IP Library Granted Patent US 10,272,039
Granted Patent B2
US 10,272,039 · App. 15/525,557 · Granted Apr 30, 2019

Topical sodium nitrite formulation

Inventors: Haksong Jin (McLean, VA); George Grimes (Rockville, MD); Deborah Sperling (Woodbine, MD); Gopal Potti (Gaithersburg, MD); Caterina P. Minniti (Chevy Chase, MD); Gregory J. Kato (Woodbine, MD)
Assignee: The United States of America, as represented by the Secretary, Department of Health and Human Services
A61K9/06A61K9/0014A61K33/00A61K45/06A61K47/06
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Quick Facts
Patent No.
US 10,272,039
App. No.
15/525,557
Granted
Apr 30, 2019
Kind
B2
Abstract

A sodium nitrite formulation for topical administration is described. The formulation includes an aqueous solution of non-acidified sodium nitrite dispersed in a white petrolatum ointment. The concentration of sodium nitrite in the formulation is about 0.5% to about 3.0% by weight. To prepare the formulation, non-acidified sodium nitrite is completely dissolved in a small quantity of water, sterile filtered and dispersed in white petrolatum ointment.

Claims (12)

1. A non-acidified formulation for topical administration, comprising an aqueous solution of about 0.5% to about 3.0% by weight non-acidified sodium nitrite dispersed in a white petrolatum ointment, wherein the white petrolatum ointment comprises white petrolatum, mineral oil, ceresin, panthenol and bisabolol.

2. The formulation of claim 1 , wherein the white petrolatum ointment comprises a 41% petrolatum ointment.

3. The formulation of claim 1 , wherein the concentration of sodium nitrite is 0.5, 1.0, 1.5, 1.8, 2.0, 2.5 or 3.0% by weight.

4. A method of preparing the formulation of claim 1 , comprising:

dissolving sodium nitrite powder in water to produce an aqueous solution of sodium nitrite having a concentration of about 20% to about 40% sodium nitrite;

filtering the aqueous solution of sodium nitrite through a 0.22 micron filter; and

dispersing the filtered aqueous solution of nitrite into the white petrolatum ointment.

5. The method of claim 4 , wherein the concentration of the aqueous solution of sodium nitrite is about 30% sodium nitrite.

6. The method of claim 4 , wherein the volume of the aqueous solution dispersed into the white petrolatum ointment is about 4% to about 5% v/w.

7. The formulation of claim 1 , wherein the formulation has a pH of about 6.0-8.5.

8. A formulation for topical administration, comprising an aqueous solution of about 0.5% to about 3.0% by weight non-acidified sodium nitrite dispersed in a white petrolatum ointment, wherein the white petrolatum ointment comprises white petrolatum, mineral oil, ceresin, panthenol and bisabolol, and wherein the formulation does not comprise an acid or an acidifying agent.

9. A formulation for topical administration, consisting of an aqueous solution of about 0.5% to about 3.0% by weight non-acidified sodium nitrite dispersed in a white petrolatum ointment.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2017
From: KATO, GREGORY J.; MINNITI, CATERINA P.; JIN, HAKSONG; GRIMES, GEORGE; SPERLING, DEBORAH; POTTI, GOPAL
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Reel/Frame 042551/0830 →
Continuity (2)
Provisional Application 62077622 · Nov 10, 2014
Related Publication 20170333345A1 · Nov 23, 2017