Pharmaceutical composition for reducing blood sugar as well as preparation method and application of pharmaceutical composition
A composition and blood sugar-lowering technology, applied in the direction of drug combination, pharmaceutical formula, medical preparations containing active ingredients, etc., to achieve the effects of promoting hematopoietic function, anti-inflammatory and anti-tumor immunity, and regulating gastric contraction
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Embodiment 1
[0024] Embodiment 1 polysaccharide extraction
[0025] Polygonatum multiflora, Lycium barbarum, Codonopsis pilosula, and jujube are extracted with the same method to extract polysaccharides. The specific extraction method is as follows:
[0026] (1) Drying: medicinal materials are dried in an oven at 55°C until the water content does not exceed 10%.
[0027] (2) Pulverization: take the dried medicinal material raw material, pulverize and pass through a No. 4 sieve.
[0028] (3) Degreasing and impurity removal: Add 10 times the amount of petroleum ether (boiling range 60-90°C) to the medicinal material powder, shake well, reflux in a water bath at 75°C for 2 hours, suction filter to recover petroleum ether, and evaporate the residue in the filter cake at the same time petroleum ether. After adding 10 times the amount of 95% ethanol solution to the filter cake to reflux for extraction for 1.5 h, the filter residue was collected by suction filtration and dried in an oven at 55°...
Embodiment 2 4
[0033] The hypoglycemic effect of embodiment 2 four kinds of medical material polysaccharides
[0034] (1) Grouping: 200 experimental mice were equally divided into normal group, control group and model group 1-18, with 10 mice in each group.
[0035] (2) Induced model: use drugs to induce mice in the control group and model group 1-18 into a diabetic mouse model, and measure the blood glucose of the mice by taking blood from the tip of the tail and using blood glucose test paper to determine whether the diabetic mouse model is successfully established. The specific method is as follows: after the mice were fasted overnight, the STZ solution (50 mg / kg, STZ dissolved in citric acid buffer, pH 4.2) was intraperitoneally injected the next day. After continuous injection for 5 days, the blood glucose changes of the mice were monitored. After 7 days, the mice with blood glucose concentration ≥ 16.7mmol / L were successfully modeled.
[0036] (3) All mice were given intragastric adm...
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