Drug-releasing coatings for medical devices

• US 5,879,697 A
• Filed: 04/30/1997
• Issued: 03/09/1999
• Est. Priority Date: 04/30/1997
• Status: Expired due to Term

• Current Assignee: Boston Scientific Scimed (Boston Scientific Corporation)
• Original Assignee: Boston Scientific Scimed (Boston Scientific Corporation)
• Inventors: Ding, Ni, Raeder-Devens, Jennifer E., Trinh, Tuyethoa Thi
• Primary Examiner(s): Brouillette, D. Gabrielle
• Application Number:
  US08/841,747
• Time in Patent Office: 678 Days
• Field of Search: 424/422, 424/423, 424/424, 604/891.1, 623/11
• US Class Current: 424/422
• CPC Class Codes: A61L 2300/236 Glycosaminoglycans, e.g. heparin, hyaluronic acid, chondroitin
• CPC Class Codes: A61L 2300/258 Genetic materials, DNA, RNA, genes, vectors, e.g. plasmids
• CPC Class Codes: A61L 2300/41 Anti-inflammatory agents, e.g. NSAIDs
• CPC Class Codes: A61L 2300/414 Growth factors
• CPC Class Codes: A61L 2300/42 Anti-thrombotic agents, anticoagulants, anti-platelet agents
• CPC Class Codes: A61L 2300/602 Type of release, e.g. controlled, sustained, slow
• CPC Class Codes: A61L 2300/606 Coatings
• CPC Class Codes: A61L 2300/608 having two or more layers
• CPC Class Codes: A61L 2300/61 containing two or more active agents in different layers
• CPC Class Codes: A61L 2300/802 Additives, excipients, e.g. cyclodextrins, fatty acids, surfactants
• CPC Class Codes: A61L 27/34 Macromolecular materials
• CPC Class Codes: A61L 27/50 Materials characterised by their function or physical properties , e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
• CPC Class Codes: A61L 29/085 Macromolecular materials
• CPC Class Codes: A61L 29/16 Biologically active materials, e.g. therapeutic substances A61L29/048 takes precedence
• CPC Class Codes: A61L 31/10 Macromolecular materials
• CPC Class Codes: A61L 31/16 Biologically active materials, e.g. therapeutic substances A61L31/047 takes precedence

Abstract

The invention is directed to medical devices having a drug-releasing coating and methods for making such coated devices. The coating permits timed or prolonged pharmacological activity on the surface of medical devices through a reservoir concept. Specifically, the coating comprises at least two layers: an outer layer containing at least one drug-ionic surfactant complex overlying a reservoir layer containing a polymer and the drug which is substantially free of an ionic surfactant. Upon exposure to body tissue of a medical device covered with such coating, the ionically bound drug in the outer layer is released into body fluid or tissue. Following release of such bound drug, the ionic surfactant binding sites in the outer layer are left vacant. To maintain the pharmacological activity after delivery of the ionically bound drug, additional amounts of the drug are embedded or incorporated in the reservoir layer in a manner which allows the drug, which is substantially free of ionic surfactants, to complex with the vacant binding sites of the ionic surfactant of the outer layer. As a result, the surface of the medical device is enriched with the drug to provide sustained pharmacological activity to prevent the adverse reaction due to the presence of the medical device. The invention is further directed to medical devices with stabilized drug-releasing coatings. The coatings are stabilized by exposure to a low energy, relatively non-penetrating energy source, e.g., gas plasma or an electron beam energy source.

Claims

1. A medical device having at least a portion which is insertable or implantable 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 coating for release of at least one biologically active material, the coating comprising an internal reservoir layer and an outer layer in contact with the reservoir layer;

wherein the outer layer comprises an ionic surfactant complexed to the biologically active material; and

wherein the reservoir layer comprises a polymer incorporating the biologically active material which is substantially free of any ionic surfactant such that the biologically active material of the reservoir layer can migrate outwardly from the reservoir layer, and at least some of the biologically active material of the reservoir can complex with the ionic surfactant in the outer layer as the biologically active material releases from the outer layer.

2. The device of claim 1 wherein the device is an expandable stent.

3. The device of claim 2 wherein the device is a self-expanding stent.

4. The device of claim 1 wherein the polymer of the reservoir layer is an elastomeric material.

5. The device of claim 4 wherein the polymer of the reservoir layer is selected from the group consisting of silicones, polyurethanes, thermoplastic elastomers, ethylene vinyl acetate copolymers, polyolefin elastomers, and EPDM rubbers.

6. The device of claim 5 wherein the polymer of the reservoir layer is silicone.

7. The device of claim 1 wherein the biologically active material of the reservoir layer is in a particulate form having an average particle size of 1 to 100 microns.

8. The device of claim 7 wherein the ratio of reservoir layer thickness to average particle diameter is greater than about 3.

9. The device of claim 7 wherein the ratio of reservoir layer thickness to average particle diameter is greater than about 5.

10. The device of claim 1 wherein the biologically active material is selected from the group consisting of glucocorticoids, heparin, hirudin, angiopeptin, aspirin, ACE inhibitors, growth factors, oligonucleotides, antiplatelet agents, anti-hypertensives, anti-coagulant agents, antimitotic agents, antioxidants, antimetabolite agents, anti-inflammatory agents and antibiotics.

11. The device of claim 10 wherein the biologically active material is heparin.

12. The device of claim 1 wherein the reservoir layer comprises about 0.1 to about 90 weight % of the biologically active material.

13. The device of claim 12 wherein the reservoir layer comprises about 10 to about 45 weight % of the biologically active material.

14. The device of claim 1 wherein the reservoir layer is about 5 to about 200 microns thick.

15. The device of claim 14 wherein the reservoir layer is about 15 to about 50 microns thick.

16. The device of claim 1 wherein the ionic surfactant of the outer layer is a quaternary ammonium complex.

17. The device of claim 16 wherein the ionic surfactant comprises a tridodecylmethylammonium ion.

18. The device of claim 1 wherein the outer layer is about 0.1 to about 10 microns thick.

19. The device of claim 1 wherein the coating is constructed to maintain biologically active material on the surface of the device for at least about 24 hours.