US2012164241A1PendingUtilityA1
Boehmeria extract and its use in treating liver diseases
Est. expiryDec 27, 2030(~4.5 yrs left)· nominal 20-yr term from priority
A61P 35/00A61P 31/12A61P 1/16A61K 2236/331A61K 36/185
38
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Claims
Abstract
A pharmaceutical composition prepared from a Boehmeria species. This composition can be used to improve liver function and treat liver disease, and promoting liver tissue regeneration.
Claims
exact text as granted — not AI-modified1 . A pharmaceutical composition prepared by an extracting process comprising:
immersing a part of a Boehmeria species in water, removing the part of the Boehmeria species to obtain a solution, and concentrating the solution to provide a pharmaceutical composition, wherein the Boehmeria species is the only herb subjected to the extracting process.
2 . The pharmaceutical composition of claim 1 , wherein the Boehmeria species is Boehmeria nivea or Boehmeria frustescens thunberg.
3 . The pharmaceutical composition of claim 1 , wherein the immersing step is performed at a temperature between 20° C.-70° C.
4 . The pharmaceutical composition of claim 3 , wherein the immersing step is performed at a temperature between 25° C.-40° C.
5 . The pharmaceutical composition of claim 1 , wherein the immersing step is performed for 2-24 hours.
6 . The pharmaceutical composition of claim 2 , wherein the immersing step is performed at a temperature between 20° C.-70° C.
7 . The pharmaceutical composition of claim 6 , wherein the immersing step is performed at a temperature between 25° C.-40° C.
8 . The pharmaceutical composition of claim 7 , wherein the immersing step is performed for 2-24 hours.
9 . The pharmaceutical composition of claim 1 , wherein the extracting process further comprises enriching active components in the concentrated solution by chromatography.
10 . The pharmaceutical composition of claim 9 , wherein the chromatography is column chromatography or high performance liquid chromatography.
11 . The pharmaceutical composition of claim 10 , wherein the eluent used in the chromatography includes H 2 O, CH 3 CN, CH 3 OH, or a mixture thereof.
12 . The pharmaceutical composition of claim 8 , wherein the extracting process further comprises enriching active components in the concentrated solution by chromatography.
13 . The pharmaceutical composition of claim 12 , wherein the chromatography is column chromatography or high performance liquid chromatography.
14 . The pharmaceutical composition of claim 13 , wherein the eluent used in the chromatography includes H 2 O, CH 3 CN, CH 3 OH, or a mixture thereof.
15 . A method of improving liver function, comprising administering to a subject in need thereof an effective amount of a pharmaceutically composition of claim 1 .
16 . A method of improving liver function, comprising administering to a subject in need thereof an effective amount of a pharmaceutically composition of claim 14 .
17 . A method of treating liver disease, comprising administering to a subject in need thereof an effective amount of a pharmaceutically composition of claim 1 .
18 . The method of claim 17 , wherein the liver disease is liver fibrosis, liver cirrhosis, liver inflammation, hepatitis B virus infection, hepatitis C virus infection, or liver cancer.
19 . A method of treating liver disease, comprising administering to a subject in need thereof an effective amount of a pharmaceutically composition of claim 14 .
20 . The method of claim 19 , wherein the liver disease is liver fibrosis, liver cirrhosis, liver inflammation, hepatitis B virus infection, hepatitis C virus infection, or liver cancer.Cited by (0)
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