Method of providing a substrate with a hydrophilic coating and substrates, particularly medical devices, provided with such coatings

• US 5,702,754 A
• Filed: 02/22/1995
• Issued: 12/30/1997
• Est. Priority Date: 02/22/1995
• Status: Expired due to Term

• Current Assignee: Boston Scientific Scimed, Inc. (Boston Scientific Corporation)
• Original Assignee: Meadox Medicals, Inc. (Boston Scientific Corporation)
• Inventors: Zhong, Sheng-Ping
• Primary Examiner(s): DUDASH, DIANA L
• Application Number:
  US08/392,141
• Time in Patent Office: 1,042 Days
• Field of Search: 427/2.3, 427/2.28, 427/302, 427/333, 427/340, 427/2.12
• US Class Current: 427/2.12
• CPC Class Codes: A61L 2300/21 Acids
• CPC Class Codes: A61L 2300/608 having two or more layers
• CPC Class Codes: A61L 2420/08 Coatings comprising two or more layers
• 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 31/16 Biologically active materials, e.g. therapeutic substances A61L31/047 takes precedence
• CPC Class Codes: C08L 75/04 Polyurethanes
• CPC Class Codes: Y10T 428/31565 Next to polyester [polyethylene terephthalate, etc.]
• CPC Class Codes: Y10T 428/31573 Next to addition polymer of ethylenically unsaturated monomer
• CPC Class Codes: Y10T 428/31576 Ester monomer type [polyvinylacetate, etc.]
• CPC Class Codes: Y10T 428/3158 Halide monomer type [polyvinyl chloride, etc.]

Abstract

A substrate such as a catheter or a guide wire is provided with a lubricous, hydrophilic abrasion-resistant coating by:

a) coating said substrate with a first aqueous coating composition comprising an aqueous dispersion or emulsion of a polymer having organic acid functional groups and a polyfunctional crosslinking agent having functional groups capable of reacting with organic acid groups, and drying the coating to obtain a substantially water-insoluble coating layer having excess polyfunctional including functional groups being reactive with organic acid groups remaining, and

b) contacting the dried coating layer obtained in a) with a second aqueous coating composition comprising an aqueous solution or dispersion of a hydrophilic polymer having organic acid functional groups, and drying the combined coating, the hydrophilic polymer thereby becoming bonded to the polymer of the first coating composition through the excess crosslinking agent.

The drying can be carried out at ambient (room) temperature.

Claims

1. A method of providing a substrate, with a hydrophilic coating which becomes lubricous when contacted with an aqueous fluid, said method comprising:

a) coating said substrate with a first aqueous coating composition comprising an aqueous dispersion or emulsion of a polymer having organic acid functional groups and an excess of a polyfunctional cross-linking agent having functional groups being capable of reacting with organic acid groups, and drying said first coating composition to obtain a substantially water-insoluble coating layer still including functional groups being reactive with organic acid groups, and

b) forming a continuous lubricious surface over said first coating composition by contacting said dried first coating composition with a second aqueous coating composition comprising an aqueous solution or dispersion of a hydrophilic polymer having organic acid functional groups, and drying the combined coatings, to bond the hydrophilic polymer to the polymer of the first coating composition through said excess cross-linking agent.

2. A method according to claim 1, wherein the hydrophilic polymer becomes bonded to the polymer of the first coating composition through covalent bonding.

3. A method according to claim 1, wherein the organic acid functional groups are selected from free carboxylic or sulfonic acid groups, metal salts of such acid groups, including alkali metal salts, and quaternary amine salts of such acid groups.

4. A method according to claim 1, wherein the polyfunctional crosslinking agent is selected from polyfunctional aziridines, polyfunctional carboimides and combinations thereof.

5. A method according to claim 1, wherein the polyfunctional crosslinking agent is a crosslinking agent having more than two functional groups per molecule.

6. A method according to claim 1, wherein the polymer in the first coating composition is selected from homo- and copolymers having organic acid functional groups in their structure in an amount sufficient to react with said polyfunctional cross-linking agent.

7. A method according to claim 1, wherein the polymer in the first coating composition is selected from the group consisting of polyurethanes, polyacrylates, polymethacrylates, polyisocrotonates, epoxy resins, acrylate-urethane copolymers and combinations thereof.

8. A method according to claim 7, wherein the polymer in the first coating composition is an acrylate-urethane copolymer and/or a polyurethane.

9. A method according to claim 1, wherein the hydrophilic polymer comprises monomer units from at least one monomer having organic acid functional groups.

10. A method according to claim 9, wherein the hydrophillic polymer is selected from the group consisting of copolymers of acrylic acid, methacrylic acid, isocrotonic acid and combinations thereof.

11. A method according to claim 9, wherein said hydrophilic polymer is formed from monomer units without any organic acid functional groups.

12. A method according to claim 9, wherein the hydrophilic polymer comprises an acrylamide-acrylic acid copolymer.

13. A method according to claim 1, wherein the hydrophilic polymer in the second coating composition has a molecular weight in the range from about 100,000 to about 15 million.

14. A method according to claim 13, wherein the hydrophilic polymer in the second coating composition has a molecular weight in the range of from about 150,000 to about 10 million.

15. A method according to claim 14, wherein the hydrophilic polymer in the second coating composition has a molecular weight in the range of from about 400,000 to about 10 million.

16. A method according to claim 1, wherein the concentration of the hydrophilic polymer in the second coating composition is from about 0.1 to about 5% by weight solids content.

17. A method according to claim 16, wherein the concentration of the hydrophilic polymer in the second coating composition is from about 0.5 to about 3% by weight solids content.

18. A method according to claim 1, wherein the concentration of the polymer in the first coating composition is from about 2 to about 60% by weight solids content.

19. A method according to claim 1, wherein the concentration of the polymer in the first coating composition is from about 5 to about 40% by weight solids content.

20. A method according to claim 1, wherein the concentration of the crosslinking agent in the first coating composition is in the range from about 0.2 to about 30% by weight.

21. A method according to claim 1, wherein the functional groups of the crosslinking agent react with the organic acid functional groups of the polymer in the first coating composition and the hydrophilic polymer in the second coating composition at a temperature below 120°

C.

22. A method according to claim 21, wherein the functional groups of the crosslinking agent react with the organic acid functional groups of the polymer in the first coating composition and the hydrophilic polymer in the second coating composition at a temperature in a range of 10°

-70°

C.

23. The method of claim 1, wherein the substrate is a medical device.

24. The method of claim 1, wherein the substrate is an implantable medical device.

25. The method of claim 1, wherein the substrate is a catheter.

26. The method of claim 1, wherein the substrate is an angioplasty balloon catheter.

27. The method of claim 1, wherein the substrate is a biopsy catheter.