A pueraria root scutellaria and coptis extract
A technology of pueraria chinensis and extracts, which is applied in the directions of drug combinations, plant raw materials, plant/algae/fungus/moss components, etc., can solve the problems of difficult quality control, inability to guarantee stable curative effect, low content of active ingredients, etc. Improvement, drug quality and stable efficacy
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example 1
[0064] Take 2.4Kg of Pueraria Radix, 0.9Kg of Radix Scutellariae, 0.9Kg of Coptis Rhizoma, and 0.6Kg of Glycyrrhizae, decoct twice with 6 times and 4 times of water, each time for 0.5 hours, filter, combine the filtrates, concentrate to 1 / 4 of the original volume, Add conc The amount is 65%, filter, and the filtrate is concentrated to 1.6Kg, puts on macroporous resin column (macroporous resin consumption is 6.2Kg), first with 4 times column volume deionized water elution, then with 40% ethanol of 3 times resin volume Elution, collect the ethanol eluate, recover the solvent under reduced pressure, mix the extract with the above precipitation, and dry to obtain about 238g of total extract, which contains 13.5% of total isoflavones of Pueraria radix, 20.5% of total flavonoids of Scutellaria baicalensis; total alkaloids of Coptis chinensis 10.5%, glycyrrhizic acid 2.0%.
example 2
[0066] Take 2.4Kg of Pueraria Radix, 0.9Kg of Radix Scutellariae, 0.9Kg of Coptis Rhizoma, and 0.6Kg of Glycyrrhizae, decoct twice with 10 times and 8 times of water, each time for 1 hour, filter, combine the filtrates, concentrate to 1 / 3 of the original volume, Add concentrated hydrochloric acid to adjust the pH to 1-2, and then separate the precipitate and supernatant after standing for 18 hours; take the precipitate and wash it to pH 5-6 for later use; take the supernatant to adjust the pH to 5-6, concentrate to a density of 1.15, add ethanol until the alcohol content is 70%, filter, and the filtrate is concentrated to 2.0Kg, put on a macroporous resin column (the amount of macroporous resin is 9.6Kg), first elute with 5 times of column volume deionized water, and then elute with 50% ethanol of 4 times of resin volume , collect the ethanol eluate, recover the solvent under reduced pressure, mix the extract with the above precipitation, and dry to obtain about 354g of the tot...
example 3
[0068] Take 2.4Kg of Pueraria Radix, 0.9Kg of Radix Scutellariae, 0.9Kg of Coptidis Rhizoma, and 0.6Kg of Glycyrrhizae, decoct twice with 12 times and 10 times of water for 1.5 hours each time, filter, combine the filtrates, concentrate to 1 / 3 of the original volume, Add concentrated hydrochloric acid to adjust the pH to 1-2, and then separate the precipitate and supernatant after standing for 24 hours; take the precipitate and wash it to pH 5-6 for later use; take the supernatant to adjust the pH to 5-6, concentrate to a density of 1.20, add ethanol until the alcohol content is 75%, filter, and the filtrate is concentrated to 2.4Kg, put on a macroporous resin column (the amount of macroporous resin is 14.4Kg), first elute with 6 times the column volume of deionized water, and then elute with 70% ethanol with 5 times the volume of the resin , collect the ethanol eluate, recover the solvent under reduced pressure, mix the extract with the above precipitation, and dry to obtain a...
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