Radix ginseng and radix angelicae sinensis blood-nourishing tablet traditional Chinese medicine preparation and preparation and detection methods thereof
A technology for traditional Chinese medicine preparations and detection methods, which is applied in pharmaceutical formulations, drug combinations, blood diseases, etc., can solve problems such as high requirements for particle size and uniformity, increased production costs, and increased difficulty in granulation and tableting.
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Embodiment 1
[0059] 1. Preparation of extract A: Weigh 50g of ginseng, 200g of Astragalus membranaceus, and 50g of Ligustrum lucidum, respectively, and make 3 copies in parallel, and compile them into 1 to 3 experiment numbers, and extract 3 times with 80% ethanol under reflux, and the amount of alcohol added is the mass of medicinal materials respectively 8 times, 6 times, 4 times of that, every 2 hours, collect the extract, measure the amount of dry paste, ginsenoside Re, ginsenoside Rg1, and privetin component content, the experimental results are shown in Table 1. Combine the extracts, filter, recover ethanol under reduced pressure at -0.04Mpa and 70°C, and concentrate to an extract with a relative density of 1.10 to 1.15, which is the density at 60°C.
[0060] Table 1 Statistical table of the experimental results of extracting ginseng, astragalus, and privet lucidum
[0061]
[0062] 2. Preparation of extract B: Weigh 50g of medlar and 50g of oyster respectively, 3 parts each, and ...
Embodiment 2
[0073] 1. Preparation of extract A: feed intake according to 300 times of the prescription amount, reflux extraction with 80% ethanol for 3 times, the first addition of ethanol is 8 times the quality of the medicinal material, and extract for 2 hours; the second addition of ethanol is the medicinal material 6 times the mass, extract for 2 hours; the third addition of ethanol is 4 times the mass of medicinal materials, extract for 2 hours; combine the extracts, filter, and decompress the extracts at 70°C to a thick paste (111.8kg), relative density It is 1.10 to 1.15 (60°C).
[0074] 2. Preparation of extract B: Feed 300 times the amount of the prescription, extract twice by reflux of tap water, add 8 times the quality of the medicinal material for the first time, and extract for 2 hours; 6 times, extract for 2 hours; combine the extracts, filter, and concentrate under reduced pressure at 70°C to a thick paste (60.4kg), with a relative density of 1.10-1.15 (60°C).
[0075]3. P...
Embodiment 3
[0081] 1. The HPLC method determination of the privetin component
[0082] (1) Source and purity inspection of the reference substance: privetin reference substance (batch number: 111926-201404, for content determination, purchased from China National Institute for Food and Drug Control). The content determined by HPLC normalization method is 97.30%.
[0083] Selection of measurement wavelength: take the privetin reference substance solution, and use a UV-visible spectrophotometer to scan and measure from the wavelength range of 200 to 400nm. The scanning results showed that tervinetin had the maximum absorption at the wavelength of 224nm, therefore, it was determined that 224nm was the detection wavelength for detecting tervinetin.
[0084] Chromatographic conditions: chromatographic column: AgilentXDB-C18 column, 250×4.6mm, 5μm; mobile phase: methanol-0.8% phosphoric acid solution (35:65); detection wavelength is 224nm; column temperature: 30°C. Under these conditions, the...
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