Method for extracting alpha-glucosidase restraining agent effective ingredient from plants
A technology of glucosidase and active ingredients, which is applied in the preparation of Chinese herbal medicines and the fields of chemical and chemical engineering, can solve the problems of no α-glucosidase inhibitors, and achieve the effects of no pollution to the environment, simple process and high purity
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Embodiment 1
[0014] In the present embodiment, the extraction process and steps of α-glucosidase inhibitor are as follows:
[0015] (1) First, crush 2g of plant leaves; put a 250ml beaker and add 50% ethanol solution at a ratio of 1:40 (g / ml), shake at room temperature for 3h; centrifuge at 8000rpm / min for 20min at room temperature, and harvest the supernatant; plant residues are added 50% ethanol solution, repeat the extraction 3 times; combine the 3 extractions;
[0016] (2) Recover the ethanol solution with a rotary evaporator to obtain 0.72g of solid, add 100ml of hot water for redissolving; add ethyl acetate solution for extraction at a ratio of 1:1, collect 85ml of the aqueous phase; in the harvest solution at a ratio of 1:1 Add n-butanol solution for extraction, collect the water phase part, spin dry to obtain 0.48g solid, 5ml hot water redissolving for use;
[0017] (3) MARC (macroporous adsorption resin) chromatography on the above sample (filler height 35cm, column diameter 2.6c...
Embodiment 2
[0020] The process of the present embodiment 2 is exactly the same as that of the embodiment 1, and its steps are as follows:
[0021] (1) First, crush 2g of plant leaves; put a 250ml beaker and add 50% ethanol solution at a ratio of 1:40 (g / ml), shake at room temperature for 3h; centrifuge at 8000rpm / min for 20min at room temperature, and harvest the supernatant; plant residues are added 50% ethanol solution, repeat the extraction 3 times; combine the 3 extractions;
[0022] (2) Recover the ethanol solution with a rotary evaporator to obtain 0.81g of solid, add 100ml of hot water for redissolving; add ethyl acetate solution for extraction at a ratio of 1:1, collect 89ml of the aqueous phase; in the harvest solution at a ratio of 1:1 Add n-butanol solution for extraction, collect the water phase part, spin dry to obtain 0.52g solid, redissolve in 5ml hot water for use;
[0023] (3) MARC (macroporous adsorption resin) chromatography on the above sample (filler height 35cm, col...
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