Method and system for extracting and separating flavone glycoside monomer from Desmodium styracifolium
A technology of Radix vulgaris and its extract is applied in the field of phytochemistry and achieves the effects of short production time, high product yield and simple process operation.
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Embodiment 1
[0031] Figure 4 A general scheme of the method of the invention is shown.
[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. After the adsorption...
Embodiment 2
[0047] 1. Carry out steps 1-3 of Example 1.
[0048] 2. Multi-stage chromatographic separation
[0049] (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;
[0050] (2) Use ODS reversed-phase medium-pressure chromatography to separate 65% of the part obtained by chromatographic separation I, that is, chromatographic separation II, use ethanol-water, the condition is 20% isocratic for 30 minutes, and 20-40% gradient is eluted for 200 minutes, according to the chromatographic Figure out the peak sequence, collect in fractions, collect one fraction per 100-150 volume fractions, collect 40-50 fractions in total, and merge the same fractions after HPLC detection;
[0051] (3) Combine the 36-50 fract...
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