IP Library Granted Patent US 8,968,790
Granted Patent B2
US 8,968,790 · App. 13/706,755 · Granted Mar 3, 2015

Nanoformulation of vitamin D derivatives and/or vitamin D metabolites

Inventor: Shaker A. Mousa (Wynantskill, NY)
A61K9/5161A61K47/48038A61K47/4823Y10S977/773Y10S977/906B82Y5/00
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Quick Facts
Patent No.
US 8,968,790
App. No.
13/706,755
Granted
Mar 3, 2015
Kind
B2
Abstract

A nanoformulation that includes loaded nanoparticles. Each nanoparticle includes a modified chitosan polymer encapsulating at least one vitamin D derivative, at least one vitamin D metabolite, or combinations thereof. The modified chitosan polymer includes chitosan covalently linked to at least one entity selected from the group consisting of fatty acids (omega-3-fattay acids), amino acids, deoxycholic acid, alginate, arginine-alginate, hyaluronic acid, collagen, collagen-hydroxyapatite, poly(lactic-co-glycolic acid) (PLGA), and combinations thereof. A structure includes a medium and the nanoformulation, wherein the nanoparticles are dispersed in the medium. A method of using the nanoformulation to treat a disorder and improve efficacy of current therapies where resistance develop in a patient includes administering to the patient a therapeutically effective amount of the nanoformulation for treating the disorder. A nano-cosmetic formulation, comprising a cosmetic includes the nanoformulation, wherein the modified chitosan polymer encapsulates the at least one vitamin D derivative, and wherein the at least one vitamin D derivative encompasses 0.1 to 20.0 wt % of the nano-cosmetic formulation's total weight.

Claims (34)

1. A nanoformulation, comprising:

nanoparticles, each nanoparticle comprising a modified chitosan polymer encapsulating at least one vitamin D derivative, at least one vitamin D metabolite, or combinations thereof,

wherein the modified chitosan polymer comprises chitosan covalently linked to at least one entity selected from the group consisting of fatty acids, amino acids, deoxycholate, alginate, arginine-alginate, collagen, collagen-hydroxyapatite, poly(lactic-co-glycolic acid) (PLGA), and combinations thereof,

wherein the modified chitosan polymer is hydrophobic, and wherein the chitosan comprises a molecular weight in a range of 5 to 150 kilo Daltons.

2. The nanoformulation of claim 1 , wherein the modified chitosan polymer comprises chitosan covalently linked to the fatty acids, and wherein the fatty acids are selected from the group consisting of eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), linolenic acid, hyaluronic acid, and combinations thereof.

3. The nanoformulation of claim 1 , wherein the modified chitosan polymer encapsulates the at least one vitamin D derivative, and wherein the at least one vitamin D derivative is selected from the group consisting of vitamin D1 (ergocalciferol with lumisterol in a 1:1 ratio), vitamin D2 (ergocalciferol), D3 (cholecalciferol), D4 (22-dihydroergocalciferol), D5 (sitocalciferol), pre-vitamin D2, pre-vitamin D3, ergosterol, 7-dehydrocholesterol, lumisterol, pyrocalciferol, isopyrocalciferol, tachysterol, calcipotriene, calcitriol, and combination thereof.

4. The nanoformulation of claim 1 , wherein the modified chitosan polymer encapsulates the at least one vitamin D metabolite, and wherein the at least one vitamin D metabolite is selected from the group consisting of 25 hydroxyvitamin D, (1, 25 hydroxyvitamin D), and combinations thereof.

5. The nanoformulation of claim 1 , wherein the chitosan is covalently linked to the at least one entity by a respective cleavable linker, and wherein the respective cleavable linker cleavably links a NH 2 group or a CH 2 OH group in the chitosan to an entity of the at least one entity.

6. The nanoformulation of claim 1 , wherein the nanoformulation is configured to be applied topically or delivered orally to a mammal.

7. The nanoformulation of claim 6 , wherein the modified chitosan polymer has muco-adhesive properties with respect to the mammal.

