US2018214503A1PendingUtilityA1
Composition for wound treatment containing extract of stellera chamaejasme or fraction thereof and method for treating wound of subject
Est. expiryApr 13, 2035(~8.8 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 17/02A61P 17/00A61K 9/4858A61K 9/2018A61K 36/83A61K 8/96A61K 9/2009A61K 9/2059A61K 8/9789A61K 9/1652A61K 8/97A61K 2236/00A61Q 19/08A61K 9/1623A61K 9/4875
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Claims
Abstract
Provided are a composition including Stellera chamaejasme extract for treating wound, a method of treating wound of a subject, a cosmetic composition for wound improving, skin wrinkle improving, or skin anti-aging, and a method of cosmeticizing for wound improving, skin wrinkle improving, or skin anti-aging.
Claims
exact text as granted — not AI-modified1 . A pharmaceutical composition for treating a wound, comprising a Stellera chamaejasme extract or a fraction thereof as an active ingredient, wherein the Stellera chamaejasme extract is extracted from an aerial part of Stellera chamaejasme.
2 . The pharmaceutical composition of claim 1 , wherein the Stellera chamaejasme extract is extracted in water, acetone, a C 1 -C 6 alcohol, or a combination thereof.
3 . The pharmaceutical composition of claim 1 , wherein the Stellera chamaejasme extract is extracted in 75% (v/v) to 100% (v/v) ethanol, 75% (v/v) to 100% (v/v) methanol, 75% (v/v) to 100% (v/v) butanol, or a combination thereof.
4 . The pharmaceutical composition of claim 1 , wherein the fraction is a hexane fraction; an ethyl acetate fraction; a butanol fraction; or a combination thereof, wherein the hexane fraction, the ethyl acetate fraction, and the butanol fraction are obtained by suspending Stellera chamaejasme extract in water and then subsequently fractionating a suspension by using hexane, ethyl acetate, and butanol.
5 . The pharmaceutical composition of claim 1 , wherein the wound is a skin wound.
6 . The pharmaceutical composition of claim 1 , wherein an amount of the Stellera chamaejasme extract or the fraction thereof is in a range of 0.001 percent by weight (wt %) to 80 wt %, based on an amount of the pharmaceutical composition.
7 . The pharmaceutical composition of claim 1 , further comprising a pharmaceutically acceptable excipient or carrier.
8 . The pharmaceutical composition of claim 1 , wherein treatment of the wound is by promoting expression of a collagen gene in a cell.
9 . A method of treating a wound of a subject, comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 1 to the subject to treat the wound.
10 . A method of treating a wound of a subject, comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 2 to the subject to treat the wound.
11 . A method of treating a wound of a subject, comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 3 to the subject to treat the wound.
12 . A method of treating a wound of a subject, comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 4 to the subject to treat the wound.
13 . A method of treating a wound of a subject, comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 5 to the subject to treat the wound.
14 . A method of treating a wound of a subject, comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 6 to the subject to treat the wound.
15 . A method of treating a wound of a subject, comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 7 to the subject to treat the wound.
16 . A method of treating a wound of a subject, comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 8 to the subject to treat the wound.Cited by (0)
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