Method for preparing schaftoside from desmodium styracifolium
A technology of schaftoside and Desmodium sativa, applied in the field of natural medicinal chemistry, can solve the problems of poor reproducibility of silica gel column chromatography, unsuitability for the preparation of schiaftoside, complicated operation, etc., shorten the extraction cycle and increase the amount of preparation Great, easy-to-operate effects
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Embodiment 1
[0018] Dissolve 10g of cellulase in 5L of water, add 5kg of crushed Desmodium sativa, mix well, enzymatically hydrolyze at room temperature for 5 days, soak and extract the raw material for enzymolysis with warm water at 70°C for 2 times, add 40kg each time, filter the extract with molecular weight cut-off 2000 hollow cellulose ultrafiltration membrane for ultrafiltration, and the permeate was concentrated with a hollow cellulose nanofiltration membrane with a molecular weight cut off of 200. The obtained concentrated solution was extracted 3 times with an equal volume of ethyl acetate, and the extract was concentrated to obtain 20 g of crude extract. Mix ethyl acetate, n-butanol, and water in a ratio of 3:1:4. After fully layering, take the upper phase and fill the high-speed countercurrent chromatography column. At the same time, turn on the main engine at 900 rpm, pump the lower phase into the mobile phase, and wait for the system to balance Finally, the flow rate is adjuste...
Embodiment 2
[0020] Dissolve 10g of amylase 5 and pectinase in 5L of water, add 5kg of crushed Desmodium sativa, mix well, enzymatically hydrolyze at room temperature for 4 days, soak and extract the raw materials for enzymolysis with warm water at 60°C for 3 times, add 30kg each time, and extract After filtration, use a hollow cellulose ultrafiltration membrane with a molecular weight cut-off of 6000 for ultrafiltration, and then concentrate the permeate with a hollow cellulose nanofiltration membrane with a molecular weight cut-off of 300. The obtained concentrated solution is extracted 3 times with an equal volume of ethyl acetate, and the extract is concentrated to obtain Crude extract 12g. Mix ethyl acetate, n-butanol, and water in a ratio of 3:2:5. After fully layering, take the upper phase and fill the high-speed countercurrent chromatography column. At the same time, turn on the main engine at 800 rpm, pump the lower phase into the mobile phase, and wait for the system to balance F...
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