IP Library › Granted Patent US 8,574,629
Granted Patent B2
US 8,574,629 · App. 12/512,581 · Granted Nov 5, 2013

Injectable hydrogel with an enhanced remanence and with an enhanced ability to create volume

Inventor: Samuel Gavard Molliard (Bogeve, FR)
Assignee: Anteis S.A.
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Quick Facts
Patent No.
US 8,574,629
App. No.
12/512,581
Granted
Nov 5, 2013
Kind
B2
Abstract

An injectable hydrogel includes a hydrogel matrix based on (a) single-phase-type cross-linked biopolymer(s), characterized in that previously cross-linked biopolymer hydrogel particles are co-cross-linked with the matrix. A method of and a process for production of the above-mentioned hydrogel are also disclosed.

Claims (24)

1. An injectable hydrogel that comprises:

a hydrogel matrix comprising single phase cross-linked biopolymer(s), and

previously cross-linked biopolymer hydrogel particles co-cross-linked with said matrix,

wherein the biopolymer(s) is (are) selected from the group consisting of sodium hyaluronate, chondroitin sulfate, keratan, keratan sulfate, heparin, heparan sulfate, cellulose and its derivatives, alginates, xanthan, carrageenan, proteins, nucleic acids and mixtures thereof,

the total biopolymer concentration is between 0.01 and 100 mg/ml,

the mass percent of particles in the single-phase matrix is between 1 and 99%, and

the particles have an inside diameter of between 50 and 1000 micrometers.

2. The injectable hydrogel according to claim 1 , wherein the biopolymer is sodium hyaluronate.

3. The injectable hydrogel according to claim 1 , wherein the hydrogel particles have the following shapes: spherical, elliptical, or irregular shapes, or they have several of these shapes.

4. The injectable hydrogel according to claim 1 , wherein the biopolymer particles are distributed and co-cross-linked homogeneously inside the hydrogel matrix.

5. The injectable hydrogel according to claim 1 , further comprising at least one additive.

6. The injectable hydrogel according to claim 1 , further comprising at least one pharmacologically active agent.

7. The injectable hydrogel according to claim 1 , wherein the total biopolymer concentration is between 10 and 40 mg/ml.

8. The injectable hydrogel according to claim 1 , further comprising at least one additive.

9. The injectable hydrogel according to claim 6 , wherein the at least one pharmacologically active agent is a steroidal anti-inflammatory agent.

10. The injectable hydrogel according to claim 1 , further comprising at least one anti-oxidizing agent.

11. The injectable hydrogel according to claim 1 , further comprising at least one compound that makes the gel better able to resist in vivo degradation.

12. The injectable hydrogel according to claim 11 , wherein the at least one compound is a polyol.

13. The injectable hydrogel according to claim 1 , having an osmolarity of 301-314 mOsm/kg.

14. The injectable hydrogel according to claim 1 , having an ejection force of 42-61 N.

15. The injectable hydrogel according to claim 1 , having an elasticity of 352-441 G′ at 1 Hz.

16. The injectable hydrogel according to claim 8 , wherein the at least one additive is a pH modifier or an osmolarity adjuster.

17. The injectable hydrogel according to claim 9 , wherein the steroidal anti-inflammatory is triamcinolone acetonide.

18. The injectable hydrogel according to claim 1 , wherein the cross-linking agent is butanediol diglycidyl ether.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2009
From: GAVARD MOLLIARD, SAMUEL
To: ANTEIS S.A.
Reel/Frame 023251/0519 →
Priority Claims (1)
FR 08 04416 · Aug 1, 2008 · national
Continuity (1)
Related Publication 20100028435A1 · Feb 4, 2010