Method for preparing valid target in gavel fruit vine fruit and application of the same
A technology of effective parts and mallet vine, applied to medical preparations containing active ingredients, pharmaceutical formulas, capsule delivery, etc., can solve the problems of extraction of medicinal parts, pharmacology and mechanism of action research reports, etc., and achieve curative effect Significant, reasonable method design, low cost effect
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Embodiment 1
[0017] Embodiment 1 The preparation of the effective part of the mallet fruit vine
[0018] Take about 200g of the vine fruit and crush it, add 1600ml of ethanol, reflux for extraction for 2 hours, filter the filter residue and add 1000ml of ethanol to reflux for 1 hour, combine the two filtrates, recover the ethanol under reduced pressure, and obtain the extract. Suspend this extract with 200ml of water, extract it with petroleum ether three times to degrease, then extract it with n-butanol three times until the extraction layer is nearly colorless, combine the n-butanol extracts, concentrate to obtain 3.08g of medicinal parts .
Embodiment 2
[0019] Embodiment 2 The preparation of the effective part of the mallet fruit vine
[0020] Take about 200g of vine fruit and crush them, add 50% ethanol to percolate and extract for a week, after the percolates are combined, the ethanol is recovered completely under reduced pressure, and the remaining water phase is extracted three times with n-hexane to degrease, and then coated with AB-8 macroporous resin to After elution with water for 3 column volumes, elute with 70% ethanol until the effluent is nearly colorless, collect this part of the eluate, concentrate under reduced pressure to recover ethanol and then spray dry to obtain 2.92 g of medicinal parts.
Embodiment 3
[0021] Embodiment 3 Preparation of the effective part of Hammer fruit vine
[0022] Take about 200g of vine fruit and crush it, add 1600ml of methanol, reflux for extraction for 2 hours, filter the filter residue and add 1000ml of methanol to reflux for 1 hour, combine the two filtrates, recover the methanol under reduced pressure, and obtain the extract. Suspend the extract with 200ml of water, extract it with cyclohexane three times to degrease, then extract it with n-butanol three times until the extraction layer is nearly colorless, combine the n-butanol extracts, concentrate to obtain 3.06g of medicinal extract parts.
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