Sargentodoxae caulis proantho cyanidins and preparation method thereof
A technology of proanthocyanidins and anthocyanidins, applied in the direction of organic chemistry, etc., can solve the problems such as the preparation method of anthocyanidins from the vines that have never been seen before, and achieve the effect of great practical significance and promotion value.
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Embodiment 1
[0031] Preparation, ultraviolet and infrared spectroscopic analysis and content determination of a kind of proanthocyanidin
[0032] Weigh 50g of dry Rhizoma sagittata coarse powder, add 500mL of 70% acetone, in an ultrasonic generator, ultrasonically extract at 40KHz for 30min, filter with Buchner funnel, extract 3 times in total, combine the filtrates for 3 times, and put the filtrate in rotary evaporation Concentrate under reduced pressure at 38°C in a container to obtain the concentrated solution of Sargentina radix, put the concentrated solution in a separatory funnel, extract 3 times with petroleum ether, collect the water layer, and obtain the degreased sageteng concentrated solution, the concentrated solution is diluted with 0.45 μm microporous membrane filtration, used for Sephadex LH-20 purification.
[0033] Take 100g of Sephadex LH-20 filler, fully swell with 50% volume fraction of methanol, wet-pack the column, and then equilibrate the column with 1200mL 50% volum...
Embodiment 2
[0055] Preparation of a kind of Rhododendron proanthocyanidin
[0056] Weigh 100g of dry S. sanctana coarse powder, add 1000mL of 65% ethanol, reflux extraction at 60°C for 3 times, extract for 1 hour each time, filter, and concentrate the filtrate in a rotary evaporator at 50°C under reduced pressure to obtain S. Concentrated solution, put the concentrated solution in a separatory funnel, extract 3 times with petroleum ether, collect the water layer, and obtain the degreased Rhizoma sagittarius concentrated solution, filter the concentrated solution with a 0.45 μm microporous membrane filter, and use it for Sephadex LH- 20 purification.
[0057] Take 100g of Sephadex LH-20 filler, fully swell with 50% volume fraction of methanol, wet-pack the column, and then equilibrate the column with 1200mL 50% volume fraction of methanol. , eluted with 50% volume fraction of methanol to fully remove polysaccharides, peptides, saponins, terpenes, flavonoids and small molecule phenols unti...
Embodiment 3
[0061] Preparation of a kind of Rhododendron proanthocyanidin
[0062] Weigh 100g of dry Rhizoma sagittata coarse powder, add 1000mL of 70% acetone, stand and extract for 3 times, extract for 24 hours each time, filter, and concentrate the filtrate under reduced pressure in a rotary evaporator at 40°C to obtain the concentrate of Rhizoma sagittata , put the concentrated solution in a separatory funnel, extract 3 times with petroleum ether, collect the water layer, and obtain the degreased Rhizoma sagittata concentrated solution, which is filtered through a 0.45 μm microporous membrane and used for Sephadex LH-20 purification .
[0063] Take 100g of Sephadex LH-20 filler, fully swell with 50% volume fraction of methanol, wet-pack the column, and then equilibrate the column with 1200mL 50% volume fraction of methanol. , eluted with 50% volume fraction of methanol to fully remove polysaccharides, peptides, saponins, terpenes, flavonoids and small molecule phenols until the eluen...
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