IP Library Granted Patent US 10,293,077
Granted Patent B2
US 10,293,077 · App. 14/883,224 · Granted May 21, 2019

Polyphosphate-functionalized inorganic nanoparticles as hemostatic compositions and methods of use

Inventors: Damien Kudela (Santa Barbara, CA); Galen D. Stucky (Santa Barbara, CA); Anna May-Masnou (Barcelona, ES); Gary Bernard Braun (San Diego, CA); James H. Morrissey (Champaign, IL); Stephanie A. Smith (Urbana, IL)
Assignees: The Regents of the University of California; The Board of Trustees of the University of Illinois
A61L24/046A61K47/595A61K47/6923A61K47/6935A61L24/02A61L2300/404A61L2300/418A61L2400/04A61L2400/12Y10T428/2982
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Quick Facts
Patent No.
US 10,293,077
App. No.
14/883,224
Granted
May 21, 2019
Kind
B2
Abstract

A hemostatic composition is provided. The hemostatic composition includes a hemostatically effective amount of a hemostatic agent that includes a nanoparticle and a polyphosphate polymer attached to the nanoparticle. Also provided are medical devices and methods of use to promote blood clotting.

Claims (34)

1. A hemostatic composition comprising a hemostatically effective amount of a hemostatic agent comprising:

a material selected from the group consisting of iron oxide, diatomaceous earth, an aluminosilicate, an oxide of a transition metal, and titanium dioxide, wherein the material is a nanoparticle; and

a polyphosphate polymer covalently attached to the nanoparticle.

2. The hemostatic composition of claim 1 , wherein the polyphosphate polymer is attached to the nanoparticle through a linkage selected from the group consisting of an ester linkage and a carboxylic acid linkage.

3. The hemostatic composition of claim 1 , wherein the nanoparticle comprises a surface functionalized with (3-aminopropyl)triethoxysilane (APTES).

4. The hemostatic composition of claim 3 , wherein the polyphosphate polymer is attached to the nanoparticle through a phosphoramidate linkage.

5. The hemostatic composition of claim 1 , wherein the hemostatic agent further comprises a protecting agent attached to the hemostatic agent by an enzymatically-cleavable linking group.

6. The hemostatic composition of claim 5 , wherein the enzymatically-cleavable linking group is cleavable by an enzyme selected from the group consisting of thrombin (Factor IIa), Factor VIIa, Factor IXa, Factor Xa, Factor XIa, Factor XIIa, tissue plasminogen activator (tPA), urokinase plasminogen activator (uPA), activated protein C, and plasmin.

7. The hemostatic composition of claim 5 , wherein the protecting agent comprises a polyethylene glycol polymer.

8. The hemostatic composition of claim 7 , wherein the polyethylene glycol polymer has a molecular mass of 1000 Da to 10,000 Da.

9. The hemostatic composition of claim 7 , wherein the polyethylene glycol polymer has a molecular mass of 1000 Da to 20,000 Da.

10. The hemostatic composition of claim 1 , wherein the hemostatic agent further comprises a specific binding agent.

11. The hemostatic composition of claim 10 , wherein the specific binding agent specifically binds to a protein or a peptide.

12. The hemostatic composition of claim 11 , wherein the specific binding agent comprises a protein binding aptamer or peptide.

13. The hemostatic composition of claim 11 , wherein the specific binding agent comprises a fibrin binding ligand.

14. The hemostatic composition of claim 13 , wherein the specific binding agent comprises CREKA (SEQ ID NO: 1).

15. The hemostatic composition of claim 1 , further comprising a biologically active agent bound to the hemostatic agent.

16. The hemostatic composition of claim 15 , wherein the biologically active agent is selected from the group consisting of an enzyme, a phospholipid, a clotting cascade cofactor, an antibiotic, and an anti-inflammatory agent.

17. The hemostatic composition of claim 1 , wherein the polyphosphate polymer comprises 20 to 1500 phosphate monomers.

18. The hemostatic composition of claim 1 , wherein the hemostatic agent has a polyphosphate polymer to nanoparticle mass ratio of 1:1 to 1:5.

19. The hemostatic composition of claim 1 , wherein the nanoparticle has an average diameter of 750 nm or less.

20. The hemostatic composition of claim 1 , wherein the nanoparticle has an average diameter of 250 nm or less.

21. The hemostatic composition of claim 1 , wherein the hemostatic composition is a spray, aerosol, gel, or cement.

22. A medical device comprising:

a hemostatic composition of claim 1 ; and

a sterile substrate on which the hemostatic composition is disposed.

23. The device of claim 22 , wherein the substrate is adapted for delivery of the hemostatic composition to a bleeding wound.

24. The device of claim 23 , wherein the substrate is a sponge, gauze, bandage, swab, pillow or sleeve.

25. The device of claim 23 , further comprising a sealed package containing the hemostatic composition.

26. A method of promoting blood clotting at a hemorrhage site, comprising:

administering to a hemorrhage site in a subject the hemostatic composition of claim 1 for a period of time sufficient to at least initiate blood clotting at the hemorrhage site.

27. The method of claim 26 , wherein the hemorrhage site is an external hemorrhage site and the administering comprises applying the hemostatic composition to the external hemorrhage site.

28. The method of claim 26 , wherein the hemorrhage site is an internal hemorrhage site, and the hemostatic agent further comprises a protecting agent attached to the hemostatic agent by an enzymatically-cleavable linking group, and the administering comprises intravenously administering the hemostatic composition to the subject.

29. The hemostatic composition of claim 1 , wherein the nanoparticle is solid.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 13, 2015
From: KUDELA, DAMIEN; STUCKY, GALEN D.; MAY-MASNOU, ANNA; BRAUN, GARY BERNARD
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 037036/0883 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 13, 2015
From: MORRISSEY, JAMES H.; SMITH, STEPHANIE A.
To: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS
Reel/Frame 037036/0946 →
Continuity (3)
Continuation 14201434 · Mar 7, 2014
Provisional Application 61775354 · Mar 8, 2013
Related Publication 20160213809A1 · Jul 28, 2016
Cited By (1)
US 12,350,399