Medicinal composition for regulating blood fat, prepn. method and use thereof
A technology for regulating blood lipids and compositions, applied in the field of pharmaceutical compositions and their preparation, to achieve the effects of scientific and precise drug compatibility, small dosage of drugs, and retention of active ingredients
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Embodiment 1
[0035] Embodiment 1: the preparation of pharmaceutical composition capsule of the present invention:
[0036] Hawthorn 2000g Alisma 1500g Atractylodes macrocephala 1500g Red yeast rice 1000g
[0037] Add 6 times the amount of 80% ethanol to the above four medicinal materials, and reflux and extract three times, each time for 1.5 hours. Filtrate, recover ethanol from the filtrate to a relative density of 1.00-1.03 (60°C), concentrate under reduced pressure to a relative density of 1.20-1.25 (60°C), add 4-5 times the amount of water, let stand, centrifuge, and separate the precipitate. dry. The supernatant is passed through the pretreated macroporous resin column, washed with water until colorless, and then washed with 70% ethanol until colorless, the eluate is collected, the ethanol is recovered, concentrated into a thick paste, dried, and combined with the above dried centrifugal precipitate , pulverized, sieved, added an appropriate amount of micropowder silica gel, mixed e...
Embodiment 2
[0039] Embodiment 2 The content determination of the quality control index component of the pharmaceutical composition of the present invention:
[0040] Take the content of 10 capsules of this product, mix well, take 0.2g, accurately weigh, put in a 100ml Erlenmeyer flask, add 20ml of ether, ultrasonicate for 10 minutes (cold water bath), filter, wash the precipitate twice with ether, 20ml each time, the filtrates were combined, evaporated to dryness, and the residue was dissolved by adding absolute ethanol and transferred to a 10ml measuring flask, and diluted to the mark, as the test solution. Take another ursolic acid reference substance, add absolute ethanol to make a solution containing 0.3mg per 1ml, as the reference substance solution. Test according to thin-layer chromatography (Appendix VI B of Chinese Pharmacopoeia in 2000), draw 5 μl of the test solution, 5 μl and 10 μl of the reference solution, respectively cross points on the same silica gel G thin-layer plate, ...
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Abstract
Description
Claims
Application Information
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