Method of preparing cortex mori radicis extractive with glycosidase restraint function
A Morus alba extract and extract technology, applied in the field of traditional Chinese medicine extract and its preparation, can solve the problems of unsuitability for industrial production, complex preparation process, and low content of active ingredients
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Embodiment 1
[0047] After cutting 100g of Morus alba medicinal material, stir and extract three times at 35°C, the amount of water added is 8, 6, and 6 times the weight of the medicinal material, and the extraction time is 3, 2, and 1 hour respectively. The three extracts are combined, and the pressure is reduced at 60°C Concentrate, 200ml of the concentrated solution is centrifuged on an activated carbon column (activated carbon model is GH-15, the dosage is 100 grams, wet packing), the temperature of the upper column liquid is 50°C, and the activated carbon column is eluted with water until the washing liquid is clear (indrin Ketone reaction is negative) change to 15% ethanol for elution and start to receive the eluent, use 1-naphthol reagent to qualitatively detect the total sugar, end the elution when the Molish reaction disappears, 15% ethanol eluent 60 ° C Concentrated under reduced pressure, and the concentrated solution was dried under reduced pressure at 50° C. to obtain 3.5 g of C...
Embodiment 2
[0049] After cutting 100g of Morus alba medicinal material, stir and extract three times at 50°C, the amount of water added is 7, 5, and 5 times the weight of the medicinal material respectively, and the extraction time is 2, 1, and 1 hour respectively. The three extracts are combined and reduced at 60°C Concentrate, add 900ml of 95% ethanol to 300ml of the concentrated solution, place it overnight at room temperature, evaporate the ethanol from the supernatant, adjust it to 200ml of aqueous solution and put it on an activated carbon column (the model of activated carbon is GH-15, the dosage is 50 grams, and the column is wet-packed). The temperature of the upper column liquid is 30°C, and when the activated carbon column is eluted with water until the washing liquid is clear (ninhydrin reaction is negative), replace it with 20% ethanol for elution and start to receive the eluent, and use 1-naphthol reagent to qualitatively detect the total Sugar, when the Molish reaction disap...
Embodiment 3
[0051] 100g of Morus Alba medicinal material is cut, extracted three times with 30% ethanol under reflux, the amount of solvent is 7, 6, 5 times of the weight of medicinal material respectively, the extraction time is 2, 1, 1 hour respectively, and the three extracts are combined, Concentrate under reduced pressure at 60°C, centrifuge 300ml of the concentrated solution onto an activated carbon column (the type of activated carbon is GH-1, the dosage is 100 grams, wet packing), the temperature of the liquid on the column is 45°C, and the activated carbon column is eluted with water until the washing solution is clear When the ninhydrin reaction is negative, change to 30% ethanol for elution and begin to receive the eluate, use 1-naphthol reagent to qualitatively detect the total sugar, end the elution when the Molish reaction disappears, and 30% ethanol elution The solution was concentrated under reduced pressure at 60° C., and the concentrated solution was dried under normal pr...
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