Method for extracting golden buckwheat high polymeric proanthocyanidin and preparing oligomeric proanthocyanidin by carrying out catalytic degradation on same
A technology for high-polymer procyanidins and an extraction method, which is applied in the field of extraction and catalytic degradation of golden buckwheat high-polymer procyanidins to prepare oligomeric procyanidins, can solve problems such as the degradation method of golden buckwheat high-polymer procyanidins and the like, and achieves a high yield. Effect
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Embodiment 1
[0021] (1) Grinding the traditional Chinese medicine golden buckwheat, the particle size of which is about 1-3 cm, to obtain the crude product of golden buckwheat;
[0022] (2) Extract 200 g of the above-mentioned golden buckwheat crude product with 50% ethanol solution, the ratio of material to solution is 1:6, the temperature is 50°C, and the time is 24 hours;
[0023] (3) Ethanol was evaporated from the extract, water was added to 600ml, centrifuged for 10min after stirring, the rotation speed was 3000rpm, the precipitate was discarded, the supernatant was extracted twice with equal volume of ethyl acetate, and the aqueous phase raffinate was collected;
[0024] (4) Put the aqueous phase raffinate on the LSA-21 macroporous resin column, first wash with 3 column volumes of distilled water, and then elute with 3 column volumes of 50% ethanol solution. The collected eluate was concentrated under reduced pressure and dried to obtain 10.23 g of high-polymeric proanthocyanidins f...
Embodiment 2
[0026] (1) Grinding the traditional Chinese medicine golden buckwheat, the particle size of which is about 1-3 cm, to obtain the crude product of golden buckwheat;
[0027] (2) Extract 300 g of the above-mentioned golden buckwheat crude product with 60% ethanol solution, the ratio of material to solution is 1:10, the temperature is 50° C., and the time is 24 hours;
[0028] (3) Remove ethanol from the extract, add water to 1500ml, centrifuge for 10min after stirring, at a speed of 5000rpm, discard the precipitate, extract the supernatant twice with equal volume of ethyl acetate, and collect the aqueous phase raffinate;
[0029] (4) Put the aqueous phase raffinate on the LSA-21 macroporous resin column, wash with 2 times column volume of distilled water, and then elute with 4 column volumes of 70% ethanol solution. The collected eluate was concentrated under reduced pressure and dried to obtain 12.11 g of high-polymeric proanthocyanidins from golden buckwheat, with a proanthocy...
Embodiment 3
[0031] (1) Grinding the traditional Chinese medicine golden buckwheat, the particle size of which is about 1-3 cm, to obtain the crude product of golden buckwheat;
[0032] (2) Extract 400 g of the above-mentioned golden buckwheat crude product with 50% ethanol solution, the ratio of material to solution is 1:8, the temperature is 50° C., and the time is 24 hours;
[0033] (3) Ethanol was evaporated from the extract, water was added to 1600ml, centrifuged for 10min after stirring, the rotating speed was 5000rpm, the precipitate was discarded, the supernatant was extracted twice with equal volume of ethyl acetate, and the aqueous phase raffinate was collected;
[0034] (4) Put the aqueous phase raffinate on the LSA-21 macroporous resin column, first wash with 2 times column volume of distilled water, and then elute with 5 column volumes of 50% ethanol solution. The collected eluate was concentrated under reduced pressure and dried to obtain 22.24 g of high-polymeric proanthocya...
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