Application of total flavones of chickpea in preparation of medicament for treating diabetes
A technology of diabetes medicine and total flavonoids, which is applied in the application field of chickpea total flavonoids in the preparation of diabetes medicines, can solve the problems of low flavonoid content and no medicinal value, and achieve the effect of low cost and simple extraction process
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Embodiment 1
[0019] Step 1: Put 200g of chickpea powder crushed to 0.5-5mm in a round bottom flask, add 1000ml of petroleum ether, heat to a slight boil and reflux for 1h, filter and collect the chickpea powder, add 1000ml of petroleum ether and reflux for 1h, Repeat a total of three times. Dry the obtained defatted chickpea powder and add 2400ml of 80% ethanol solution, reflux three times at 65° C. for 3 hours each time, filter, rotary evaporate, recover ethanol, and obtain dark brown thick paste.
[0020] Step 2: Dissolve the obtained thick paste with hot water, adjust the pH value to 10, centrifuge the obtained solution, and take the supernatant. Put the obtained solution on a D101 macroporous resin column, and use a 20% to 60% ethanol aqueous solution for gradient elution, collect 60% of the eluate, and rotary evaporate to obtain a yellow-green powder. The sample is detected by HPLC, and the flavonoid content is 54.3%. .
Embodiment 2
[0022] Step 1: Put 200g of chickpea powder crushed to 0.5-5mm in a round bottom flask, add 1000ml of petroleum ether, heat to a slight boil and reflux for 1h, collect the chickpea powder by suction filtration, add 1000ml of petroleum ether and reflux for 1h, repeat three times. The obtained defatted chickpea powder was dried, added 2400ml of 80% ethanol solution, refluxed at 70°C for 3 times, each time for 3 hours, filtered, rotary evaporated, recovered ethanol, and obtained dark brown thick paste.
[0023] Step 2: Dissolve the obtained thick paste with hot water, adjust the pH value to 10, centrifuge the obtained solution, and take the supernatant. Put the obtained solution on a DS-401 macroporous resin column, and use 20% to 60% ethanol aqueous solution gradient elution, collect 50% of the eluent, and rotary evaporate to obtain a yellow-green powder. The sample is detected by HPLC, and the flavonoid content is 53.2%.
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