Method for preparing hyperoside and isoquercetin from cotton petal
A technology of hyperoside and isoquercetin, which is applied in the direction of pharmaceutical formulas, medical preparations containing active ingredients, plant raw materials, etc.
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Embodiment 1
[0023] a. Using cotton petals as raw material, crush the dried cotton petals into coarse powder, add 8 times of 70% ethanol to heat and reflux to extract twice, each time for 2 hours, combine the extracts, and concentrate to obtain the extract;
[0024] b. Concentrate the extract to extract under reduced pressure, add water to dissolve, then put the aqueous solution on the AB-8 macroporous resin column, and wash the column bed with water until it is colorless;
[0025] c. Then wash 5 column volumes with 30% ethanol, collect the eluate, and concentrate to obtain crude products of hyperin and isoquercetin;
[0026] d. Dissolve the crude product in ethyl acetate, apply silica gel column chromatography, and elute with petroleum ether-ethyl acetate-methanol-acetic acid solution to obtain pure products of hyperin and isoquercetin.
Embodiment 2
[0028] a. Using cotton petals as raw material, crush the dried cotton petals into coarse powder, add 15 times of methanol, perform ultrasonic extraction for 3 times, each time for 1 hour, and combine the extracts;
[0029] b. Concentrate the extract to an extract under reduced pressure, add water to dissolve, then put the aqueous solution on a D101 macroporous resin column, and wash the column bed with water until it is colorless;
[0030] c. Then wash 4 column volumes with 50% ethanol solution, collect the eluate, and concentrate to obtain crude products of hyperin and isoquercetin;
[0031] d. After dissolving the crude product with aqueous methanol, apply C18 silica gel column chromatography and elute with 90% aqueous methanol to obtain pure hyperin and isoquercetin.
Embodiment 3
[0033] a. Using cotton petals as raw material, crush the dried cotton petals into coarse powder, add 20 times of acetone, heat and microwave-assisted extraction for 3 times, each time for 30 minutes, and combine the extracts;
[0034] b. Then concentrate the extract under reduced pressure to extract, add water to dissolve, then put the aqueous solution on the NKA-9 macroporous resin column, and wash the column bed with water until it is colorless;
[0035] c. Then wash 3 column volumes with 40% ethanol, collect the eluate, concentrate, and obtain crude products of hyperin and isoquercetin;
[0036] d. Dissolve the crude product in ethyl acetate, apply C18 silica gel column chromatography, and elute with 80% aqueous methanol to obtain pure hyperin and isoquercetin.
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