Water insoluble derivatives of hyaluronic acid

• US 4,937,270 A
• Filed: 09/18/1987
• Issued: 06/26/1990
• Est. Priority Date: 09/18/1987
• Status: Expired due to Term

• Current Assignee: Genzyme Corporation (Sanofi )
• Original Assignee: Genzyme Corporation (Sanofi )
• Inventors: Acharya, Raksha A., Hamilton, Raymond, Walts, Alan E., Fox, Ellen M.
• Primary Examiner(s): Bell, Mark L.
• Assistant Examiner(s): Brunsman, David M.
• Application Number:
  US07/100,104
• Time in Patent Office: 1,012 Days
• Field of Search: 252/315.3, 514/777, 424/7.1, 424/488, 536/4.1
• US Class Current: 514/777
• CPC Class Codes: A61K 47/36 Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
• CPC Class Codes: A61L 27/20 Polysaccharides
• 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 27/52 Hydrogels or hydrocolloids
• CPC Class Codes: A61L 31/041 Mixtures of macromolecular compounds
• CPC Class Codes: A61L 31/042 Polysaccharides
• CPC Class Codes: A61L 31/14 Materials characterised by their function or physical properties , e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
• CPC Class Codes: A61L 31/145 Hydrogels or hydrocolloids
• CPC Class Codes: C08B 37/0072 Hyaluronic acid, i.e. HA or hyaluronan; Derivatives thereof, e.g. crosslinked hyaluronic acid (hylan) or hyaluronates
• CPC Class Codes: C08L 1/28 Alkyl ethers
• CPC Class Codes: C08L 3/18 Ethers
• CPC Class Codes: C08L 5/08 Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof

Abstract

A method for making a water insouble bicompatible gel includes activating HA with an activating agent to form activated HA, and reacting the activated HA with a nucleophile, under conditions producing the water insoluble bicompatible gel. Also, a method for making a water insoluble biocompatible film includes providing a biocompatible gel made according to the above method, and drying the gel or compressing the gel under conditions permitting escape of water from the gel. Also, a water insoluble composition including HA is prepared without the use of any bifunctional or polyfunctional nucleophile.

Claims

1. A method for making a water insoluble biocompatible gel, said method comprising

providing an aqueous mixture comprising HA at a concentration in the range between 0.4% and 2.6% w/w,

activating said HA with an activating agent to form activated HA, and

reacting said activated HA with a nucleophile, under conditions producing said water insoluble biocompatible gel.

2. The method of claim 1 wherein said activating comprises

providing an aqueous mixture comprising said HA,

lowering the pH of said aqueous mixture to between 4.0 and 5.0 by addition of an acid, and then

contacting said aqueous mixture with said activating agent.

3. The method of claim 2 wherein said aqueous mixture comprises a concentration of said HA in the range between 0.4% and 2.6% w/w.

4. The method of claim 2 wherein said acid comprises hydrochloric acid.

5. The method of claim 1 wherein said HA and said activating agent are present during said activation at a molar ratio of at least 0.2 molar equivalent of activating agent to 1 molar equivalent of glucuronic acid residues of said HA.

6. The method of claim 1 wherein said activated HA and said nucleophile are present in said reacting step at a molar ratio of at least 0.2 molar equivalent of said nucleophile to 1 molar equivalent of glucuronic acid residues of said activated HA.

7. The method of claim 1 wherein said activating agent comprises a carbodiimide.

8. The method of claim 7 wherein said carbodiimide comprises 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide, or 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide methiodide.

9. The method of claim 1 wherein said nucleophile comprises an amino acid.

10. The method of claim 1 wherein said nucleophile comprises an amino acid salt.

11. The method of claim 1 wherein said nucleophile comprises an amino acid ester.

12. The method of claim 11 wherein said amino acid ester comprises a methyl ester.

13. The method of claim 11 wherein said amino acid ester comprises a butyl ester.

14. The method of claim 13 wherein said butyl ester comprises a t-butyl ester.

15. The method of claim 1 wherein said nucleophile comprises a methyl ester of an amino acid from the group comprising leucine, valine, isoleucine, arginine, proline, histidine, or phenylalanine.

16. The method of claim 1 wherein said nucleophile comprises L-leucine methyl ester hydrochloride, L-valine methyl ester hydrochloride, L-isoleucine methyl ester hydrochloride, L-arginine methyl ester hydrochloride, L-proline methyl ester hydrochloride, L-histidine methyl ester hydrochloride, L-phenylalanine hydrochloride, or L-leucine t-butyl ester hydrochloride.

17. The method of claim 1 wherein said nucleophile comprises an amino acid amide.

18. The method of claim 17 wherein said amino acid amide comprises leucinamide hydrochloride.

19. The method of claim 1 wherein said nucleophile comprises a monofunctional amine.

20. The method of claim 19 wherein said monofunctional amine comprises aniline.

21. A water insoluble biocompatible gel made according to the method of claim 1.

22. A method for making a water insoluble biocompatible film, said method comprising

providing the biocompatible gel of claim 21, and

drying said gel.

23. The film made by the method of claim 22.

24. A method for making a water insoluble biocompatible film, said method comprising

providing the biocompatible gel of claim 21, and

compressing said gel under conditions permitting escape of water from said gel.

25. The film made by the method of claim 24.

26. The method of claim 1 wherein said activating and said reacting occur concurrently.

27. The method of claim 1, said method further comprising admixing a detectable marker.

28. The method of claim 22 wherein said detectable marker comprises a dye that stains amino acids.

29. The method of claim 27 wherein said detectable marker comprises "Brilliant Blue R".

30. A water insoluble composition comprising HA, said composition being substantially free of crosslinking.

31. The composition of claim 30, said composition being substantially free of any bifunctional or polyfunctional nucleophile and said composition being substantially free of any bifunctional or polyfunctional electrophile.

32. The composition of claim 30, further comprising a monofunctional nucleophile.

33. The composition of claim 30, further comprising a monofunctional amine.

34. The composition of claim 30, further comprising a detectable marker.

35. The composition of claim 34, wherein said detectable marker comprises "Brilliant Blue R".

36. The composition of claim 30, further comprising a pharmaceutically active substance.

37. The composition of claim 36 wherein said pharmaceutically active substance is covalently bonded to said HA.

38. The composition of claim 36 wherein said pharmaceutically active substance is dispersed within said composition and is not covalently bonded to said composition.

40. The composition of claim 34, wherein said activating agent is a carbodiimide.

41. The composition of claim 40, wherein said carbodiimide is EDC.

42. The composition of claim 41, wherein said nucleophile is a methyl ester of an amino acid.

39. A water insoluble composition comprising the reaction product of HA, an activating agent, and a nucleophile.