US2010292139A1PendingUtilityA1
Topical drug delivery using phosphatidylcholine
Est. expiryMay 31, 2022(expired)· nominal 20-yr term from priority
Inventors:Nicholas V. Perricone
A61P 3/10A61P 5/06A61K 38/27A61K 38/23A61K 9/02A61K 9/1277A61K 47/24A61K 31/56A61K 38/24A61K 47/14A61P 17/00A61K 38/31A61K 38/095A61K 38/02A61K 38/56A61K 9/127A61K 38/28A61K 9/06A61K 47/10A61K 47/34A61K 47/22C07K 14/62A61K 9/0014A61J 3/07
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Claims
Abstract
The present invention relates to compositions and methods for transdermal drug delivery comprising formulating a phosphatidylcholine carrier composition containing the drug and applying the composition to the skin.
Claims
exact text as granted — not AI-modified1 . A composition comprising crystallized phosphatidylcholine and molecules entrapped within said phosphatidylcholine.
2 . A composition of claim 1 , wherein the molecules comprise polypeptides.
3 . The composition of claim 1 wherein the molecules are selected from the group consisting of oxytocin, vasopressin, insulin, somatotropin, calcitonin, chorionic gonadotropin, menotropins, follitropins, somatostatins, progestins, and combinations of any of these.
4 . The composition of claim 1 wherein the composition contains about 85% phosphatidylcholine.
5 . The composition of claim 1 wherein the phosphatidylcholine is soybean lecithin.
6 . The composition of claim 1 , wherein the phosphatidylcholine contains polyenylphosphatidylcholine.
7 . The composition of claim 1 , further comprising one or more of ascorbyl palmitate and lipoic acid.
8 . A method for treating skin comprising formulating a composition containing a phosphatidylcholine carrier and applying the composition to the skin.
9 . A method according to claim 8 , wherein the composition contains about 85% phosphatidylcholine.
10 . A method according to claims 8 , wherein the phosphatidylcholine is soybean lecithin.
11 . A method according to claims 8 , wherein the phosphatidylcholine contains polyenylphosphatidylcholine.
12 . A method according to claim 8 wherein the macromolecular drug is a polypeptide.
13 . A method according to claim 12 wherein the polypeptide is selected from the group consisting of oxytocin, vasopressin, insulin, somatotropin, calcitonin, chorionic gonadotropin, menotropins, follitropins, somatostatins, progestins, and combinations of any of these.
14 . A method according to claim 12 wherein the polypeptide is somatotropin.
15 . A method according to claim 12 wherein the polypeptide is insulin.
16 . A method for administering insulin to a patient comprising topically applying a composition comprising a crystal or non-polar phosphatidylcholine carrier and insulin to skin of the patient.
17 . The method of claim 16 , wherein the phosphatidylcholine carrier comprises about 85% phosphatidylcholine.
18 . A method according to claims 17 wherein the phosphatidylcholine carrier contains polyenylphosphatidylcholine.
19 . A composition for treating skin comprising phosphatidylcholine and at least one additional active ingredient.
20 . The composition of claim 1 , wherein the phosphatidylcholine is a polyenylphosphatidylcholine.Join the waitlist — get patent alerts
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