Plant extract composition for preventing and treating lipidmetabolic disorder and preparation method thereof
A technology of plant extracts and lipid metabolism disorders, applied in drug combinations, metabolic diseases, plant raw materials, etc., can solve the problems that affect the stability of the clinical efficacy of the product, the compliance of patients is not ideal, and the active ingredients cannot be purified. , achieve safety without obvious side effects, controllable product quality, reduce the effect of preparation quality and safety
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Embodiment 1
[0035] The preparation of embodiment 1 SHCE
[0036] One, the preparation of Panax notoginseng total saponins extract
[0037] (1) Panax notoginseng saponins extract
[0038]Weigh 10 kg of Panax notoginseng medicinal material, pulverize it, and reflux extraction with 75% ethanol of 8 times, 8 times and 6 times the amount of the medicinal material, respectively, for 3 times, 2 hours each time, and filter the combined extracts with a 200-mesh filter cloth, and combine the filtrates. Recover the ethanol and make the concentration of the ethanol extraction part 1ml equivalent to 1g crude drug concentrate (1.9 L); absorb on a macroporous resin column, the macroporous resin is HPD-100 of the polystyrene weakly basic anion exchange resin series, press 1 Add 1.5L of concentrated solution to a macroporous resin column for adsorption on kg resin, wash with water until the eluate is nearly colorless, then elute with 4.5 L of 85% ethanol at a flow rate of 10 ml / min, and elute until t...
Embodiment 2
[0083] Example 2 Effect of SHCE on gene expression and activity of key enzymes in blood lipid metabolism
[0084] 1.1 Effects on gene expression and activity of hepatic lipase (HL) enzyme and cholesterol 7-α-hydroxylase (CYP7A1) in hepatocytes
[0085] Cultivate L-O2 human normal liver cells according to the routine. After the cells are fused, add various concentrations of SHCE and FTZ. After continuing to cultivate for a certain period of time, collect the cells to make a cell homogenate, use the HL detection kit, and use the colorimetric method The enzyme activities of HL and CYP7A1 were detected, the effects of the above-mentioned different concentrations of SHCE on the enzyme activities of HL and CYP7A1 were studied, and the enzyme activities of HL and CYP7A1 in liver cells under the action of different concentrations of SHCE were compared. In addition, total RNA in hepatocytes was extracted with Trizol reagent, and the expression of CYP7A1 and HL enzyme genes in hepatoc...
Embodiment 3
[0101] Example 3 Effect of SHCE on Experimental Rat Hyperlipidemia
[0102] Experimental animals: SD rats, SPF grade, male, body weight 200±20 g.
[0103] Experimental method: After one week of adaptive feeding, the rats were randomly divided into normal control group and model-making group according to body weight, of which 10 in the normal control group were fed with basic feed; 80 in the model-making group were fed with high-fat feed for 2 weeks, Orbital blood was taken to measure blood lipids, and those with significantly higher blood lipids were selected as rats with successful hyperlipidemia modeling.
[0104] Those whose blood TC value was higher than 2.5mmol / L were included in the experiment, and hyperlipidemia rats were divided into hyperlipidemia model group, each extract group and positive drug simvastatin (20mg / kg body weight·d) group according to the blood lipid level. Group 10. The normal control group and the hyperlipidemia model group were given equal volum...
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