IP Library Granted Patent US 11,780,970
Granted Patent B2
US 11,780,970 · App. 18/184,439 · Granted Oct 10, 2023

Carbohydrate crosslinker

Inventors: Hotan Mojarradi (Uppsala, SE); Johan Olsson (Bromma, SE); Craig Harris (Biot, FR); Jean-Guy Boiteau (Valbonne, FR); Thibaut Gerfaud (Mouans Sartoux, FR); Loïc Tomas (Biot, FR)
Assignee: GALDERMA HOLDING S.A.
C08J3/075A61K8/042A61K8/73A61K8/735A61K9/0019A61Q19/00C07C209/62C07C213/00C07C269/06C07F7/083C08B37/0063C08B37/0069C08B37/0072C08J3/24C08J7/14C08K5/09C08L5/00C08L5/08C07C2603/18C08J2305/00C08J2305/08
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Quick Facts
Patent No.
US 11,780,970
App. No.
18/184,439
Granted
Oct 10, 2023
Kind
B2
Abstract

The invention relates to a hydrogel product comprising glycosaminoglycan molecules as the swellable polymer, wherein the glycosaminoglycan molecules are covalently crosslinked via crosslinks comprising a spacer group selected from the group consisting of di-, tri-, tetra-, and oligosaccharides.

Claims (21)

1. A process of preparing a hydrogel product comprising crosslinked hyaluronic acid (HA) molecules, the process comprising:

hydrolyzing via alkaline hydrolysis ester bonds in HA molecules crosslinked by diaminotrehalose (DATH) via activated carboxyl groups, to obtain a hydrogel product having less than 50% non-crosslinked HA molecules by weight of the hydrogel product.

2. The process of claim 1 , further comprising crosslinking activated carboxyl groups of HA molecules using diaminotrehalose (DATH) to obtain the crosslinked HA molecules.

3. The process according to claim 2 , further comprising activating carboxyl groups of the HA molecules with a coupling agent to produce the activated carboxyl groups.

4. The process according to claim 3 , wherein the coupling agent is a triazine-based coupling reagent.

5. The process according to claim 3 , wherein the coupling agent is 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMTMM).

6. The process according to claim 3 , wherein the activating and the crosslinking occur simultaneously.

7. The process according to claim 1 , wherein amide bonds are formed between the HA molecules and the DATH.

8. The process according to claim 1 , wherein after the hydrolyzing, at least 90% of bonds between the HA molecules and the DATH are amide bonds.

9. The process according the claim 1 , wherein after the hydrolyzing, at least 95% of the bonds between the HA molecules and the DATH are amide bonds.

10. The process according to claim 1 , wherein after the hydrolyzing, less than 5% of bonds between the HA molecules and DATH are ester bonds.

11. The process according to claim 1 , wherein after the hydrolyzing, less than 1% of bonds between the HA molecules and DATH are ester bonds.

12. The process according to claim 1 , wherein the hydrolyzing comprises swelling the crosslinked HA molecules in an alkaline solution for at least 1 hour.

13. The process according to claim 1 , wherein less than 20% by weight of the hydrogel product comprises HA molecules that are not crosslinked.

14. The process according to claim 1 , wherein the crosslinked HA molecules are in the form of gel particles.

15. The process according to claim 12 , wherein the gel particles are 0.01 mm to 5 mm in size.

16. The process according to claim 2 , wherein the HA molecules, prior to the crosslinking, have a molecular weight of about 10 kDa to 10 MDa.

17. The process according to claim 16 , wherein the HA molecules, prior to the crosslinking, have a molecular weight of about 100 kDa to 1 MDa.

18. The process according to claim 1 , wherein the hydrogel product has an effective crosslinking ratio (CrR) of at least 0.43.

19. The process according to claim 1 , wherein the crosslinked HA molecules are free from synthetic non-carbohydrate structures and synthetic non-carbohydrate crosslinkers.

20. The process according to claim 1 , further comprising formulating the hydrogel product into an injectable composition.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 15, 2023
From: MOJARRADI, HOTAN; OLSSON, JOHAN; HARRIS, CRAIG; BOITEAU, JEAN-GUY
To: GALDERMA S.A.
Reel/Frame 062994/0378 →
CHANGE OF NAME Recorded Mar 15, 2023
From: NESTLE SKIN HEALTH S.A.
To: GALDERMA HOLDING S.A.
Reel/Frame 062994/0485 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 15, 2023
From: GALDERMA S.A.
To: NESTLE SKIN HEALTH S.A.
Reel/Frame 063101/0497 →
CHANGE OF ADDRESS Recorded Mar 15, 2023
From: GALDERMA HOLDING SA
To: GALDERMA HOLDING SA
Reel/Frame 063102/0576 →
Priority Claims (4)
EP 15202944 · Dec 29, 2015 · regional
EP 16172225 · May 31, 2016 · regional
EP 16172241 · May 31, 2016 · regional
EP 16172254 · May 31, 2016 · regional
Continuity (3)
Continuation 18071282
Continuation 16066810
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