IP Library Granted Patent US 9,675,637
Granted Patent B2
US 9,675,637 · App. 10/563,683 · Granted Jun 13, 2017

Use of nitrite salts for the treatment of cardiovascular conditions

Inventors: Mark T. Gladwin (Washington, DC); Alan N. Schechter (Bethesda, MD); David J. Lefer (Bronx, NY); Rakesh P. Patel (Birmingham, AL); Christian J. Hunter (Boston, MA); Gordon G. Power (Redlands, CA); Daniel B. Kim-Shapiro (Winston-Salem, NC); Ryszard Pluta (Bethesda, MD); Edward H. Oldfield (Philomont, VA); Richard O. Cannon, III (Potomac, MD)
Assignees: The United States of America as represented by the Secretary of the Department of Health and Human Services; The Board of Supervisors of Louisiana State University and Agricultural and Mechanical College, acting through Louisiana State University Health Sciences Center; The UAB Research Foundation; Loma Linda University; Wake Forest University
A61K33/00A61K45/06
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Quick Facts
Patent No.
US 9,675,637
App. No.
10/563,683
Granted
Jun 13, 2017
Kind
B2
Abstract

It has been surprisingly discovered that administration of nitrite to subjects causes a reduction in blood pressure and an increase in blood flow to tissues. The effect is particularly beneficial, for example, to tissues in regions of low oxygen tension. This discovery provides useful treatments to regulate a subject's blood pressure and blood flow, for example, by the administration of nitrite salts. Provided herein are methods of administering a pharmaceutically-acceptable nitrite salt to a subject, for treating, preventing or ameliorating a condition selected from: (a) ischemia-reperfusion injury (e.g., hepatic or cardiac or brain ischemia-reperfusion injury); (b) pulmonary hypertension (e.g., neonatal pulmonary hypertension); or (c) cerebral artery vasospasm.

Claims (20)

1. A method for treating or ameliorating a condition selected from:

(a) hepatic or cardiac or brain ischemia-reperfusion injury;

(b) pulmonary hypertension; or

(c) cerebral artery vasospasm,

in a subject by decreasing blood pressure and/or increasing vasodilation in the subject, the method comprising administering a therapeutically effective amount of non-acidified sodium nitrite to the subject to decrease the blood pressure and/or increase vasodilation in the subject, wherein the sodium nitrite is administered to a circulating concentration of about 0.6 to 240 μM, and wherein the administration is by a route whereby the non-acidified sodium nitrite contacts blood in the subject, and the route is selected from the group consisting of intravenous, intramuscular, rectal, ex vivo, intraocular, intraperitoneal, intraarterial, subcutaneous, inhalation, and into a cardiopulmonary bypass circuit, thereby treating or ameliorating the condition.

2. The method of claim 1 , which is a method for treating or ameliorating hepatic or cardiac or brain ischemia-reperfusion injury.

3. The method of claim 2 , wherein administering sodium nitrite to the subject is intravenous.

4. The method of claim 1 , which is a method for treating or ameliorating pulmonary hypertension.

5. The method of claim 4 , wherein the pulmonary hypertension is neonatal pulmonary hypertension.

6. The method of claim 4 , wherein administering sodium nitrite to the subject is by inhalation.

7. The method of claim 6 , wherein the sodium nitrite is nebulized.

8. The method of claim 4 , wherein the sodium nitrite is administered at a rate of 270 μmol/minute.

9. The method of claim 1 , which is a method for treating or ameliorating cerebral artery vasospasm.

10. The method of claim 9 , wherein administering sodium nitrite to the subject is intravenous.

11. The method of claim 9 , wherein the sodium nitrite is administered at a rate of about 45 to 60 mg/kg.

12. The method of claim 1 , wherein the sodium nitrite is administered in combination with at least one additional agent.

13. The method of claim 1 , wherein the subject is a mammal.

14. The method of claim 13 , wherein the subject is a human.

15. The method of claim 1 , wherein the non-acidified sodium nitrite is administered to the subject in an amount and for a sufficient period of time to reach a circulating concentration in blood of the subject of no more than about 20 μM, thereby treating or ameliorating the condition.

16. The method of claim 1 , wherein the non-acidified sodium nitrite is administered to the subject in an amount and for a sufficient period of time to reach a circulating concentration in blood of the subject of no more than about 16 μM, thereby treating or ameliorating the condition.

Assignments (7)
CONFIRMATORY LICENSE Recorded Aug 27, 2021
From: UNIVERSITY OF ALABAMA AT BIRMINGHAM
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 057337/0971 →
CHANGE OF NAME Recorded Nov 17, 2010
From: PATEL, RAKESH P.
To: THE UAB RESEARCH FOUNDATION
Reel/Frame 025382/0842 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 17, 2006
From: HUNTER, CHRISTIAN J.
To: THE GOVERNMENT OF THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE DEPARTMENT OF HEALTH AND HUMAN SERVICES
Reel/Frame 018644/0515 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2006
From: GLADWIN, MARK T.; SCHECHTER, ALAN N.; PLUTA, RYSZARD; OLDFIELD, EDWARD H.; CANNON, RICHARD O., III
To: THE GOVERNMENT OF THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE DEPARTMENT OF HEALTH AND HUMAN SERVICES
Reel/Frame 018580/0077 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2006
From: POWER, GORDON G.
To: LOMA LINDA UNIVERSITY
Reel/Frame 018462/0726 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2006
From: KIM-SHAPIRO, DANIEL B.
To: WAKE FOREST UNIVERSITY
Reel/Frame 018462/0723 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2006
From: PATEL, RAKESH P.
To: THE UNIVERSITY OF ALABAMA RESEARCH FOUNDATION
Reel/Frame 018462/0870 →
Continuity (3)
Provisional Application 60485959 · Jul 9, 2003
Provisional Application 60511244 · Oct 14, 2003
Related Publication 20070154569A1 · Jul 5, 2007