Method for extracting tetrandrine and fangchinoline from radix stephaniae tetrandrae
A technology of antipredyl and antipredyl, applied in the direction of organic chemistry, etc., can solve the problems of low extraction rate of antiprednisone and the generation of a large amount of waste water, so as to save medicinal resources of antiprednis, increase production rate, reduce The effect of production costs
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Embodiment 1
[0022] Take 100kg of dried Fangzi root and crush it, add water until the water content reaches 35%, add 10L of Bacillus subtilis to ferment for 2 days, then add 12L of yeast to ferment for 3 days, add 200L of 75% ethanol solution to reflux for extraction for 2 hours, filter, and pour into the filter residue Add 200L of 75% ethanol solution to reflux to extract for 2h, filter, combine the two filtrates, and concentrate the filtrate under reduced pressure at 55°C to 20L to obtain a concentrated solution; add 0.1mol / L hydrochloric acid to the concentrated solution to pH2.5, and use 60L butanol Extract to obtain aqueous phase A and butanol extract A; add 0.001mol / L sodium hydroxide solution to butanol extract A to pH 9, stand and separate to obtain 5L solution C (without butanol), use 0.1mol / L L hydrochloric acid to pH 2.5, extracted with 20L butanol to obtain butanol extract B; butanol extract B was concentrated to dryness under reduced pressure at 55°C to obtain 2.48kg of dry pro...
Embodiment 2
[0028] Take 200kg of dried Fangzi roots and crush them, add water until the water content reaches 40%, add 20L of Bacillus subtilis to ferment for 2 days, then add 22L of yeast to ferment for 3 days, add 500L of 75% ethanol solution to reflux for extraction for 2 hours, filter, and pour into the filter residue Add 300L of 75% ethanol solution to reflux to extract for 2h, filter, combine the two filtrates, and concentrate the filtrate under reduced pressure at 55°C to 40L to obtain a concentrated solution; add 0.1mol / L hydrochloric acid to the concentrated solution to pH2.5, and use 120L butanol Extract to obtain aqueous phase A and butanol extract A; add 0.001mol / L sodium hydroxide solution to butanol extract A to pH9, leave to stand and separate to obtain 8L solution C (without butanol), use 0.1mol / L L hydrochloric acid to pH 2.5, extracted with 30L butanol to obtain butanol extract B; butanol extract B was concentrated to dryness under reduced pressure at 50-65°C to obtain 5....
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