IP Library Granted Patent US 9,283,301
Granted Patent B1
US 9,283,301 · App. 13/713,685 · Granted Mar 15, 2016

Shape-memory sponge hydrogel biomaterial

Inventors: Dan Simionescu (Pendleton, SC); Jeremy J. Mercuri (Easley, SC)
Assignee: Clemson University
A61L27/24A61F2/02A61F2/441
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Quick Facts
Patent No.
US 9,283,301
App. No.
13/713,685
Granted
Mar 15, 2016
Kind
B1
Abstract

A hydrogel biomaterial that can be utilized as a nucleus pulposus replacement material is described. The hydrogel biomaterial can is an elastin-glycosaminoglycan-collagen composite hydrogel biomaterial that can mimic the biochemical and functional characteristics of the human nucleus pulposus. Methods for forming the hydrogel biomaterial are also described as are methods for use of the hydrogel biomaterial, one of which is as an in vivo nucleus pulposus replacement material, another of which is a scaffolding material for use in nucleus pulposus tissue engineering applications.

Claims (15)

1. A method for forming a hydrogel biomaterial comprising:

combining collagen, soluble elastin, and at least one glycosaminoglycan to form a mixture;

heating the mixture to form a gel;

crosslinking the gel with a first crosslinking agent, the first crosslinking agent forming crosslinks between the collagen and the at least one glycosaminoglycan;

crosslinking the gel with a second crosslinking agent, the second crosslinking agent stabilizing the soluble elastin; and

degrading only a portion of the gel following crosslinking with the first and second crosslinking agents with one or more enzymes that target the at least one glycosaminoglycan to form the hydrogel biomaterial, the formed hydrogel, biomaterial exhibiting an equilibrium modulus of from about 3 kilopascals to about 10 kilopascals.

2. The method of claim 1 , wherein the mixture is formed at a temperature of less than about 20° C.

3. The method of claim 1 , wherein the mixture is heated to a temperature of from about 30° C. to about 40° C. to form the gel.

4. The method of claim 1 , wherein the first crosslinking agent is ethyl-3-(-3-dimethylaminopropyl) carbodiimide hydrochloride.

5. The method of claim 1 , wherein the first crosslinking agent is provided in conjunction with N-hydroxysuccinimide or a water-soluble analog thereof.

6. The method of claim 5 , wherein the N-hydroxysuccinimide is provided in a concentration of about 6 mM or greater.

7. The method of claim 1 , wherein the first crosslinking agent is provided in a concentration of about 30 mM or greater.

8. The method of claim 1 , wherein the second crosslinking agent is a phenolic compound comprising a hydrophobic core and a plurality of phenol groups extending from the hydrophobic core.

9. The method of claim 1 , wherein the second crosslinking agent is pentagalloylglucose.

10. The method of claim 1 , wherein the one or more enzymes are provided at a total enzymatic concentration of less than about 10 U/ml.

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 14, 2015
From: CLEMSON UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 036607/0143 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2014
From: SIMIONESCU, DAN; MERCURI, JEREMY J.
To: CLEMSON UNIVERSITY
Reel/Frame 032857/0676 →
Continuity (1)
Provisional Application 61570374 · Dec 14, 2011