IP Library Granted Patent US 10,988,600
Granted Patent B2
US 10,988,600 · App. 16/312,079 · Granted Apr 27, 2021

Cyclodextrin-grafted cross-linked hyaluronic acid complexed with active drug substances and uses thereof

Inventors: Katarina Edsman (Alunda, SE); Jean-Guy Boiteau (Valbonne, FR)
Assignee: GALDERMA HOLDING SA
C08L5/08A61K8/0283A61K8/735A61K9/0014A61K9/06A61K9/1694A61K47/36A61Q19/00C08B37/0012C08B37/0072C08J3/075C08J3/12C08K5/1515C08L5/16A61K31/216C08J2305/08C08J2305/16C08J2405/08C08J2405/16C08L2312/00
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Quick Facts
Patent No.
US 10,988,600
App. No.
16/312,079
Granted
Apr 27, 2021
Kind
B2
Abstract

A hyaluronic acid product is comprising a cross-linked hyaluronic acid and one or more cyclodextrin molecules, and further comprising a guest molecule capable of forming a guest-host complex with the aminocyclodextrin molecule acting as a host, wherein the guest molecule is a retinoid, preferably adapalene, or a RAM BA. The hyaluronic acid is cross-linked by ether bonds, and the one or more cyclodextrin molecules are grafted onto the cross-linked hyaluronic acid by amide bonds, preferably using a triazine-based coupling reagent.

Claims (27)

1. A hyaluronic acid product comprising:

(a) a cross-linked hyaluronic acid and one or more aminocyclodextrin host molecules, wherein the hyaluronic acid is cross-linked by ether bonds and wherein the one or more aminocyclodextrin host molecules are grafted onto the cross-linked hyaluronic acid by direct amide bonds between an amino group of the one or more aminocyclodextrin host molecules and a carboxyl group of the cross-linked hyaluronic acid; and

(b) one or more guest molecules comprising 4-(2-((5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)sulfonyl)ethyl)benzoic acid;

wherein the one or more guest molecules form a guest-host complex with the one or more aminocyclodextrin host molecules.

2. The hyaluronic acid product according to claim 1 , wherein the one or more aminocyclodextrin host molecules are constituted by 6-8 glucopyranoside units.

3. The hyaluronic acid product according to claim 2 , wherein the one or more aminocyclodextrin host molecules are selected from the group consisting of 2 aminocyclodextrin, 3-aminocyclodextrin, and 6-aminocyclodextrin.

4. The hyaluronic acid product according to claim 1 , wherein the one or more aminocyclodextrin host molecules and disaccharides of the cross-linked hyaluronic acid of the resulting hyaluronic acid product have a molar ratio of more than 2%.

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

6. A process of preparing a formulation of one or more guest molecules that form a guest-host complex with one or more aminocyclodextrin host molecules, the process comprising:

(a) providing (i) hyaluronic acid and (ii) one or more aminocyclodextrin host molecules with the one or more guest molecules comprising 4-(2-((5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)sulfonyl)ethyl)benzoic acid;

(b) cross-linking the hyaluronic acid by ether bonds using a bi- or polyfunctional cross-linking agent;

(c) grafting the one or more aminocyclodextrin host molecules onto the cross-linked hyaluronic acid by amide bonds; and

(d) bringing a solution of the one or more guest molecules into contact with the one or more aminocyclodextrin host molecules grafted onto the cross-linked hyaluronic acid under conditions allowing for the formation of the guest-host complex between the one or more aminocyclodextrin host molecules and the one or more guest molecules, and optionally

(e) recovering the guest-host complex bound to the cross-linked hyaluronic acid.

7. The process according to claim 6 , wherein an amino group of the aminocyclodextrin molecule forms said amide bond with a carboxyl group of the cross-linked hyaluronic acid.

8. The process according to claim 6 , wherein the grafting in (c) comprises:

(i) activating the carboxyl groups on the cross-linked hyaluronic acid with a triazine-based coupling reagent to form an activated cross-linked hyaluronic acid, and

(ii) coupling the one or more aminocyclodextrin molecules to the carboxyl groups of the activated cross-linked hyaluronic acid by amide bonds.

9. The process 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), ethylene glycol diglycidyl ether (EGDE), 1,2-ethanediol diglycidyl ether (EDDE), and diepoxyoctane.

10. The process according to claim 6 , further comprising providing particles of the hyaluronic acid product having an average size in the range of 0.01-5 mm.

11. A product obtainable by the process according to claim 6 .

12. A method of cosmetically treating skin, the method comprising administering to the skin the hyaluronic acid product according to claim 1 .

13. The hyaluronic acid product according to claim 5 , wherein the hyaluronic acid product is in the form of gel particles having an average size in the range of 0.1-0.8 mm.

14. The hyaluronic acid product according to claim 1 , wherein the one or more aminocyclodextrin host molecules comprise methyl groups or hydroxypropyl groups.

15. The hyaluronic acid product according to claim 1 , wherein the one or more guest molecules are capable of being released from the guest-host complexes due to a change in pH that cleaves hydrogen or ionic bonds between the host and guest molecules.

16. The hyaluronic acid product according to claim 1 , wherein the one or more guest molecules are capable of being released from the guest-host complexes due to enzymatic cleavage of α-1,4 linkages between glucose monomers.

17. The hyaluronic acid product according to claim 4 , wherein the one or more aminocyclodextrin host molecules and disaccharides of the cross-linked hyaluronic acid of the resulting hyaluronic acid product have a molar ratio of more than 5%.

Assignments (5)
CHANGE OF ADDRESS Recorded Jun 28, 2022
From: GALDERMA HOLDING SA
To: GALDERMA HOLDING SA
Reel/Frame 060541/0374 →
CORRECTIVE ASSIGNMENT TO CORRECT THE THE ASSIGNEES ADDRESS PREVIOUSLY RECORDED AT REEL: 057652 FRAME: 0859. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Dec 13, 2021
From: GALDERMA S.A.
To: NESTLÉ SKIN HEALTH S.A.
Reel/Frame 058495/0582 →
CHANGE OF NAME Recorded Sep 29, 2021
From: NESTLÉ SKIN HEALTH S.A.
To: GALDERMA HOLDING SA
Reel/Frame 057631/0589 →
AMENDMENT TO ASSET TRANSFER AGREEMENT Recorded Sep 29, 2021
From: GALDERMA S.A.
To: NESTLÉ SKIN HEALTH S.A.
Reel/Frame 057652/0859 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2020
From: EDSMAN, KATARINA; BOITEAU, JEAN-GUY
To: GALDERMA S.A.
Reel/Frame 052507/0161 →