IP Library Granted Patent US 7,550,439
Granted Patent B2
US 7,550,439 · App. 11/040,242 · Granted Jun 23, 2009

Methods for reducing oxidative damage

Assignee: Cornell Research Foundation, Inc.
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Quick Facts
Patent No.
US 7,550,439
App. No.
11/040,242
Granted
Jun 23, 2009
Kind
B2
Abstract

The invention provides a method for reducing oxidative damage in a mammal, a removed organ, or a cell in need thereof. The method comprises administering an effective amount of an aromatic cationic peptide. The aromatic cationic peptide has (a) at least one net positive charge; (b) a minimum of three amino acids; (c) a maximum of about twenty amino acids; (d) a relationship between the minimum number of net positive charges (p m ) and the total number of amino acid residues (r) wherein 3p m is the largest number that is less than or equal to r+1; (e) a relationship between the minimum number of aromatic groups (a) and the total number of net positive charges (p t ) wherein 3 a or 2 a is the largest number that is less than or equal to p t +1, except that when a is 1, p t may also be 1; and (f) at least one tyrosine or tryptophan amino acid.

Claims (24)

1. A method for reducing oxidative damage in a mammal in need thereof, the method comprising administering to the mammal an effective amount of D-Arg-Dmt-Lys-Phe-NH 2 peptide.

2. The method according to claim 1 , wherein the peptide is administered orally.

3. The method according to claim 1 , wherein the peptide is administered topically.

4. The method according to claim 1 , wherein the peptide is administered intranasally.

5. The method according to claim 1 , wherein the peptide is administered systemically.

6. The method according to claim 3 , wherein the peptide is administered intravenously.

7. The method according to claim 1 , wherein the peptide is administered subcutaneously.

8. The method according to claim 1 , wherein the peptide is administered intramuscularly.

9. The method according to claim 1 , wherein the peptide is administered intracerebroventricularly.

10. The method according to claim 1 , wherein the peptide is administered intrathecally.

11. The method according to claim 1 , wherein the peptide is administered transdermally.

12. The method according to claim 11 , wherein the transdermal administration is by iontophoresis.

13. The method according to claim 1 , wherein the mammal is undergoing reperfusion.

14. The method according to claim 13 , wherein the reperfusion is a treatment for ischemia.

15. The method according to claim 14 , wherein the ischemia is due to stroke.

16. The method according to claim 1 , wherein the mammal is suffering from sepsis.

17. The method according to claim 1 , wherein the mammal is suffering from an inflammatory process.

18. The method according to claim 17 , wherein the mammal is suffering from arthritis.

19. The method according to claim 1 , wherein the mammal is suffering from diabetes.

20. The method according to claim 1 , wherein the mammal is suffering from liver damage.

21. The method according to claim 20 , wherein the liver damage is caused by a viral infection.

22. The method according to claim 20 , wherein the liver damage is caused by a toxic agent.

23. The method according to claim 1 , wherein the mammal is a human.

24. A method of reducing oxidative damage in a removed organ of a mammal, the method comprising administering to the removed organ an effective amount of D-Arg-Dmt-Lys-Phe-NH 2 peptide.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2005
From: SZETO, HAZEL
To: CORNELL RESEARCH FOUNDATION, INC.
Reel/Frame 016534/0953 →
Continuity (2)
Provisional Application 6053884100 · Jan 23, 2004
Related Publication 20060084606A1 · Apr 20, 2006