IP Library Granted Patent US 10,463,608
Granted Patent B2
US 10,463,608 · App. 15/350,718 · Granted Nov 5, 2019

Microneedle-based transdermal delivery system and method of making same

Inventor: Martin J. D'Souza (Duluth, GA)
Assignee: THE CORPORATION OF MERCER UNIVERSITY
A61K9/0021A61K9/1652A61K31/727A61K39/0008A61K39/0011A61K39/095A61K39/12A61K39/145A61K39/155A61K39/165A61K39/39A61M37/0015B29C33/42B29C39/023B29C41/003B29C41/04C12N5/0677C12N7/00C12N15/88A61K35/39A61K2039/5252A61K2039/54A61M2037/003A61M2037/0061B29K2029/04B29K2105/0035B29L2031/7544C12N2710/20023C12N2710/20034C12N2760/16034C12N2760/18534
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Quick Facts
Patent No.
US 10,463,608
App. No.
15/350,718
Granted
Nov 5, 2019
Kind
B2
Abstract

A transdermal delivery system of microneedles containing a bioactive material, comprising at least one layer of a support material; at least one biodegradable needle associated with the support material, each needle comprising at least one biodegradable polymer and at least one sugar, wherein each biodegradable needle is hollow and is adapted to retain a bioactive material.

Claims (46)

1. A transdermal delivery system, comprising:

at least one biodegradable needle comprising

i. at least one biodegradable polymer,

ii. at least one sugar; and,

iii. an encapsulated bioactive material,

wherein the at least one biodegradable needle contains encapsulated bioactive material such that the bioactive material does not directly contact the at least one biodegradable polymer or the at least one sugar.

2. A transdermal delivery system, comprising:

at least one biodegradable needle comprising

i. at least one biodegradable polymer, wherein the biodegradable polymer is polydimethylsiloxane;

ii. at least one sugar; and,

iii. an encapsulated bioactive material,

wherein the at least one biodegradable needle contains encapsulated bioactive material such that the bioactive material does not directly contact the at least one biodegradable polymer or the at least one sugar.

3. The system of claim 1 , wherein the sugar is at least one material selected from the group consisting of maltose and trehalose.

4. The system of claim 1 , wherein the bioactive material is at least one material selected from the group consisting of drugs, vaccines, and proteins, and mixtures thereof.

5. A transdermal delivery system, comprising:

at least one biodegradable needle comprising

i. at least one biodegradable polymer,

ii. at least one sugar; and,

iii. an encapsulated bioactive material,

wherein the at least one biodegradable needle contains encapsulated bioactive material such that the bioactive material does not directly contact the at least one biodegradable polymer or the at least one sugar; and,

wherein the bioactive material is at least one material provided in microencapsulated particle form.

6. A transdermal delivery system, comprising:

at least one biodegradable needle comprising

i. at least one biodegradable polymer;

ii. at least one sugar; and,

iii. an encapsulated bioactive material,

wherein the at least one biodegradable needle contains encapsulated bioactive material such that the bioactive material does not directly contact the at least one biodegradable polymer or the at least one sugar; and,

wherein the at least one biodegradable microneedle is able to degrade within 12 minutes after delivery to a subject's skin.

7. A transdermal delivery system, comprising:

at least one biodegradable needle comprising

i. at least one biodegradable polymer;

ii. at least one sugar; and,

iii. an encapsulated bioactive material,

wherein the at least one biodegradable needle contains encapsulated bioactive material such that the bioactive material does not directly contact the at least one biodegradable polymer or the at least one sugar; and,

wherein the bioactive material is in the form of microencapsulated material having an average particle size in a range of 0.01-50 μm.

8. A transdermal delivery system, comprising:

at least one biodegradable needle comprising

i. at least one biodegradable polymer;

ii. at least one sugar; and,

iii. an encapsulated bioactive material,

wherein the at least one biodegradable needle contains encapsulated bioactive material such that the bioactive material does not directly contact the at least one biodegradable polymer or the at least one sugar; and,

wherein the bioactive material is in the form of microencapsulated material having an average particle size in a range of 1-4 μm.

9. The system of claim 1 , further comprising an adjuvant.

10. The system of claim 1 , wherein the bioactive material is at least one material selected from the group consisting of a vaccine to gonorrhea, a vaccine to an antigen expressed by breast cancer cells, a vaccine to influenza, a vaccine to human papilloma virus, and a vaccine to respiratory syncytial virus.

11. The delivery system of claim 1 , wherein each biodegradable needle is solid.

12. The delivery system of claim 1 , wherein each biodegradable needle is hollow.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 27, 2017
From: D'SOUZA, MARTIN J.
To: THE CORPORATION OF MERCER UNIVERSITY
Reel/Frame 041378/0768 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 5, 2016
From: D'SOUZA, MARTIN J.
To: THE CORPORATION OF MERCER UNIVERSITY
Reel/Frame 040517/0843 →
Continuity (4)
Continuation In Part 14874978 · Oct 5, 2015
Continuation In Part 12569867 · Sep 29, 2009
Provisional Application 61100886 · Sep 29, 2008
Related Publication 20170157036A1 · Jun 8, 2017
Cited By (3)
US 12,186,515 US 12,636,250 US 12,714,838