A kind of mole cricket extract and its extraction method
An extraction method and extraction technology, applied in the field of mole cricket extract and its extraction, can solve the problems of insignificant inhibition, complicated extraction process, and high cost, and achieve the effect of obvious inhibition, simple extraction process, and low cost
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Embodiment 1
[0027] Take 100 g of the pulverized dry medicinal powder of mole crickets, extract three times with 800 mL of petroleum ether (boiling range is 60-90 ° C) under reflux, and concentrate under vacuum at 60 ° C until there is no solvent smell, and the step yield is about 25%. It was then dissolved in 6 times the volume of 70% acetone aqueous solution, and then placed in the refrigerator for 12 hours. The lower layer solution was taken out and concentrated under reduced pressure at 60°C. The yield in this step was 25%; the total yield calculated by medicinal materials was 6.25%. . The obtained extract was subjected to in vitro inhibition test against glioma cells U87.
Embodiment 2
[0043] Take 100 g of the pulverized dry medicinal powder of mole crickets, extract three times with 600 mL of cyclohexane under reflux, and concentrate under vacuum at 60° C. until there is no solvent smell. The yield in this step is about 25%. It was then dissolved in 4 times the amount of 80% acetone aqueous solution, and then placed in the refrigerator for 10 hours. The lower layer solution was taken out and concentrated under reduced pressure at 60 ° C under vacuum. The yield of this step was about 20%, and the obtained extract was subjected to anti-brain In vitro inhibition assay of glioma cells U87.
Embodiment 3
[0045] Take 100 g of the pulverized dry crude medicinal powder of mole crickets, extract 4 times with 1000 mL of hexane under reflux, and concentrate under vacuum at 60° C. until there is no solvent smell. The yield in this step is about 25%. It was then dissolved in 8 times the amount of 60% acetone aqueous solution, and then placed in the refrigerator for 12 hours. The lower layer solution was taken out and concentrated under reduced pressure at 60 ° C under reduced pressure. The yield of this step was about 22%. The obtained extract was subjected to anti-brain In vitro inhibition assay of glioma cells U87.
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