IP Library Patent Application 12487489
Patent Application
App. No. 12/487,489

SILICONE SCAR TREATMENT PREPARATION

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Patent No.
US None
App. No.
12/487,489
Abstract

Disclosed is 1) a method for greatly increasing the solubility of useful actives in siloxane matrix-forming preparations, and 2) the associated preparations, themselves. Volatilizing coagents are utilized to give novel gels containing heretofore siloxane-insoluble additives.

Claims (35)

1 ) A spreadable preparation for aiding in the healing of wounds, as well as improving the characteristics of the post-epithelialially developed tissue at the wound site, said preparation comprising:

a) a volatile component;

b) siloxane matrix precursors; wherein said precursors are capable of forming a siloxane matrix at temperatures in the range of from about 95 to 100 degrees Fahrenheit during evaporation of the volatile component;

c) an active component having low miscibility and low solubility in said siloxane matrix precursors;

d) a volatile coagent;

wherein said volatile coagent is capable of forming a complex with said active component to form a solubilized active component; wherein the complex is miscible in said siloxane matrix precursors; and wherein all or a portion of said volatile coagent evaporates from the preparation upon the formation of the siloxane matrix.

2 ) The spreadable preparation as in claim 1 wherein the volatile coagent is an ester of a linear acid having a carbon chain length in the range of from about 6 to 13 carbon atoms and methanol, ethanol, or a secondary alcohol having a total carbon content in the range of from about 3 to about 8 carbon atoms.

3 ) The spreadable preparation as in claim 1 wherein the volatile coagent is a glycol comprised of a linear chain of three or more carbons and one or more hydroxyl groups; and wherein all hydroxyl groups are on adjacent carbons including an end carbon.

4 ) The spreadable preparation as in claim 1 wherein the volatile coagent is a substituted or unsubstituted isosorbide.

5 ) The spreadable preparation as in claim 1 wherein the active component comprises an agent having sun screening activity.

6 ) The spreadable preparation as in claim 1 wherein the active component comprises an agent having antihistamine or pain relieving activity.

7 ) The spreadable preparation as in claim 5 wherein the active component comprises one or more of the following: Octocrylene (ISP Escalol 597), Octinoxate (ISP Escalol 557), Octisalate (ISP Escalol 587), or Oxybenzone (ISP Escalol 567).

8 ) The spreadable preparation as in claim 6 wherein the active component comprises Hydrocortisone Acetate USP.

9 ) The spreadable preparation as in claim 1 wherein the volatile coagent comprises Dimethyl isosorbide

10 ) The spreadable preparation as in claim 1 wherein the volatile coagent comprises isopropyl myristate.

11 ) The spreadable preparation as in claim 1 wherein the volatile coagent comprises pentylene glycol.

12 ) The spreadable preparation as in claim 6 wherein the volatile coagent comprises isopropyl myristate.

13 ) The spreadable preparation as in claim 8 wherein the volatile coagent comprises Dimethyl isosorbide

14 ) The spreadable preparation as in claim 13 wherein the volatile coagent comprises pentylene glycol.

15 ) The spreadable preparation as in claim 1 wherein the siloxane matrix precursors comprise dimethicone crosspolymer, fumed silica, and dimethicone.

16 ) A method as in claim 1 wherein the volatile component is cyclopentasiloxane.

17 ) A method for the preparation of a spreadable preparation for aiding in the healing of wounds and the development of scar tissue, said preparation comprising:

a) a volatile component;

b) siloxane matrix precursors; wherein said precursors are capable of forming a siloxane matrix at temperatures in the range of from about 95 to 100 degrees Fahrenheit during evaporation of the volatile component;

c) an active component having low miscibility and low solubility in said siloxane matrix precursors;

d) a volatile coagent;

wherein said volatile coagent is capable of forming a complex with said active component to form a solubilized active component; wherein the complex is miscible in said siloxane matrix precursors; and wherein all or a portion of said volatile coagent evaporates from the preparation upon the formation of the siloxane matrix.

said method comprising the steps of:

a) providing said active component

b) providing said volatile coagent

c) providing siloxane matrix precursors

d) forming a complex between the volatile coagent and said active component which is miscible.

18 ) The method of claim 17 wherein the siloxane matrix precursors comprise dimethicone crosspolymer, fumed silica, and dimethicone and the volatile component comprises cyclopentasiloxane.

19 ) The method of claim 17 wherein the volatile coagent comprises isopropyl myristate and the active component comprises one or more of the following: Octocrylene (ISP Escalol 597), Octinoxate (ISP Escalol 557), Octisalate (ISP Escalol 587), or Oxybenzone (ISP Escalol 567).

20 ) The method of claim 17 wherein the volatile coagent comprises pentylene glycol and/or dimethyl isosorbide and the active component comprises Hydrocortisone Acetate.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Jun 10, 2025
From: BANK OF SCOTLAND PLC
To: ADVANCED BIO-TECHNOLOGIES, INC.
Reel/Frame 071374/0859 →
SECURITY INTEREST Recorded Mar 4, 2016
From: ADVANCED BIO-TECHNOLOGIES, INC.
To: BANK OF SCOTLAND PLC
Reel/Frame 037894/0237 →
SECURITY AGREEMENT Recorded Dec 15, 2011
From: ADVANCED BIO-TECHNOLOGIES, INC.
To: CLYDESDALE BANK PLC
Reel/Frame 027389/0115 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 16, 2010
From: GUILBAUD, PAUL
To: ADVANCED BIO-TECHNOLOGIES, INC.
Reel/Frame 024700/0651 →