Method for extracting taxillus chinensis glycosides from rosa chinensis flowers
A technology of wide parasitic glycoside and Chinese rose, which is applied in the field of plant extraction and separation, can solve the problems of no extraction and separation of wide parasitic glycoside, and achieve the effects of beneficial multiple utilization, stable chemical properties, and easy elution and regeneration
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Embodiment 1
[0026] A method for extracting broadparasitin from Chinese rose, comprising the steps of:
[0027] 1) Take 2kg of dried rose flowers, crush them, and degrease them with petroleum ether for 3 times at room temperature. Extraction 3 times, each cold soaking extraction time is 7 days, 3 days, 3 days respectively, the extracts are combined and concentrated to obtain 600 g of total ethanol extract; among them, the addition ratio of dried rose flower and petroleum ether is 1 kg: 5L, the addition ratio of residue and ethanol is 1kg:5L;
[0028] 2) Dissolve the total ethanol extract (600 g) with an appropriate amount of methanol and mix the sample with a D101 macroporous resin column (600 g), and perform elution with water, 20% ethanol, and 40% ethanol in sequence through D101 macroporous resin column chromatography , evaporate the solvent to obtain 40% ethanol elution fraction;
[0029] 3) The fraction eluted with 40% ethanol was eluted by atmospheric silica gel column chromatograp...
Embodiment 2
[0036] A method for extracting broadparasitin from Chinese rose, comprising the steps of:
[0037] 1) Take 2kg of dried rose flowers, crush them, and degrease them with petroleum ether for 4 times at room temperature. Extracted 2 times, each cold soaking extraction time was 8 days and 3 days respectively, the extracts were combined and concentrated to obtain 510 g of total ethanol extract; among them, the addition ratio of dried rose flower and petroleum ether was 1 kg: 6 L, and the residue The addition ratio with ethanol is 1 kg: 6 L;
[0038] 2) Dissolve the total ethanol extract (510 g) with an appropriate amount of methanol and mix the sample with a D101 macroporous resin column (510 g). After chromatography on a D101 macroporous resin column, wash with water, 20% ethanol, and 40% ethanol in sequence. Remove and evaporate the solvent to obtain 40% ethanol elution fraction;
[0039]3) The fraction eluted with 40% ethanol was eluted by atmospheric silica gel column chromat...
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