US2010322875A1PendingUtilityA1
Silicone scar treatment preparation
Assignee: ADVANCED BIO TECHNOLOGIES INCPriority: Jun 18, 2009Filed: Jun 18, 2009Published: Dec 23, 2010
Est. expiryJun 18, 2029(~2.9 yrs left)· nominal 20-yr term from priority
Inventors:Paul Guilbaud
A61K 8/25A61K 31/618A61K 8/4973A61K 47/34A61Q 17/04A61K 8/35A61K 31/573A61L 26/0052A61K 2800/95A61K 9/0014A61K 2800/594A61K 8/345A61P 29/00A61K 8/895A61K 8/40A61L 26/0004A61K 47/24A61K 8/585A61K 31/695A61L 26/0066A61L 26/0095A61K 31/216A61K 8/37A61F 13/00A61P 17/02A61L 2300/41A61L 26/008A61K 47/02A61L 2430/34A61P 17/18A61K 8/891A61K 47/22A61L 26/0019A61K 2800/592A61K 31/12
67
PatentIndex Score
0
Cited by
0
References
0
Claims
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
exact text as granted — not AI-modified1 ) 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.Join the waitlist — get patent alerts
Track US2010322875A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.