IP Library Granted Patent US 8,865,206
Granted Patent B1
US 8,865,206 · App. 14/102,027 · Granted Oct 21, 2014

Surface modified multilayered nanostructures for dermal delivery

Inventors: Mandip Sachdeva (Tallahassee, FL); Punit Shah (Tallahassee, FL)
Assignee: Florida A&M University
A61K9/0014A61K38/08A61K9/5123A61K9/5153A61K9/5161A61K31/192Y10S977/706Y10S977/737Y10S977/74Y10S977/906
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Quick Facts
Patent No.
US 8,865,206
App. No.
14/102,027
Granted
Oct 21, 2014
Kind
B1
Abstract

Dermal delivery is best suited for the various skin diseases or disorders. However, the stratum corneum limits the permeation of number of suitable pharmaceutical agents for dermal delivery. Certain embodiments of the present invention include surface modified multilayered nanostructures. The modification was completed by using fatty acids enabling delivery of a significant amount of one or more pharmaceutical agent(s) into deeper layers of the epidermis and dermis to treat skin diseases or disorders. Each active pharmaceutical agent can be encapsulated into the separate layers of the nanostructures.

Claims (26)

1. A composition for dermal delivery of at least one pharmaceutical agent through a stratum corneum of a subject, comprising each of the at least one a pharmaceutical agent admixed with at least one layer of polymeric nanostructures, wherein the at a least one layer of polymeric nanostructures includes an outer layer with an outer surface covalently bonded by at least one spacer linked to at least one skin-permeating fatty acid such that the at least one spacer linked to the at least one skin-permeating fatty acid extends from the outer surface of the outer layer of polymeric nanostructures to facilitate penetration of the composition through the stratum corneum of the subject, wherein the at least one spacer linked to the at least one fatty acid is a fatty acid-PEG-succinimidyl glutamate ester structure.

2. The composition of claim 1 , wherein the fatty acid is oleic acid.

3. The composition of claim 1 , wherein the at least one pharmaceutical agent is selected from the group consisting of spantide II, cyclosporine A, alpha-MSH, capsaicin and ketoprofen.

4. The composition of claim 1 , further comprising at least one polymer.

5. The composition of claim 4 , wherein the at least one polymer is PLGA.

6. The composition of claim 1 , further comprising at least one lipid or polymer.

7. The composition of claim 6 , wherein the at least one lipid is a derivative of glycerol.

8. The composition of claim 1 , further comprising an emulsifying agent.

9. The composition of claim 8 , wherein the emulsifying agent is polyvinyl alcohol.

10. The composition of claim 1 , further comprising a surfactant.

11. The composition of claim 10 , wherein the surfactant is polyoxyethylene (20) sorbitan monooleate.

12. The composition of claim 1 , further comprising an anti-foaming agent.

13. The composition of claim 12 , wherein the anti-foaming agent is sorbitan monooleate.

14. The composition of claim 1 , further comprising a cross-linking agent.

15. The composition of claim 14 , wherein the cross-linking agent is selected from the group consisting of sodium tripolyphosphate and glutaraldehyde.

16. A carrier for dermal delivery of at least one pharmaceutical agent through a stratum corneum of a subject, comprising each of the at least one a pharmaceutical agent and at least one layer of polymeric nanostructures, wherein the at least one layer of polymeric nanostructures includes an outer layer with an outer surface covalently bonded by at least one spacer linked to at least one skin-permeating fatty acid such that the at least one spacer linked to the at least one skin-permeating fatty acid extends from the outer surface a of the outer layer of polymeric nanostructures to facilitate penetration of the composition through the stratum corneum, admixed with a carrier agent, whereby the carrier is formulated wherein the at least one spacer linked to the at least one fatty acid is a fatty acid-PEG-succinimidyl glutamate ester structure.

17. The carrier of claim 16 , wherein the formulated carrier is selected from the group consisting of aqueous dispersions, nanogels, lotions, powders, emulsion, liniments, ointments, creams and patches.

18. A composition for dermal delivery of at least one pharmaceutical agent, comprising:

the at least one pharmaceutical agent;

a layer of nanostructures having a formula of formula I

at least one polymer, wherein the at least one polymer is PLGA;

at least one lipid, wherein the at least one lipid is 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE);

an emulsifying agent, wherein the emulsifying agent is polyvinyl alcohol;

a surfactant, wherein the surfactant is polyoxyethylene (20) sorbitan monooleate;

an anti-foaming agent, wherein the anti-foaming agent is sorbitan monooleate; and

a cross-linking agent, wherein the cross-linking agent is sodium tripolyphosphate.

Assignments (2)
CONFIRMATORY LICENSE Recorded May 20, 2015
From: FLORIDA AGRICULTURAL AND MECHANICAL UNIV
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 035741/0337 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2013
From: SACHDEVA, MANDIP; SHAH, PUNIT
To: FLORIDA A&M UNIVERSITY
Reel/Frame 031811/0436 →
Continuity (2)
Continuation 13289733 · Nov 4, 2011
Provisional Application 61410547 · Nov 5, 2010