IP Library › Granted Patent US 10,618,983
Granted Patent B2
US 10,618,983 · App. 15/580,671 · Granted Apr 14, 2020

Hyaluronic acid-based hydrogels having medical applications

Inventors: Samir Mitragotri (Santa Barbara, CA); Stefano Menegatti (Raleigh, NC)
Assignee: The Regents of the University of California
C08B37/0072A61K31/728A61K45/06A61L27/20A61L27/38A61L27/52A61L27/54A61M5/19A61M5/31596C07K16/283C08J3/075C08L5/08A61K9/0014A61K9/06A61K47/36A61L2300/402A61L2300/406A61L2300/414A61L2300/436A61L2400/06A61M2210/04
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Quick Facts
Patent No.
US 10,618,983
App. No.
15/580,671
Granted
Apr 14, 2020
Kind
B2
Abstract

Provided herein are novel hyaluronic acid-based materials for in-situ gelation in wounds and other contexts, which materials are biocompatible and which have favorable gelation kinetics. The resulting hydrogels have desirable rheological properties. The invention encompasses novel reagents for forming crosslinked hyaluronic acid hydrogels, with favorable kinetics for medical applications and having desirable and tunable physical properties. Also presented herein are methods of using the novel materials disclosed herein in wound care and other medical contexts.

Claims (29)

1. A system for forming a gel comprising,

first and second functionalized hyaluronic acid (“HA”) polymers, wherein:

the first functionalized HA polymer comprises a first HA polymer moiety functionalized with a first reactive moiety that reacts with a second reactive moiety;

the second functionalized HA polymer comprises a second HA polymer moiety functionalized with the second reactive moiety, which second reactive moiety comprises D-Cys or a D-Cys mimetic;

wherein the first reactive moiety comprises CBT, a CBT mimetic, or another molecule that reacts with either the —SH or the —NH 2 group of D-Cys; and

when the first and second functionalized HA polymers are brought together the first and second reactive moieties react to cross-link the functionalized polymers and form the gel.

2. The system of claim 1 , wherein

the first reactive moiety increases the hydrophobicity of the functionalized first polymer relative to unfunctionalized first polymer moiety.

3. The system of claim 2 , wherein

the second reactive moiety is or comprises D-Cys.

4. The system of claim 3 , wherein

the first reactive group is or comprises cyanobenzothiazole.

5. A method of forming a gel in situ in an intradermal site, the method comprising

topically applying a first functionalized hyaluronic acid (“HA”) polymer and a second functionalized hyaluronic acid (“HA”) polymer;

wherein the first functionalized HA polymer comprises a first HA polymer moiety functionalized with a first reactive moiety that reacts with a second reactive moiety;

wherein the second functionalized HA polymer comprises a second HA polymer moiety functionalized with the second reactive moiety, which second reactive moiety comprises D-Cys or a D-Cys mimetic; and

wherein at least the first functionalized HA polymer penetrates the skin, whereat its first reactive moiety reacts with the second reactive moiety, thereby crosslinking the first and second polymer moieties to one another.

6. The method of claim 5 , wherein

the first reactive moiety increases the hydrophobicity of the first polymer moiety.

7. The method of claim 6 , wherein

the first reactive moiety is or comprises CBT.

8. The method of claim 7 , wherein

the second reactive moiety is or comprises D-Cys.

9. The method of claim 5 , wherein

the first functionalized polymer and second functionalized polymers are applied to a wound.

10. The method of claim 5 , wherein

the first polymer and the second polymer react after transport across the stratum corneum.

11. The method of claim 5 , wherein

the first reactive moiety and the second reactive moiety form a cross-link which is fluorescent.

Continuity (2)
Provisional Application 62174171 · Jun 11, 2015
Related Publication 20180186900A1 · Jul 5, 2018
Cited By (1)
US 12,714,357