Method and system for extracting and separating dihydro-phaseic acid from desmodium styracifolium
A technology for separating dihydro safflower and quinceum chinensis, which is applied in the field of phytochemistry and achieves the effects of short production time, simple process operation and high purity
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Embodiment 1
[0031] Figure 5 Show the general flow process of the inventive method, comprise following:
[0032] 1. Raw materials: select 45000-50000 parts by weight of the leguminous plant Desmodium glabrata, cut into 5-10cm sections, wash off the sediment with drinking water, drain and feed.
[0033] 2. Ethanol extraction: reflux extraction with 80% ethanol twice, the first time 12 times the amount for 2 hours, the second time 10 times the amount for 1.5 hours; combine the two alcohol extracts, and recover the ethanol until it has no alcohol smell.
[0034] 3. Concentration under reduced pressure: add water to dilute the extract concentrate to 5 times the volume of the medicinal material; filter it with a 200-mesh filter cloth; get the column liquid; pack the net product resin that has been treated with 95% ethanol in advance, and replace it with purified water; The upper column liquid is pumped into the column for adsorption, and the flow rate is controlled to be 0.5-1 times BV / h. Aft...
Embodiment 2
[0045] 1. Carry out steps 1-3 of Example 1 to obtain Guangjin bulk drug.
[0046] 2. Tertiary chromatographic separation
[0047] (1) 300-400 parts by weight of Guangjin crude drug is separated by AB-8 macroporous resin chromatography, that is, chromatographic separation I, ethanol-water mixed solvent 25:75, 35:65, 45:55, 65:35 gradient washing Take off, wash each gradient until there is no color, combine the fractions to get 25%, 35%, 45%, and 65% in four parts.
[0048] (2) The 25% part obtained by chromatography I is separated by ODS reverse-phase medium-pressure chromatography, that is, chromatographic separation II, using ethanol-water, the condition is 15% isocratic for 300 minutes, and 15-35% gradient is eluted for 200 minutes, according to the chromatogram. Peak sequence, collected in fractions, one portion per 100-150 volume fractions, a total of 40-50 fractions were collected, and the same fractions were combined after HPLC detection; 30-40 fractions obtained from c...
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