IP Library Granted Patent US 9,393,283
Granted Patent B2
US 9,393,283 · App. 13/916,882 · Granted Jul 19, 2016

Povidone-iodine topical composition

Inventor: Griscom Bettle, III (Sarasota, FL)
Assignee: Microdemis Corporation
A61K36/889A61K9/0014A61K31/165A61K31/4015A61K33/18A61K35/644
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Quick Facts
Patent No.
US 9,393,283
App. No.
13/916,882
Granted
Jul 19, 2016
Kind
B2
Abstract

The present invention relates to a topical pharmaceutical composition comprising povidone-iodine, a tertiary amide, surfactant and coconut oil, useful for killing microbes and treating wounds or sores on the surface of the skin.

Claims (41)

1. A method for treating a wound or open sore on a subject which comprises

placing a microbicidal effective amount of a topical pharmaceutical composition onto the wound or open sore and rubbing the composition thereon thoroughly,

said composition comprising:

an antiseptic effective amount of povidone-iodine complex wherein the amount of complexed iodine in the povidone-iodine complex is from about 4% to about 12% by weight of the povidone-iodine complex;

a second component comprising a tertiary amide or a salt thereof or a hydrate thereof, said second component present in an amount from about 0.1% to about 2% by weight of the composition;

coconut oil in an amount from about 0.5% to about 2% by weight of the composition;

an emulsifying effective amount of a surfactant; and

water;

said composition having a pH of about 2.0 to about 3.5 and having a specific gravity from about 0.9 to about 1.1; and

said composition containing less than 5% by weight of an ingredient that reacts with iodine.

2. The method according to claim 1 , wherein the povidone-iodine complex is present in an amount from about 5% to about 10% by weight of the composition.

3. The method according to claim 1 , wherein the surfactant is a polyethylene glycol of 4-(1,1,3,3-tetramethylbutyl)-phenyl, or Nonoxynol 9, or combination thereof.

4. The method according to claim 3 , wherein the povidone-iodine complex is present in an amount from about 5% to about 10% by weight of the composition.

5. The method according to claim 1 , wherein the composition further comprises beeswax.

6. The method according to claim 1 , wherein the tertiary amide has the formula

wherein R 4 is a saturated fatty group of 11-29 carbon atoms;

R 5 and R 6 are independently lower alkyl aryl, aryl lower alkyl, or saturated fatty group containing 11-29 carbon atoms or R 7 :

R 7 is

R 1 —Ar—O—R 2 —O—R 3 —;

R 2 and R 3 are independently alkylene groups containing 1-6 carbon atoms,

R 1 is a lower alkyl, and

Ar is aryl.

7. The method according to claim 6 , wherein R 4 is a saturated fatty group containing 15-21 carbon atoms.

8. The method according to claim 6 , wherein R 5 is aryl or aryl lower alkyl; and R 6 is

R 1 —Ar—O—R 2 —O—R 3 —;

R 2 and R 3 are independently alkylene containing 1-3 carbon atoms; and Ar is aryl.

9. The method according to claim 6 , wherein Ar is phenyl.

10. The method according to claim 6 , wherein R 5 is aryl lower alkyl.

11. The method according to claim 6 , wherein R 5 is benzyl.

12. The method according to claim 11 , wherein R 4 is a saturated fatty group containing 15-21 carbon atoms.

13. The method according to claim 6 , wherein the tertiary amide is benzethonium stearamide or benzalkonium stearamide.

14. The method according to claim 1 , wherein the second component comprises a hydrate of a tertiary amide, wherein the tertiary amide is of the formula

R 4 is a saturated fatty group of 11-29 carbon atoms;

R 5 and R 6 are independently lower alkyl, aryl, aryl lower alkyl, or fatty group containing 11-29 carbon atoms or R 7 ;

R 7 is

R 1 —Ar—O—R 2 —O—R 3 —;

R 2 and R 3 are independently alkylene groups containing 1-6 carbon atoms;

R 1 is an alkyl group containing 1-15 carbon atoms; and

Ar is aryl.

15. The method according to claim 1 , wherein the composition is in the form of a paste, cream or ointment.

16. The method according to claim 1 , wherein the composition is in the form of an aerosol spray.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 8, 2019
From: MICRODERMIS CORPORATION
To: HOSLER, JAMES P.
Reel/Frame 050005/0815 →
SECURITY INTEREST Recorded Jan 5, 2017
From: MICRODERMIS CORPORATION
To: HOSLER, JAMES, DR.
Reel/Frame 040862/0683 →
SECURITY INTEREST Recorded Dec 2, 2015
From: MICRODERMIS CORPORATION
To: CLARK, MICHAEL R.
Reel/Frame 037193/0445 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 4, 2015
From: BETTLE, GRISCOM, III
To: DRSS GLOBAL, LLC
Reel/Frame 036495/0001 →
CHANGE OF NAME Recorded Sep 4, 2015
From: DRSS GLOBAL, LLC
To: MICRODERMIS CORPORATION
Reel/Frame 036554/0781 →
Continuity (3)
Continuation 13696385
Provisional Application 61332417 · May 7, 2010
Related Publication 20140093583A1 · Apr 3, 2014