Method for extracting, separating and purifying Astragaloside IV from Astragalus mongholicus
A technology for astragaloside IV and astragalus, which is applied in the field of extracting, separating and purifying astragaloside IV from astragalus, can solve the problems of low content, difficulty in separation and purification, etc., and achieve the effects of high purity, high yield, and simple and easy method.
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Embodiment 1
[0032] Accurately weigh 1000 g of traditional Chinese medicine Astragalus membranaceus, dissolve 0.2% solid weight of mixed enzymes (cellulase, pectinase, β-glucosidase) in 10 times the volume of warm water, and continuously homogenize and extract 3 times, each time for 1 min. Put the homogenate in a constant temperature shaker at 30°C for constant temperature enzymolysis for 12 hours, after suction filtration of the enzyme-inducing solution, add 70% ethanol to the filter residue for negative pressure cavitation extraction, the pressure is 0.05Mpa, and the solid-liquid ratio is 1:10 (g:mL ), extracted at room temperature 3 times, each time for 45min, the enzymatic hydrolyzate and the extract after suction filtration were combined, concentrated under reduced pressure to dryness, then dissolved in water, adjusted to pH 8 with ammonia water, hydrolyzed for 12h, and the hydrolyzed solution obtained was An equal volume of n-butanol was used as a solvent, extracted three times, and c...
Embodiment 2
[0034] Accurately weigh 1000 g of the traditional Chinese medicine Astragalus membranaceus, dissolve 0.5% solid weight of mixed enzymes (cellulase, pectinase, β-glucosidase) in 15 times the volume of warm water, and continuously homogenize and extract 3 times, each time for 2 minutes. Put the homogenate in a constant temperature shaker at 30°C for constant temperature enzymolysis for 24 hours. After the enzyme-inducing solution is suction-filtered, the filter residue is extracted by negative pressure cavitation with 80% ethanol. The pressure is 0.06Mpa, and the solid-liquid ratio is 1:15 (g:mL ), extraction at room temperature 3 times, 60min each time, the enzymolysis solution after suction filtration and the extraction solution were combined, concentrated under reduced pressure to dryness and then dissolved in water, adjusted to pH 9 with ammonia water, hydrolyzed for 24h, and the hydrolyzed solution obtained was An equal volume of n-butanol was used as a solvent, extracted 4 ...
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