US2024033241A1PendingUtilityA1
Composition for external use on skin for inflammatory diseases
Est. expiryMay 12, 2031(~4.8 yrs left)· nominal 20-yr term from priority
A61K 9/0014A61K 31/202A61K 47/06A61K 31/683A61P 17/00A61P 17/04A61K 31/232A61K 31/685A61K 31/7032A61P 17/02A61P 17/06A61P 19/02A61P 29/00A61P 37/08
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Claims
Abstract
[Problem] To provide a composition for external skin use that has anti-inflammatory and antiallergic activity and is very safe. [Solution] A composition for external skin use for inflammatory diseases contains dihomo-gamma-linolenic acid (DGLA) as the active ingredient thereof. It is preferable for the DGLA to be present as a glyceride, a phospholipid, or an alkyl ester. The amount of DGLA contained in the composition for external use is 0.1-50 wt %.
Claims
exact text as granted — not AI-modified1 . A method for treating inflammatory disease comprising administering topically, to the skin of a patient in need thereof, an effective amount of dihomo-γ-linolenic acid (DGLA).
2 . The method according to claim 1 , wherein the dihomo-y-linolenic acid (DGLA) is in the form of any one of a glyceride, a phospholipid, a glycolipid, an alkyl ester, a salt, or a free fatty acid.
3 . The method according to claim 2 , wherein the glyceride is a triglyceride, a diglyceride, or a monoglyceride.
4 . The method according to claim 2 , wherein the alkyl ester is an ester with a lower C 1-4 alcohol.
5 . The method according to claim 2 , wherein the phospholipid is diacylglycerophospholipid or lysoacylglycerophospholipid.
6 . The method according to claim 1 , wherein the dihomo-γ-linolenic acid (DGLA) is administered in a composition containing 0.01 to 50 wt % of the dihomo-γ-linolenic acid (DGLA).
7 . The method according to claim 1 , wherein the inflammatory disease is an inflammatory skin disease.
8 . The method according to claim 7 , wherein the inflammatory disease is atopic dermatitis, allergic contact dermatitis, irritant contact dermatitis, psoriasis, rheumatism, or lupus.
9 . The method according to claim 1 , wherein the dihomo-γ-linolenic acid (DGLA) is administered in a composition containing 0.01 to 50 wt % of the dihomo-γ-linolenic acid (DGLA) and wherein the composition is applied continuously for at least 7 consecutive days to an area affected by the inflammatory disease.
10 . The method according to claim 9 , wherein the dihomo-γ-linolenic acid (DGLA) is administered in a composition containing 0.05 to 10 wt % of the dihomo-γ-linolenic acid (DGLA) and wherein the composition is applied continuously for at least 7 consecutive days to an area affected by the inflammatory disease.
11 . The method according to claim 10 , wherein the dihomo-γ-linolenic acid (DGLA) is administered in a composition containing 0.05 to 7 wt % of the dihomo-γ-linolenic acid (DGLA) and wherein the composition is applied continuously for at least 7 consecutive days to an area affected by the inflammatory disease.
12 . The method according to claim 9 , wherein the dihomo-γ-linolenic acid (DGLA) is administered in a composition containing 0.01 to 50 wt % of the dihomo-γ-linolenic acid (DGLA) and wherein the composition is applied continuously for at least 10 consecutive days to an area affected by the inflammatory disease.
13 . The method according to claim 9 , wherein the dihomo-γ-linolenic acid (DGLA) is administered in a composition containing 0.01 to 50 wt % of the dihomo-γ-linolenic acid (DGLA) and wherein the composition is applied continuously for at least 14 consecutive days to an area affected by the inflammatory disease.
14 . The method according to claim 1 , which is for suppressing the itch of the inflammatory disease.Join the waitlist — get patent alerts
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