IP Library Granted Patent US 10,131,718
Granted Patent B2
US 10,131,718 · App. 15/314,168 · Granted Nov 20, 2018

Cross-linked hyaluronic acid grafted with dextran

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Quick Facts
Patent No.
US 10,131,718
App. No.
15/314,168
Granted
Nov 20, 2018
Kind
B2
Abstract

A hyaluronic acid product is comprising a cross-linked hyaluronic acid and one or more dextran molecules. The hyaluronic acid is cross-linked by ether bonds, and the one or more dextran molecules are covalently grafted to the cross-linked hyaluronic acid.

Claims (38)

1. A hyaluronic acid product comprising a cross-linked hyaluronic acid and one or more dextran molecules, wherein the hyaluronic acid is cross-linked by ether bonds and the one or more dextran molecules are covalently grafted to the cross-linked hyaluronic acid, wherein the dextran molecules are covalently linked to the hyaluronic acid by single end-point attachment via a bi- or polyfunctional linker between the reducing end of dextran and a carboxyl group of hyaluronic acid.

2. A hyaluronic acid product according to claim 1 , wherein the cross-linked hyaluronic acid is in the form of a gel.

3. A hyaluronic acid product according to claim 1 , wherein the cross-linked hyaluronic acid is in the form of gel particles having an average size in the range of 0.01-5 mm.

4. A hyaluronic acid product according to claim 1 , wherein the hyaluronic acid chains are cross-linked to each other via a linker which is derived from a bi- or polyfunctional cross-linking agent.

5. A hyaluronic acid product according to claim 4 , wherein said bi- or polyfunctional cross-linking agent is a bis- or polyepoxide.

6. A hyaluronic acid product according to claim 5 , wherein said bi- or polyfunctional cross-linking agent is a diglycidyl ether.

7. A hyaluronic acid product according to claim 6 , wherein said bi- or polyfunctional cross-linking agent is selected from the group consisting of 1,4-butanediol diglycidyl ether (BDDE), 1,2-bis(2,3-epoxypropoxy)ethylene (EGDGE) and ethylene glycol diglycidyl ether (EGDE), 1,2-ethanediol diglycidyl ether (EDDE) and diepoxyoctane.

8. A hyaluronic acid product according to claim 7 , wherein said bi- or polyfunctional cross-linking agent is 1,4-butanediol diglycidyl ether (BDDE).

9. A hyaluronic acid product according to claim 1 , wherein the one or more dextran molecules and the disaccharides of the cross-linked hyaluronic acid have a molar ratio of 0.1-99%.

10. A hyaluronic acid product according to claim 1 , wherein the one or more dextran molecules and the disaccharides of the cross-linked hyaluronic acid have a molar ratio of 1-60%.

11. A hyaluronic acid product according to claim 1 , wherein the dextran molecules have an average molecular weight of less than 10 kDa.

12. A hyaluronic acid product according to claim 1 , wherein the dextran molecules have an average molecular weight of less than 5 kDa.

13. A hyaluronic acid product according to claim 1 , wherein the dextran molecule contains a linker having an amino, hydrazide, carbazate, semicarbazide, thiosemicarbazide, thiocarbazate or aminooxy functional group, and wherein the functional group of the linker forms a covalent bond with a carboxyl group of the cross-linked hyaluronic acid.

14. A hyaluronic acid product according to claim 13 , wherein the bi- or polyfunctional linker comprises a diamine or a dihydrazide.

15. A hyaluronic acid product according to claim 1 , wherein the one or more dextran molecules are covalently grafted to the cross-linked hyaluronic acid by amide bonds.

16. A process of preparing a hyaluronic acid product comprising a cross-linked hyaluronic acid and one or more dextran molecules, the process comprising the steps of:

(a) providing a cross-linked hyaluronic acid and one or more functionalized dextran molecules;

(b) covalently grafting one or more functionalized dextran molecules to the cross-linked hyaluronic acid;

wherein the functionalized dextran molecules provided in step (a) are functionalized at the reducing end with a bi- or polyfunctional linker having at least one functional group available for linking the dextran molecules to a carboxyl group of the cross-linked hyaluronic acid.

17. A process according to claim 16 , wherein the cross-linked hyaluronic acid in step (a) is in the form of a gel.

18. A process according to claim 16 , wherein the cross-linked hyaluronic acid in step (a) is in the form of gel particles having an average size in the range of 0.01-5 mm.

19. A process according to claim 16 , wherein the one or more dextran molecules and the disaccharides of the cross-linked hyaluronic acid of the resulting hyaluronic acid product have a molar ratio of 0.1-99%.

20. A process according to claim 16 , wherein the one or more dextran molecules and the disaccharides of the cross-linked hyaluronic acid of the resulting hyaluronic acid product have a molar ratio of 1-60%.

21. A process according to claim 16 , wherein the dextran molecules provided in step (a) have an average molecular weight of less than 10 kDa.

22. A process according to claim 16 , wherein the dextran molecules provided in step (a) have an average molecular weight of less than 5 kDa.

23. A process according to claim 16 , wherein the one or more functionalized dextran molecules of step (a) contain a linker having an amino, hydrazide, carbazate, semicarbazide, thiosemicarbazide, thiocarbazate or aminooxy functional group, and wherein the functional group of the linker forms a covalent bond with a carboxyl group of the cross-linked hyaluronic acid.

24. A process according to claim 23 , wherein the bi- or polyfunctional linker comprises a diamine or a dihydrazide.

25. A process according to claim 16 , wherein the covalent grafting of step (b) involves:

(i) activating the carboxyl groups on the cross-linked hyaluronic acid with a coupling agent to form an activated cross-linked hyaluronic acid; and

(ii) coupling the linker of the one or more functionalized dextran molecules to the carboxyl groups of the activated cross-linked hyaluronic acid.

26. A process according to claim 25 , wherein the activation of the cross-linked hyaluronic acid and the coupling of the dextran molecule to the activated cross-linked hyaluronic acid occur simultaneously in step (b).

27. A process according to claim 25 , wherein the activation of the cross-linked hyaluronic acid occurs prior to and separately from the coupling of the one or more dextran molecules to the activated cross-linked hyaluronic acid in step (b).

28. A process according to claim 25 , wherein the coupling agent is selected from the group consisting of triazine-based coupling agents, carbodiimide coupling agents, imidazolium-derived coupling agents, Oxyma and COMU.

29. A process according to claim 28 , wherein the coupling agent is a triazine-based coupling agent.

30. A process according to claim 29 , wherein the triazine-based coupling agent is selected from the group consisting of 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMTMM) and 2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT).

31. A process according to claim 30 , wherein the triazine-based coupling agent is DMTMM.

32. A hyaluronic acid product obtainable by the process according to claim 16 .

33. A hyaluronic acid product according to claim 1 for use as a dermal filler.

Assignments (3)
ASSET TRANSFER AGREEMENT Recorded Oct 3, 2021
From: GALDERMA S.A.
To: NESTLÉ SKIN HEALTH S.A.
Reel/Frame 057698/0295 →
CHANGE OF NAME Recorded Oct 3, 2021
From: NESTLÉ SKIN HEALTH S.A.
To: GALDERMA HOLDING SA
Reel/Frame 057698/0356 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 29, 2016
From: KARLSSON, ANDERS; MOJARRADI, HOTAN
To: GALDERMA S.A.
Reel/Frame 040803/0170 →
Cited By (1)
US 12,714,768