Method for preparing acylated crosslinked glycosaminoglycans

US11939433B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11939433-B2
Application numberUS-202318208527-A
CountryUS
Kind codeB2
Filing dateJun 12, 2023
Priority dateDec 29, 2015
Publication dateMar 26, 2024
Grant dateMar 26, 2024

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

Official abstract text for this publication.

A method of preparing a hydrogel product including crosslinked glycosaminoglycan molecules, said method including: i) providing a glycosaminoglycan crosslinked by amide bonds, wherein the crosslinked glycosaminoglycans include residual amine groups; and ii) acylating residual amine groups of the crosslinked glycosaminoglycans provided in i) to form acylated crosslinked glycosaminoglycans.

First claim

Opening claim text (preview).

The invention claimed is: 1. A hydrogel product comprising acylated crosslinked glycosaminoglycans (GAGs), produced by a method comprising: crosslinking (i) an at least partially deacetylated GAG comprising free amine groups and (ii) a second GAG comprising activated carboxyl groups, by forming amide bonds between 2′-amino groups on the at least partially deacetylated GAG and the activated carboxyl groups of the second GAG, wherein the hydrogel product has residual free amine groups and a degree of acetylation of at least 95%. 2. The hydrogel product according to claim 1 , wherein the at least partially deacetylated GAG is selected from the group consisting of deacetylated hyaluronic acid, deacetylated chondroitin, and deacetylated chondroitin sulfate, and mixtures thereof. 3. The hydrogel product according to claim 2 , wherein the at least partially deacetylated GAG is deacetylated hyaluronic acid. 4. The hydrogel product according to claim 1 , wherein the at least partially deacetylated GAG has a degree of acetylation of 95% or less, and a weight average molecular weight of 0.1 MDa or more. 5. The hydrogel product according to claim 1 , wherein the at least partially deacetylated GAG is prepared by: (a) allowing a GAG comprising N-acetyl groups to react with hydroxylamine (NH 2 OH), or a salt thereof, at a temperature of 100° C. or less for 2-200 hours to form the at least partially deacetylated GAG, and (b) recovering the at least partially deacetylated GAG. 6. The hydrogel product according to claim 1 , wherein the second GAG is selected from the group consisting of hyaluronic acid, chondroitin, and chondroitin sulfate, and mixtures thereof. 7. The hydrogel product according to claim 6 , wherein the second GAG is hyaluronic acid. 8. The hydrogel product according to claim 1 , wherein the activated carboxyl groups on the second GAG are formed using a coupling agent. 9. The hydrogel product according to claim 8 , wherein the coupling agent is a peptide coupling reagent. 10. The hydrogel product according to claim 8 , wherein the coupling reagent is DMTMM. 11. The hydrogel product according to claim 1 , wherein the method of producing the acylated crosslinked GAGs further comprises acetylating residual free amine groups of the crosslinked GAGs. 12. The hydrogel product according to claim 1 , wherein the method of producing the acylated crosslinked GAGs further comprises hydrolyzing ester crosslinks formed as byproducts during the crosslinking by subjecting the crosslinked acetylated GAGs to alkaline solution. 13. The hydrogel product according to claim 12 , wherein the alkaline solution comprises sodium hydroxide or potassium hydroxide. 14. The hydrogel product according to claim 13 , wherein the hydrolyzing is performed in sodium hydroxide solution at a pH of 12 to 14, for 0.5 to 4 hours. 15. The hydrogel product according to claim 1 , wherein the hydrogel product is in a solid, dry form. 16. The hydrogel product according to claim 1 , wherein the at least partially deacetylated GAG has a weight average molecular weight of 0.5 MDa or more. 17. The hydrogel product according to claim 1 , wherein the crosslinked GAGs are substantially free of ester crosslinks. 18. The hydrogel product according to claim 1 , wherein the crosslinked GAGs comprise two different GAGs selected from hyaluronic acid, chondroitin, chondroitin sulphate, heparin sulphate, heparosan, heparin, dermatan sulphate, and keratin sulphate. 19. The hydrogel product according to claim 1 , wherein the second GAG is non-deacetylated. 20. A composition comprising: the hydrogel product according to claim 1 ; and water.

Assignees

Inventors

Classifications

  • General cosmetic use · CPC title

  • Preparations for care of the skin · CPC title

  • Gels · CPC title

  • Mucopolysaccharides, e.g. hyaluronic acid; Derivatives thereof · CPC title

  • Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin · CPC title

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What does patent US11939433B2 cover?
A method of preparing a hydrogel product including crosslinked glycosaminoglycan molecules, said method including: i) providing a glycosaminoglycan crosslinked by amide bonds, wherein the crosslinked glycosaminoglycans include residual amine groups; and ii) acylating residual amine groups of the crosslinked glycosaminoglycans provided in i) to form acylated crosslinked glycosaminoglycans.
Who is the assignee on this patent?
Galderma Holding SA, Galderma Holding S A
What technology area does this patent fall under?
Primary CPC classification C08J3/075. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Mar 26 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).