Fat-reducing medicine and preparation method and application thereof
A drug and lipid-lowering technology, applied in drug combinations, pharmaceutical formulas, plant raw materials, etc., can solve the problems of lack of ideal drugs for ALD, unsatisfactory short-term curative effect of ALD, liver toxicity, etc., to inhibit liver cell free radical damage and improve Lipid metabolism, blood lipid lowering effect
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preparation example Construction
[0024] (1) Preparation of reference substance solution: Accurately weigh 5 mg of ginsenoside Rg1, paeoniflorin, salvianolic acid B, and puerarin, respectively, put them in a 50ml volumetric flask, add methanol to dissolve them and set the volume to the mark, mix well, and It is the reference substance solution of ginsenoside Rg1, paeoniflorin, salvianolic acid B and puerarin.
[0025] (2) Preparation of the mixed reference substance solution: Accurately weigh 5 mg of ginsenoside Rg1, paeoniflorin, salvianolic acid B, and puerarin respectively, put them in a 50ml volumetric flask, add methanol to dissolve them and set the volume to the mark, and mix well , which is the mixed reference solution.
[0026] (3) Preparation of the test solution: Accurately weigh 50 mg of the obtained extract, place it in a 100 ml volumetric flask, add an appropriate amount of methanol, ultrasonicate for 30 minutes, let cool to room temperature, dilute methanol to volume, and filter with a 0.45 μm mi...
Embodiment 1
[0029] Get Radix Notoginseng 2kg, Ginkgo Leaf 3kg, Radix Puerariae 2kg, Salvia miltiorrhiza 3kg, Radix Paeoniae Rubra 2kg by proportioning, pulverize, mix evenly, use 168L 70% (volume concentration) ethanol percolation, percolation time is 16~17 hours; Collect percolation solution, concentrated under reduced pressure at 55°C, dried, pulverized, added with 0.2 kg of versicolor glycopeptide, mixed evenly, and obtained.
[0030] HPLC detects that its index component mass fraction is, ginsenoside Rg 1 0.7%, puerarin 0.9%, salvianolic acid B 1.2%, paeoniflorin 1.8%.
Embodiment 2
[0032] According to the ratio, take 2kg of decoction pieces Panax notoginseng, 2kg of ginkgo leaves, 4kg of kudzu root, 2kg of salvia miltiorrhiza and 4kg of red peony, mix well, and percolate with 168L 65% (volume concentration) ethanol, and the percolation time is 16 to 17 hours; collect the percolation liquid , Concentrate at 70°C until there is no alcohol smell, add water to 140L, centrifuge to remove the precipitate, and take the supernatant.
[0033] Adsorb 14L HPD-100 type macroporous adsorption resin on the obtained liquid, wash away impurities with 42L pure water, and elute effective parts with 56L 50% (volume concentration) ethanol solution, and the elution rate is 28L / hour.
[0034] Collect the eluent, concentrate under reduced pressure at 70°C, dry, pulverize, add 0.8 kg of versicolor glycopeptide, mix well, and obtain.
[0035] HPLC detects that its index component mass fraction is, ginsenoside Rg 1 1.3%, puerarin 1.7%, salvianolic acid B 3.0%, paeoniflorin 3.6%....
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