IP Library Granted Patent US 10,195,304
Granted Patent B2
US 10,195,304 · App. 15/035,831 · Granted Feb 5, 2019

Functionalized microgels with fibrin binding elements

Inventors: Thomas H. Barker (Atlanta, GA); Ashley Carson Brown (Atlanta, GA); Louis Andrew Lyon (Irvine, CA); Sarah E. Stabenfeldt (Tempe, AZ); Nicole Welsch (Berlin, DE)
Assignee: Georgia Tech Research Corporation
A61L24/0015A61L24/046A61L24/06A61L26/0047A61L27/227A61L2300/418A61L2400/04
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Quick Facts
Patent No.
US 10,195,304
App. No.
15/035,831
Granted
Feb 5, 2019
Kind
B2
Abstract

Ultra-low crosslinked microgels made of an ultra-low crosslinked polymer are provided. The microgels, also referred to as Platelet-like Particles (PLPs), preferably have <0.5% crosslinking densities. One or more of the polymers are conjugated with a fibrin-binding element or moiety, preferably H6, in an amount effective to confer to the microgel selective binding to fibrin under physiological conditions. The PLPs can recapitulate multiple key functions of platelets including binding, stabilizing and enhancing fibrin clot formation, responsiveness to injury cues, and induction of clot contraction. In a preferred embodiment, the microgel or PLP has little or no binding to soluble fibrinogen under physiological conditions compared to its binding to fibrin. The microgels or PLPs are prepared using crosslinker-free synthesis conditions, and can promote or induce clotting and clot contraction.

Claims (16)

1. An ultra-low crosslinked microgel comprising an ultra-low crosslinked polymer having <0.5% crosslinking densities, wherein the microgel comprises a binding moiety specific for fibrin conjugated to the exterior of the microgel, and wherein the binding moiety comprises the amino acid sequence of SEQ ID NO:1 (H6) and has little or no binding to soluble fibrinogen under physiological conditions compared to its binding to fibrin.

2. The microgel of claim 1 , wherein the polymer is poly(N-isopropylacrylamide-co-acrylic acid).

3. The microgel of claim 2 , wherein the composition of the polymer is 95:5 molar ratio of N-isopropylacrylamide to acrylic acid.

4. The microgel of claim 1 , wherein the binding moiety specific for fibrin is present on the surface of the microgel at a density of 9.98×10 −11 mg/particle.

5. The microgel of claim 1 , wherein the microgel is formed under crosslinker-free synthesis conditions.

6. The microgel of claim 1 , wherein the microgel has a diameter of about 1 μm in solution.

7. A pharmaceutical composition comprising:

a microgel according to claim 1 ; and

a pharmaceutically acceptable excipient.

8. A kit comprising:

any one of the microgels according to claim 1 formulated into a unit dose; and

a bandage.

9. A wound dressing comprising:

a dressing comprising any one of the microgels according to claims 1 - 2 , 3 , and 4 - 6 .

10. A medical device coated with the microgel of claim 1 .

11. The medical device of claim 10 , wherein the medical device is selected from the group consisting of a clamp, suture, and staple.

Assignments (2)
CONFIRMATORY LICENSE Recorded Feb 28, 2018
From: GEORGIA INSTITUTE OF TECHNOLOGY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 045469/0259 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 11, 2016
From: BARKER, THOMAS H.; BROWN, ASHLEY CARSON; LYON, LOUIS ANDREW; STABENFELDT, SARAH E.; WELSCH, NICOLE
To: GEORGIA TECH RESEARCH CORPORATION
Reel/Frame 038545/0955 →
Continuity (2)
Provisional Application 61902489 · Nov 11, 2013
Related Publication 20160271292A1 · Sep 22, 2016