US2015094292A1PendingUtilityA1
Topical compositions containing nitro fatty acids
Est. expiryDec 31, 2028(~2.4 yrs left)· nominal 20-yr term from priority
Inventors:Raymond A. Miller
A61P 17/06A61P 17/10A61P 17/00A61Q 19/00A23L 33/15A61K 31/355A61K 31/201A23L 33/12A61K 8/40A61K 8/361A61K 31/575A61K 9/0014A61K 8/11A61K 31/20A23L 33/10A23P 10/30A61K 2800/92Y02A50/30
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Claims
Abstract
Activated fatty acids, topical compositions including activated fatty acids and methods for using activated fatty acids to treat a variety of diseases.
Claims
exact text as granted — not AI-modified1 . A topical composition comprising:
at least one activated fatty acid; and dermatologically acceptable vehicle.
2 . A method comprising applying the topical composition of claim 1 to the skin of a patient in need of treatment.
3 . The method of claim 2 , further comprising treating inflammation in the skin of a patient in need of treatment.
4 . A composition for the prevention of skin damage comprising: an effective amount of a nitroalkene in a dermatologically acceptable non-polar carrier.
5 . A method for the prevention and treatment of skin damage comprising: topically applying a composition containing an effective amount of a nitroalkene in a dermatologically acceptable non-polar carrier to damaged skin tissue.
6 . The method of claim 5 , wherein the nitroalkene is nitro-linoleic acid, nitro-oleic acid, nitrated arachidonic acid, or nitrated cholesteryl lineolate.
7 . The method of claim 5 , wherein the nitroalkene is present in a weight percentage which is within one of the following ranges:
0.01%-0.025%; 0.025%-0.05%; 0.05%-0.10%; 0.10%-0.50%; 0.50%-1.0%; 0.025%-0.50%; 0.025%-1.0%; 1.0%-2.0%; 2.0%-5.0%; 5.0%-10.00% 1.0%-5.0%; 1.0%40.0%; 10.0%-20.0%; 20.0%-30.0%; 30.0%-40.0%; 40.0%-50.0%; 50.0%-60.0%; 60.0%-70.0%; 70.0%-80.0%; 80.0%-90.0%; 90.0%-98.0%; 10.0%-30.0%; 20.0%-40.0%; 30.0%-60.0%; 40.0%-70.0%; 50.0%-80.0%; 10.0%-50.0%; 10.0%-98.0%; 50.0%-70.0%; 50.0%-98.0%; or 70.0%-98.0%.
8 . The method of claim 5 , wherein the non-polar carrier comprises one or more of: polyethylene glycols, glycerides, glycerin; polypropylene glycol; PVM/MA decadiene crosspolymer; hydrogenated polyisobutane/polyethane; isododecane; tetrahexyldecyl ascorbate; Vitamin E; beta carotene; disopropyl adipate; 2-ethylhexyl pentate; oleth-3; propanoic acid 2-hydroxy-dodecyl ester; propanoic acid, 2-hydroxy-, C12-15-alkyl esters; glycereth-4; glycereth-7; diglycerin; panthenol; and phytantriaol.
9 . The method of claim 8 , wherein the non-polar carrier comprises one or more polyethylene glycols.
10 . The method of claim 8 , wherein the skin inflammation is one or more of: acne, aging skin, alopecia, dermatitis, xerosis, eczema, rosacea, seborrhea, and psoriasis.
11 . The method of claim 5 , wherein the non-polar carrier comprises a polymer polyether.
12 . The method of claim 5 , wherein the carrier further comprises a phosphatidylcholine.
13 . The method of claim 5 , wherein said composition further comprises one or more additional ingredients selected from the group consisting of: fatty acid esters of ascorbic acid, lipoic acid, and tocotrienols and tocotrienol derivatives and vitamin E compositions enriched with tocotrienol or tocotrienol derivatives.
14 . The method of claim 5 , wherein the skin damage is one or more of: cut, abrasion, burn, blemish, cutaneous scar tissue, lesion, acne, aging skin, alopecia, dermatitis, xerosis, eczema, rosacea, seborrhea, and psoriasis; or skin inflammation.Join the waitlist — get patent alerts
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