IP Library Granted Patent US 8,865,696
Granted Patent B2
US 8,865,696 · App. 13/924,211 · Granted Oct 21, 2014

Morphine and morphine precursors

Inventors: George B. Stefano (Melville, NY); Patrick Cadet (Elmont, NY); Kirk J. Mantione (Patchogue, NY); Wei Zhu (West Babylon, NY)
Assignee: The Research Foundation for the State University of New York
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Quick Facts
Patent No.
US 8,865,696
App. No.
13/924,211
Granted
Oct 21, 2014
Kind
B2
Abstract

Methods and materials related to the use of morphine, morphine precursors (e.g., reticuline), and inhibitors of morphine synthesis or activity to treat diseases, to reduce inflammation, or to restore normal function are provided.

Claims (16)

1. A method for inducing nitric oxide release from cells in a mammal, said method comprising administering, to said mammal, a composition in an amount, at a frequency more frequent than once a week, and for a duration longer than one month, wherein said composition comprises one or more agents selected from the group consisting of reticuline, norlaudanosoline, and salutaridine, and wherein said amount of said composition results in less than 1 mg of said one or more agents being administered to said mammal per kg of body weight of said mammal per day.

2. The method of claim 1 , wherein said cells are immune cells.

3. The method of claim 1 , wherein said mammal is a human.

4. The method of claim 1 , wherein said composition further comprises morphine in an amount that results in less than 0.05 mg of said morphine being administered to said mammal per kg of body weight of said mammal per day.

5. The method of claim 1 , wherein said composition is in the form of a tablet.

6. The method of claim 1 , wherein said composition comprises selenium.

7. The method of claim 1 , wherein said composition comprises L-arginine.

8. The method of claim 1 , wherein said composition comprises a calcium source.

9. The method of claim 1 , wherein said amount of said composition results in less than 0.5 mg of said one or more agents being administered to said mammal per kg of body weight of said mammal per day.

10. The method of claim 1 , wherein said amount of said composition results in less than 0.05 mg of said one or more agents being administered to said mammal per kg of body weight of said mammal per day.

11. The method of claim 1 , wherein said frequency is more frequent than four times a week.

12. The method of claim 1 , wherein said frequency is between two and five times a day.

13. The method of claim 1 , wherein said frequency is once a day.

14. The method of claim 1 , wherein said duration is longer than two months.

15. The method of claim 1 , wherein said duration is longer than three months.

16. The method of claim 1 , wherein said composition comprises reticuline, norlaudanosoline, and salutaridine.

Assignments (3)
CHANGE OF NAME Recorded Aug 14, 2014
From: THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK
To: THE RESEARCH FOUNDATION FOR THE STATE UNIVERSITY OF NEW YORK
Reel/Frame 033535/0564 →
CONFIRMATORY LICENSE Recorded Sep 3, 2013
From: THE RESEARCH FOUNDATION FOR THE STATE UNIVERSITY OF NEW YORK
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 031140/0363 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 5, 2013
From: STEFANO, GEORGE B.; CADET, PATRICK; MANTIONE, KIRK J.; ZHU, WEI
To: THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK
Reel/Frame 030944/0364 →
Continuity (5)
Continuation 12904373 · Oct 14, 2010
Continuation 11576448
Provisional Application 60714769 · Sep 6, 2005
Provisional Application 60615048 · Oct 1, 2004
Related Publication 20130309326A1 · Nov 21, 2013