific Scimed, Inc.Drug eluting medical devices having porous layers
US8815275Jun 28, 2006Aug 26, 2014Boston Scientific Scimed, Inc.Coatings for medical devices comprising a therapeutic agent and a metallic material
US8840660Jan 5, 2006Sep 23, 2014Boston Scientific Scimed, Inc.Bioerodible endoprostheses and methods of making the same
US8900292Oct 6, 2009Dec 2, 2014Boston Scientific Scimed, Inc.Coating for medical device having increased surface area
US8920491Apr 17, 2009Dec 30, 2014Boston Scientific Scimed, Inc.Medical devices having a coating of inorganic material
US8932346Apr 23, 2009Jan 13, 2015Boston Scientific Scimed, Inc.Medical devices having inorganic particle layers
US9284409Jul 17, 2008Mar 15, 2016Boston Scientific Scimed, Inc.Endoprosthesis having a non-fouling surface
US20050079199 *Sep 3, 2004Apr 14, 2005Medtronic, Inc.Porous coatings for drug release from medical devices
US20060039947 *Oct 18, 2005Feb 23, 2006Gerhard SchmidmaierBiologically active implants
US20060051392 *Sep 3, 2004Mar 9, 2006Medtronic, Inc.Porous coatings for drug release from medical devices
US20060051393 *Sep 8, 2004Mar 9, 2006Medtronic, Inc.Method of manufacturing drug-eluting medical device
US20060088567 *Oct 27, 2004Apr 27, 2006Scimed Life SystemsMethod of manufacturing a medical device having a porous coating thereon
US20070154522 *Aug 4, 2004Jul 5, 2007Chow Edwin P YPolymer having interconnected pores for drug delivery and method
US20080251391 *Apr 10, 2008Oct 16, 2008Boston Scientific Scimed, Inc.Methods and systems for applying therapeutic agent to a medical device
US20090317538 *Dec 24, 2009Gerhard SchmidmaierBiologically active implants
US20100048755 *Nov 17, 2007Feb 25, 2010Edwin Pei Yong ChowPorous polymeric material with cross-linkable wetting agent
CN103757683A *Jan 7, 2014Apr 30, 2014江南大学Electrodeposition preparation method of light-crosslinking bio-based coating
EP1475110A1 *May 10, 2004Nov 10, 2004B. Braun Melsungen AgStent for controlled drug release
WO2006029301A2 *Sep 8, 2005Mar 16, 2006Medtronic, Inc.Method of manufacturing drug-eluting medical device
WO2006029301A3 *Sep 8, 2005Aug 24, 2006Medtronic IncMethod of manufacturing drug-eluting medical device
WO2006049943A2Oct 25, 2005May 11, 2006Boston Scientific Scimed, Inc.Method of manufacturing a medical device having a porous coating thereon
WO2006049943A3 *Oct 25, 2005Sep 14, 2006Michael ArneyMethod of manufacturing a medical device having a porous coating thereon
WO2006062975A2 *Dec 7, 2005Jun 15, 2006Boston Scientific Scimed, Inc.Orienting polymer domains for controlled drug delivery
WO2006062975A3 *Dec 7, 2005Jan 11, 2007Boston Scient Scimed IncOrienting polymer domains for controlled drug delivery
WO2008127964A3 *Apr 10, 2008Dec 10, 2009Boston Scientific Scimed, Inc.Methods and systems for applying therapeutic agent to a medical device
Classifications
U.S. Classification427/2.25, 204/551
International ClassificationA61F2/82, A61F2/00, A61L31/14, A61L31/10, A61L31/16, A61L31/00
Cooperative ClassificationA61F2/07, A61L31/16, A61F2250/0067, A61L31/10, A61L2300/42, A61F2/82, A61L2300/236, A61L31/146
European ClassificationA61F2/82, A61L31/10, A61L31/16, A61L31/14H
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Owner name: BOSTON SCIENTIFIC SCIMED, INC., MINNESOTA
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Effective date: 20041222
Owner name: BOSTON SCIENTIFIC SCIMED, INC., MINNESOTA
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Effective date: 19990427