IP Library Granted Patent US 9,034,355
Granted Patent B2
US 9,034,355 · App. 13/403,557 · Granted May 19, 2015

Materials for modulating biological responses and methods of making

Inventors: Melissa M. Reynolds (Fort Collins, CO); Vinod B. Damodaran (Fort Collins, CO)
Assignee: Colorado State University Research Foundation
A61K47/4823A61K47/482A61K33/00
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Quick Facts
Patent No.
US 9,034,355
App. No.
13/403,557
Granted
May 19, 2015
Kind
B2
Abstract

A polymeric composition capable of releasing nitric oxide and modulating biological responses comprises a biocompatible polymer and S-nitrosated thiol bonded to the biocompatible polymer. The polymeric composition can have a thiol conversion of at least 40%. The polymeric composition can also have a nitric oxide recovery of at least 40% when under thermal decomposition conditions.

Claims (18)

1. A method of forming a nitric oxide releasing biocompatible polymer for modulating biological response, the method comprising:

a. activating carboxyl groups of a biocompatible polymer in a non-aqueous solution by reaction with N-hydroxysuccinimide; and

b. converting thiol residues on the biocompatible polymer to S-nitrosated residues under non-aqueous conditions, wherein at least about 40% of thiol residues are converted to S-nitrosated residues.

2. The method of claim 1 , wherein the nitric oxide releasing biocompatible polymer comprises at least about 0.1 mmol of nitric oxide per 1 gram of the nitric oxide releasing biocompatible polymer.

3. The method of claim 1 , wherein the nitric oxide releasing biocompatible polymer comprises at least about 0.4 mmol of nitric oxide per 1 gram of the nitric oxide releasing biocompatible polymer.

4. The method of claim 1 , wherein the method further comprises forming the biocompatible polymer into a nanofiber after converting the thiol residues.

5. The method of claim 1 , wherein the S-nitrosated residues are residues from at least one member selected from the group consisting of: cysteamine, cysteine, and homocysteine.

6. The method of claim 1 , wherein the biocompatible polymer comprises a member selected from the group consisting of: polylactide, polyglycolide, poly(lactide-co-glycolide), poly(ε-caprolactone), chitosan and dextran.

7. The method of claim 1 , wherein the biocompatible polymer comprises poly(lactide-co-glycolide).

8. The method of claim 7 , wherein the S-nitrosated residues include residues from cysteamine.

9. The method of claim 7 , wherein the S-nitrosated residues include residues from cysteine.

10. The method of claim 7 , wherein the S-nitrosated residues include residues from homocysteine.

11. The method of claim 1 , wherein the biocompatible polymer comprises poly(lactic-co-glycolic-co-hydroxymethyl propionic acid).

12. The method of claim 1 , wherein the biocompatible polymer comprises dextran.

13. The method of claim 12 , wherein the S-nitrosated residues include residues from cysteine.

14. The method of claim 12 , wherein the S-nitrosated residues include residues from cysteamine.

15. The method of claim 1 , wherein the biocompatible polymer comprises chitosan.

16. The method of claim 1 , wherein the biocompatible polymer comprises dextran and poly(lactic-co-glycolic-co-hydroxymethyl propionic acid).

Assignments (3)
CONFIRMATORY LICENSE Recorded Dec 14, 2015
From: COLORADO STATE UNIVERSITY RESEARCH FOUNDATION
To: US ARMY, SECRETARY OF THE ARMY
Reel/Frame 037279/0320 →
CONFIRMATORY LICENSE Recorded Aug 1, 2012
From: COLORADO STATE UNIVERSITY RESEARCH FOUNDATION
To: US ARMY, SECRETARY OF THE ARMY
Reel/Frame 028699/0661 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 28, 2012
From: REYNOLDS, MELISSA M.; DAMODARAN, VINOD B.
To: COLORADO STATE UNIVERSITY RESEARCH FOUNDATION
Reel/Frame 027772/0788 →
Continuity (2)
Provisional Application 61446121 · Feb 24, 2011
Related Publication 20150004257A1 · Jan 1, 2015