8. The nanoformulation of claim 1 , wherein the modified chitosan polymer encapsulates at least one antioxidant selected from the group consisting of a polyphenol, an isoflavone, a flavone, and combinations thereof.

9. A structure, comprising:

a medium; and

the nanoformulation of claim 1 , wherein the nanoparticles are dispersed in the medium.

10. The structure of claim 9 , wherein the medium is selected from the group consisting of polyethylene glycol (PEG), poly oxy ethylene-glyceryl-tri-fatty acids (POEG), water resistant thin film forming cellulose polymer bridged by ethyl or ethoxy ether linkage, and silicone gel.

11. The structure of claim 10 , wherein the modified chitosan polymer encapsulates at least one vitamin D derivative, and wherein the at least one vitamin D derivative has a concentration of 0.01-10 mg/ml in the medium.

12. The structure of claim 9 , wherein the medium is selected from the group consisting of a tablet, a capsule, and an emulsion, wherein the modified chitosan polymer encapsulates at least one vitamin D derivative, and wherein the at least one vitamin D derivative has a concentration of 0.01-10 mg/ml in the medium.

13. The structure of claim 9 , wherein the nanoparticles are selected from the group consisting of eicosapentaenoic acid (EPA) nanoparticles, docosahexaenoic acid (DHA) nanoparticles, chitosan-deoxycholate nanoparticles, chitosan-alginate nanoparticles, chitosan-arginine-alginate nanoparticles, chitosan-linolenic acid nanoparticles, chitosan-hyaluronic acid nanoparticles, chitosan-collagen-hydroxyapatite nanoparticles, chitosan-poly(lactic-co-glycolic acid) (PLGA) nanoparticles, and combinations thereof.

14. A method of treating a disorder in a patient, said method comprising:

administering to the patient a therapeutically effective amount of the nanoformulation of claim 1 for treating the disorder.

15. The method of claim 14 , wherein the disorder, is selected from the group consisting of osteoporosis, skin aging, psoriasis, a vascular disorder, cardiovascular, cancer, and infectious disorders.

16. The method of claim 14 , wherein said administering comprises applying the nanoformulation topically to the patient or delivering the nanoformulation orally to the patient.

17. A nano-cosmetic formulation, comprising a cosmetic that includes the nanoformulation of claim 1 , wherein the modified chitosan polymer encapsulates at least one vitamin D derivative, and wherein the at least one vitamin D derivative encompasses 0.1 to 20.0 wt % of the total weight of the nano-cosmetic formulation.

18. Thenano-cosmetic formulation of claim 17 , wherein the cosmetic is in a form of cream, ointment, shampoo, or rinse.

19. A method of treating a patient for a disorder, said method comprising:

administering the nanoformulation of claim 1 systemically to the patient to counteract resistance developed by the patient to the therapy.

20. The method of claim 19 , wherein the disorder is selected from the group consisting of cancer, viral infection, hepatitis B, hepatitis C, diabetes, and combinations thereof.

21. The nanoformulation of claim 1 , wherein the modified chitosan polymer comprises chitosan covalently linked to the amino acids.

22. The nanoformulation of claim 1 , wherein the modified chitosan polymer comprises chitosan covalently linked to the deoxycholate.

23. The nanoformulation of claim 1 , wherein the modified chitosan polymer comprises chitosan covalently linked to the alginate.

24. The nanoformulation of claim 1 , wherein the modified chitosan polymer comprises chitosan covalently linked to the arginine-alginate.

25. The nanoformulation of claim 1 , wherein the modified chitosan polymer comprises chitosan covalently linked to the collagen.

26. The nanoformulation of claim 1 , wherein the modified chitosan polymer comprises chitosan covalently linked to the collagen-hydroxyapatite.

27. The nanoformulation of claim 1 , wherein the modified chitosan polymer comprises chitosan covalently linked to the PLGA.

Continuity (2)
Provisional Application 61568674 · Dec 9, 2011
Related Publication 20130149385A1 · Jun 13, 2013