Longbract cattail general flavone extractive and its prepn and use
A technology of extracts and total flavonoids, applied in the field of medicine, can solve problems such as the undiscovered total flavonoids extract from Puhuang
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Embodiment 1
[0045] Put 1kg of raw Pollen in a 10L round bottom flask, add 7kg of 70% ethanol, stir well, heat and reflux in a water bath for extraction for 2 hours, filter while hot, and then heat and extract the residue with 5kg of 70% ethanol for 1 hour , filtered while hot, and combined the filtrates. The filtrate is reclaimed under reduced pressure with a rotary evaporator to a thick extract with a specific gravity of 1.1 to 1.2, and 10% ethanol solution is added in a ratio of 1:10, and a chitosan clarifying agent is added in a ratio of 1% of the total volume simultaneously, and the Centrifuge and filter after reaching room temperature. The filtrate is adsorbed on the pre-treated 1kg HZ-802 macroporous adsorption resin (produced by Shanghai Huazhen Technology Trading Co., Ltd.) column bed. After all the filtrate passes through, the column bed is first washed with 8 to 10 liters of deionized water until clarified. , and then use 10 to 12 liters of 30% ethanol to rinse until the color ...
Embodiment 2
[0046] Put 1kg of raw Pollen in a 10L round bottom flask, add 7kg of 70% ethanol, stir well, heat and reflux in a water bath for extraction for 2 hours, filter while hot, and then heat and extract the residue with 5kg of 70% ethanol for 1 hour , filtered while hot, and combined the filtrates. The filtrate was recovered to 3 L (the specific gravity was about 1.05) with a rotary evaporator under reduced pressure, and 500 ml of saturated lead acetate aqueous solution was added, fully stirred, and allowed to stand for precipitation. The precipitate was collected by centrifugation. Suspend the precipitate in 2.5L of 95% ethanol, pass through H2S for metathesis, centrifuge to remove the lead sulfide precipitate, recover ethanol from the filtrate, vacuum-dry and pulverize to obtain 143 g of total flavonoids extract of Puhuang. After determination, the total flavonoid content is 54.2%. Embodiment 3: the preparation technology of high-purity total flavonoids of Puhuang
Embodiment 3
[0047] Get 5g of the total flavonoids extract of Puhuang obtained in the above-mentioned embodiment 1 or embodiment 2, dissolve in an appropriate amount of methanol, 500g Sephadex-LH20 column chromatography on the solution, elute with methanol, collect the main color bands respectively, reclaim the solvent to After drying, 1.25 g of isorhamnetin-3-O-(2G-α-L-rhamnosyl)-rutinoside and 0.98 g of isorhamnetin-3-O-neohesperidoside were obtained respectively. After determination, the content of the former component is 96.4%; the content of the latter component is 98.5%. Embodiment 4: the preparation technology of sodium salt derivative
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