IP Library Granted Patent US 9,326,995
Granted Patent B2
US 9,326,995 · App. 11/464,825 · Granted May 3, 2016

Oxides for wound healing and body repair

Inventors: Galen D. Stucky (Santa Barbara, CA); Todd A. Ostomel (Davis, CA); Qihui Shi (Goleta, CA); April Sawvel (Santa Barbara, CA); Sarah Baker (Pleasanton, CA)
Assignee: The Regents of the University of California
A61K33/00A61K33/06A61K33/24A61K33/26A61K33/30A61K33/42A61K45/06A61L24/02A61L26/0004
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Quick Facts
Patent No.
US 9,326,995
App. No.
11/464,825
Granted
May 3, 2016
Kind
B2
Abstract

The invention provides a homogeneous composition comprising a hemostatically effective amount of a charged oxide, wherein the composition has an isoelectric point, as measured in calcium chloride, below 7.3 or above 7.4. Typically, the charged oxide is selected from the group consisting of silaceous oxides, titanium oxides, aluminum oxides, calcium oxides, zinc oxides, nickel oxides and iron oxides. In some embodiments, the composition further comprises a second oxide selected from the group consisting of calcium oxide, sodium oxide, magnesium oxide, zinc oxide, phosphorus oxide and alumina. In a typical embodiment of the invention, the charged oxide is silaceous oxide, the second oxide comprises calcium oxide and the ratio, by molar ratio, of silaceous oxide to calcium oxide is 0.25 to 15. Optionally, the composition further comprises phosphorous oxide. Also described are methods of making and using such compositions.

Claims (14)

1. A device adapted for treatment of wounds comprising a hemostatic composition disposed as a coating on the device, the hemostatic composition comprising a hemostatically effective amount of kaolin hydrated from 0.1% to 25% and an inorganic salt, wherein the hemostatic composition has an isoelectric point, as measured in a calcium chloride solution, below the pH of blood, and wherein the hemostatic composition does not include a hemostatically effective amount of a zeolite.

2. The device of claim 1 , wherein the hemostatic composition has an isoelectric point below 7.3.

3. A method of modulating hemostasis, the method comprising contacting a wound with a device of claim 1 , wherein said contacting is sufficient to decrease blood coagulation time.

4. The device of claim 1 , wherein the hemostatic composition further comprises an oxide selected from the group consisting of calcium oxide, sodium oxide, magnesium oxide, zinc oxide, phosphorus oxide and alumina.

5. The device of claim 1 , wherein the inorganic salt comprises a divalent ion selected from the group consisting of zinc, copper, magnesium, calcium and nickel.

6. The device of claim 1 , wherein the inorganic salt is selected from the group consisting of: CaO, CaCl 2 , AgNO 3 , Ca(NO 3 ) 2 , Mg(NO 3 ) 2 , Zn(NO 3 ) 2 , NH 4 NO 3 , AgCl, Ag 2 O, zinc acetate, magnesium acetate, calcium citrate, zinc citrate, magnesium citrate, magnesium chloride, magnesium bromide, zinc chloride, zinc bromide, calcium bromide, calcium acetate and calcium phosphate.

7. A device adapted for treatment of wounds comprising a hemostatic composition disposed as a coating on the device, the hemostatic composition comprising a hemostatic agent and an inorganic salt, the hemostatic agent consisting essentially of a hemostatically effective amount of kaolin hydrated from 0.1% to 25%, wherein the hemostatic composition has an isoelectric point, as measured in a calcium chloride solution, below the pH of blood.

8. The device of claim 7 , wherein the hemostatic composition has an isoelectric point below 7.3.

9. A method of modulating hemostasis, the method comprising contacting a wound with a device of claim 7 , wherein said contacting is sufficient to decrease blood coagulation time.

10. The device of claim 7 , wherein the inorganic salt comprises a divalent ion selected from the group consisting of zinc, copper, magnesium, calcium and nickel.

11. The device of claim 7 , wherein the inorganic salt is selected from the group consisting of: CaCl 2 , AgNO 3 , Ca(NO 3 ) 2 , Mg(NO 3 ) 2 , Zn(NO 3 ) 2 , NH 4 NO 3 , AgCl, Ag 2 O, zinc acetate, magnesium acetate, calcium citrate, zinc citrate, magnesium citrate, magnesium chloride, magnesium bromide, zinc chloride, zinc bromide, calcium bromide, calcium acetate and calcium phosphate.

12. The device of claim 1 , wherein the hemostatic composition initiates detectable coagulation (R) in 2 minutes or less upon contacting the wound.

13. The device of claim 1 , wherein the hemostatic composition produces a rate of coagulation (α) of 50° or more upon contacting the wound.

14. The device of claim 1 , wherein the hemostatic composition produces a maximum clot strength (MA) of 55 mm to 100 mm upon contacting the wound.

Assignments (4)
CONFIRMATORY LICENSE Recorded Nov 18, 2013
From: CALIFORNIA, UNIVERSITY OF
To: NAVY, SECRETARY OF THE UNITED STATES OF AMERICA
Reel/Frame 031703/0057 →
CONFIRMATORY LICENSE Recorded May 23, 2013
From: CALIFORNIA, UNIVERSITY OF
To: NAVY, SECRETARY OF THE UNITED STATES OF AMERICA
Reel/Frame 030559/0634 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 21, 2009
From: STUCKY, GALEN D.; OSTOMEL, TODD A.; SHI, QIHUI; SAWVEL, APRIL; BAKER, SARAH
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 023403/0758 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 7, 2006
From: STUCKY, GALEN D.; OSTOMEL, TODD A.; SHI, QIHUI
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 018218/0351 →
Continuity (5)
Continuation In Part 11398161 · Apr 4, 2006
Provisional Application 60708206 · Aug 15, 2005
Provisional Application 60668022 · Apr 4, 2005
Related Publication 20070154564A1 · Jul 5, 2007
Related Publication 20100209531A2 · Aug 19, 2010