IP Library Granted Patent US 9,095,521
Granted Patent B2
US 9,095,521 · App. 14/376,145 · Granted Aug 4, 2015

Methods for improving muscle strength

Inventors: Samuel A. Wickline (St. Louis, MO); Gregory M. Lanza (St. Louis, MO)
Assignee: Washington University
A61K9/51A61K9/0019A61K9/5115A61K9/5123A61K31/436
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Quick Facts
Patent No.
US 9,095,521
App. No.
14/376,145
Granted
Aug 4, 2015
Kind
B2
Abstract

The present invention relates to methods for improving muscle strength and treating muscular dystrophy.

Claims (20)

1. A method for increasing muscle strength in a subject, the method comprising administering rapamycin-loaded nanoparticles to a subject in need of increased muscle strength.

2. The method of claim 1 , wherein the subject has muscular dystrophy.

3. The method of claim 1 , wherein the subject is suffering from muscle weakness resulting from aging.

4. The method of claim 1 , wherein the subject is suffering from muscle weakness resulting from a traumatic injury or surgery.

5. The method for claim 1 , wherein the administration of rapamycin-loaded nanoparticles induces autophagy of muscle cells.

6. The method for claim 1 , wherein the administration of rapamycin-loaded nanoparticles attenuates muscle destruction.

7. The method for claim 1 , wherein the rapamycin-loaded nanoparticles are administered intravenously.

8. The method for claim 1 , wherein the rapamycin-loaded nanoparticles comprise between about 0.1 and 0.5% rapamycin.

9. The method for claim 1 , wherein the rapamycin-loaded nanoparticles are administered at least once a week.

10. The method for claim 1 , wherein 1 mL/kg of the rapamycin-loaded nanoparticles are administered at least once a week.

11. A method for attenuating muscle destruction in a subject, the method comprising administering rapamycin-loaded nanoparticles to a subject experiencing muscle destruction.

12. The method for claim 11 , wherein the administration of rapamycin-loaded nanoparticles induces autophagy.

13. The method for claim 11 , wherein the rapamycin-loaded nanoparticles are administered intravenously.

14. The method for claim 11 , wherein the rapamycin-loaded nanoparticles comprise between about 0.1 and 0.5% rapamycin.

15. The method for claim 11 , wherein the rapamycin-loaded nanoparticles are administered at least once a week.

16. A method for inducing autophagy in the muscle cells of a subject, the method comprising administering rapamycin-loaded nanoparticles so that autophagy is increased in the muscle cells of the subject.

17. The method for claim 16 , wherein the administration of rapamycin-loaded nanoparticles attenuates muscle destruction.

18. The method for claim 16 , wherein the rapamycin-loaded nanoparticles are administered intravenously.

19. The method for claim 16 , wherein the rapamycin-loaded nanoparticles comprise between about 0.1 and 0.5% rapamycin.

20. The method for claim 16 , wherein the rapamycin-loaded nanoparticles are administered at least once a week.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jul 11, 2016
From: WASHINGTON UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039301/0607 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2015
From: WICKLINE, SAMUEL; LANZA, GREGORY
To: WASHINGTON UNIVERSITY
Reel/Frame 034824/0401 →
Continuity (2)
Provisional Application 61594182 · Feb 2, 2012
Related Publication 20150011578A1 · Jan 8, 2015