Implantable device having a coating comprising carrageenan and a biostable polymer

• US 8,703,169 B1
• Filed: 08/08/2007
• Issued: 04/22/2014
• Est. Priority Date: 08/15/2006
• Status: Expired due to Fees

• Current Assignee: Abbott Cardiovascular Systems Incorporated (Abbott Laboratories)
• Original Assignee: Abbott Cardiovascular Systems Incorporated (Abbott Laboratories)
• Inventors: Lee, Jeong
• Primary Examiner(s): Heyer, Dennis
• Application Number:
  US11/891,150
• Time in Patent Office: 2,449 Days
• Field of Search: None
• US Class Current: 424/426
• CPC Class Codes: A61F 2/82 Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents stent-grafts for tubular structures of the body other than blood vessels A61F2/04; stent-grafts for blood vessels A61F2/07; instruments specially adapted for placement or removal of stents or stent-grafts A61F2/95; for closing wounds, or holding wounds closed A61B17/04 - A61B17/115; dilators A61M29/00
• CPC Class Codes: A61F 2250/0067 Means for introducing or releasing pharmaceutical products into the body
• CPC Class Codes: A61K 31/00 Medicinal preparations containing organic active ingredients
• CPC Class Codes: A61L 2300/114 Nitric oxide, i.e. NO
• CPC Class Codes: A61L 2300/416 Anti-neoplastic or anti-proliferative or anti-restenosis or anti-angiogenic agents, e.g. paclitaxel, sirolimus
• CPC Class Codes: A61L 2300/43 Hormones, e.g. dexamethasone
• CPC Class Codes: A61L 2300/604 Biodegradation
• CPC Class Codes: A61L 2300/606 Coatings
• CPC Class Codes: A61L 31/10 Macromolecular materials
• CPC Class Codes: A61L 31/148 Materials at least partially resorbable by the body
• CPC Class Codes: A61L 31/16 Biologically active materials, e.g. therapeutic substances A61L31/047 takes precedence
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• CPC Class Codes: C08L 5/00 Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00

Abstract

The present invention provides an implantable device having a coating including a slow dissolving polymer or material and the methods of making and using the same.

Claims

1. An implantable device, comprising a polymeric matrix, said matrix disposed over essentially the entire exposed surface of the implantable device, said matrix consisting of a water dissolvable polymer or material, a biostable polymer, and one or more bioactive agents;

the water dissolvable polymer or material being selected from the group consisting of kappa carrageenan, iota carrageenan, and lambda carrageenan; and

the biostable polymer being selected from the group consisting of polyethers, polyolefins, polyisobutylene and ethylene-alphaolefin copolymers, vinyl halide polymers and copolymers, polyvinyl chloride, polyvinyl ethers, polyvinyl methyl ether, polyvinylidene chloride, polyvinyl ketones, polyvinyl alcohol, polyvinyl acetate, acrylonitrile-styrene copolymers, ABS resins, ethylene-vinyl acetate copolymers, polyamides, Nylon 66, co-polyamides, poly ether or ester block amide, polyoxymethylenes, polyimides, poly(propylene fumarate), poly(n-butyl methacrylate), poly(sec-butyl methacrylate), poly(isobutyl methacrylate), poly(tert-butyl methacrylate), poly(n-propyl methacrylate), poly(isopropyl methacrylate), poly(ethyl methacrylate), poly(methyl methacrylate), epoxy resins, polyurethanes, rayon, rayon-triacetate, polyethers, poly(ethylene glycol), polyalkylene oxides, poly(ethylene oxide), poly(propylene oxide), polymers and co-polymers of choline or phosphoryl choline bearing monomers, polymers and co-polymers of hydroxyl bearing monomers, 2-hydroxyethyl methacrylate, hydroxypropyl methacrylate, hydroxypropyl methacrylamide, poly(ethylene glycol)-acrylate, poly(ethylene glycol)-methacrylate, copolymers and polymers of 2-methacryloyloxyethylphosphorylcholine and n-vinyl pyrrolidone, alkoxymethacrylate, alkoxyacrylate, 3-trimethylsilylpropyl methacrylate, poly(styrene-isoprene-styrene)-poly(ethylene glycol), polystyrene-poly(ethylene glycol), polyisobutylene-poly(ethylene glycol), poly(methyl methacrylate)-poly(ethylene glycol), polydimethylsiloxane-co-poly(ethylene glycol), polypropylene oxide-co-polyethylene glycol surfactants, poly(tetramethylene glycol), and hydroxy functional poly(vinyl pyrrolidone).

2. The implantable device of claim 1, wherein the water dissolvable polymer is iota carrageenan.

3. The implantable device of claim 1, wherein the water dissolvable polymer is kappa carrageenan.

4. The implantable device of claim 1, wherein the bioactive agent is selected from the group consisting of paclitaxel, docetaxel, estradiol, 17-beta-estradiol, nitric oxide donors, super oxide dismutases, 4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl (4-amino-TEMPO), biolimus, tacrolimus, dexamethasone, rapamycin, everolimus, 40-O-(3-hydroxy)propyl-rapamycin, 40-O-[2-(2 hydroxy)ethoxy]ethyl-rapamycin, 40-O-tetrazole-rapamycin, 40-epi-(N1-tetrazolyl)-rapamycin (ABT-578), γ

-hiridun, clobetasol, pimecrolimus, imatinib mesylate, midostaurin, and combinations thereof.

5. The implantable device of claim 1, which is a stent.

6. The implantable device of claim 4, which is a stent.

7. The implantable device of claim 1, wherein the water dissolvable polymer is lambda carrageenan.

8. The implantable medical device of claim 1, wherein the water dissolvable polymer or material will completely dissolve into a physiological environment upon implantation over a period from about 1 day to about 2 years.

9. A method, comprising implanting in a patient the implantable device according to claim 6, to treat, mitigate, and/or reduce a disorder, wherein the disorder is selected from the group consisting of atherosclerosis, thrombosis, restenosis, hemorrhage, vascular dissection or perforation, vascular aneurysm, vulnerable plaque, chronic total occlusion, patent foramen ovale, claudication, anastomotic proliferation for vein and artificial grafts, bile duct obstruction, ureter obstruction tumor obstruction, and combinations thereof.

10. The implantable device of claim 1, wherein the biostable polymer of the polymeric matrix is selected from the group consisting of polyvinyl chloride, polyvinyl methyl ether, polyvinylidene chloride, polyvinyl alcohol, polyvinyl acetate, acrylonitrile-styrene copolymers, ABS resins, ethylene-vinyl acetate copolymers, Nylon 66, poly(propylene fumarate), poly(n-butyl methacrylate), poly(sec-butyl methacrylate), poly(isobutyl methacrylate), poly(tert-butyl methacrylate), poly(n-propyl methacrylate), poly(isopropyl methacrylate), poly(ethyl methacrylate), poly(methyl methacrylate), rayon, rayon-triacetate, poly(ethylene glycol), poly(ethylene oxide), poly(propylene oxide), poly(styrene-isoprene-styrene)-poly(ethylene glycol), polystyrene-poly(ethylene glycol), polyisobutylene-poly(ethylene glycol), poly(methyl methacrylate)-poly(ethylene glycol), polydimethylsiloxane-co-poly(ethylene glycol), polypropylene oxide-co-polyethylene glycol surfactants, and poly(tetramethylene glycol).