IP Library Granted Patent US 7,867,984
Granted Patent B1
US 7,867,984 · App. 12/459,657 · Granted Jan 11, 2011

Nanoparticles for protein drug delivery

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Quick Facts
Patent No.
US 7,867,984
App. No.
12/459,657
Granted
Jan 11, 2011
Kind
B1
Abstract

The invention discloses the bioactive nanoparticles composed of chitosan, poly-glutamic acid, and at least one appetite-suppressing agent characterized with a positive surface charge and a method of treating obesity in a subject in need via their enhanced permeability in oral drug delivery.

Claims (20)

1. A method of treating obesity in a subject in need thereof comprising identifying a subject in need of treatment for obesity and administering bioactive nanoparticles to said subject, wherein said nanoparticles consist of positively charged chitosan, a negatively charged substrate, and at least one appetite-suppressing agent, wherein a shell portion of said nanoparticles is dominated by said positively charged chitosan, and wherein said negatively charged substrate is at least partially neutralized with a portion of said positively charged chitosan in the core portion of said nanoparticles.

2. The method of claim 1 , wherein the chitosan has a molecular weight about 80 kDa or less.

3. The method of claim 1 , wherein said nanoparticles have a mean particle size between about 50 and 400 nanometers.

4. The method of claim 1 , wherein the chitosan is N-trimethyl chitosan, EDTA-chitosan, low molecular weight chitosan, chitosan derivatives or combinations thereof.

5. The method of claim 1 , wherein said nanoparticles are loaded in tablets or pills.

6. The method of claim 1 , wherein said nanoparticles are encapsulated in capsules.

7. The method of claim 6 , wherein said capsules further comprise at least a solubilizer or pharmacopoeial excipients.

8. The method of claim 6 , wherein said capsules are enterically coated.

9. The method of claim 6 , wherein said capsules further comprise at least one permeation enhancer.

10. The method of claim 9 , wherein said permeation enhancer is selected from the group consisting of Ca 2+ chelators, bile salts, anionic surfactants, medium-chain fatty acids, phosphate esters, chitosan, and chitosan derivatives.

11. The method of claim 1 , wherein said nanoparticles are freeze-dried, thereby said nanoparticles being in a powder form.

12. The method of claim 1 , wherein said nanoparticles are mixed with trehalose and then freeze-dried, thereby said nanoparticles being in a powder form.

13. The method of claim 1 , wherein said nanoparticles further comprise magnesium sulfate or TPP.

14. The method of claim 1 , wherein said at least one appetite-suppressing agent is appetite-suppressing peptide or peptide fraction.

15. The method of claim 1 , wherein said at least one appetite-suppressing agent is leptin.

16. The method of claim 1 , wherein said at least one appetite-suppressing agent is obestatin.

17. The method of claim 1 , wherein said at least one appetite-suppressing agent is ghrelin antagonist.

18. The method of claim 1 , wherein said at least one appetite-suppressing agent is Peptide YY.

19. The method of claim 1 , wherein said at least one appetite-suppressing agent is Urotensin-I or Urotensin II.

20. The method of claim 1 , wherein said at least one appetite-suppressing agent is cholecystokinin.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 7, 2016
From: GP MEDICAL, INC
To: NANOMEGA MEDICAL CORPORATION
Reel/Frame 038382/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 7, 2009
From: SUNG, HSING-WEN; TU, HOSHENG
To: GP MEDICAL, INC.
Reel/Frame 023070/0665 →