Preparation method of mulberry leaf alkaloids and application of prepared mulberry leaf alkaloids
A technology of mulberry leaf alkaloids and medicines, applied in the field of alkaloid extraction, can solve the problems of secondary pollution of organic solvents, low alkaloid purity, and low relative content of alkaloids
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[0040] The invention provides a preparation method of mulberry leaf alkaloids, which comprises the following steps: 1) mixing mulberry leaves with an aqueous ethanol solution according to a solid-liquid ratio of 1 g: (15-26) mL to obtain a mixture;
[0041] 2) The mixture obtained in step 1) is ultrasonically filtered to obtain a filtrate; the power of the ultrasonic wave is 720-900W;
[0042] 3) Concentrating the filtrate obtained in step 2) to obtain a concentrate;
[0043] 4) Purify the concentrated solution obtained in step 3) through a column to obtain mulberry leaf alkaloids; the column for column purification includes 732 type cation exchange resin and D101 type macroporous adsorption resin.
[0044] In the preparation method of the mulberry leaf alkaloid of the present invention, the mulberry leaf and the aqueous ethanol solution are mixed according to a solid-liquid ratio of 1 g: (15-26) mL to obtain a mixture. The mulberry leaves in the present invention are prefera...
Embodiment 1
[0061] Weigh the mulberry leaf powder, add it into 60% ethanol aqueous solution according to the ratio of material to liquid 1:20 (g:mL), put it in an ultrasonic cleaning machine with an ultrasonic frequency of 800W for 10min, and vacuum filter (qualitative filter paper, medium speed, Φ9cm ) was filtered to obtain the filtrate, and the combined filtrate was extracted 3 times, evaporated and concentrated to a volume ratio of 2:1 by rotating at 80°C (rotating speed: 100rpm) for later use.
[0062] The obtained concentrated solution was first purified by passing through a D101 macroporous adsorption resin column, and the effluent was collected for future use.
[0063] Add 4 volumes of absolute ethanol to the effluent, and precipitate polysaccharide overnight at 4°C. The filtrate was centrifuged at 4°C, 5000r / min for 10min, the precipitate was discarded to obtain the supernatant, and the supernatant was concentrated by rotary evaporation (rotating at 100rpm) to remove ethanol unti...
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