Detection method of caesalpinia decapetala cold mixture
A technology of Yunshi Ganmao mixture and detection method, which can be applied to antiviral agents, measuring devices, drug combinations, etc., can solve the problems of inconvenient transportation and carrying, unstable quality, and poor taste of the original dosage form.
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Embodiment 1
[0110] Yunshi Ganmao Mixture is prepared from the following raw material weight ratios:
[0111]
[0112] The above-mentioned Yunshi Ganmao mixture is prepared according to the following method: extract the volatile oil from the above four medicinal materials and ginger, distill and collect the aqueous solution in a separate device, decoct the medicinal residue and the other three flavors such as Yunshipi with water for three times, the first time for 2 hours, The second and third times are 1.5 hours each, and the decoctions are combined and filtered. Combine the filtrate with the distilled aqueous solution, concentrate to a clear paste with a relative density of 1.18-1.22 (50°C), add ethanol until the alcohol content is 75%, mix well, let stand for 24 hours, filter, and recover ethanol from the filtrate. Add brown sugar, sodium benzoate, ethyl p-hydroxybenzoate, polysorbate 80 and ginger volatile oil, mix well, add water to the specified amount, let it stand for 24 hours, ...
Embodiment 2
[0129] Example 2. Yunshi Ganmao Mixture is prepared from the following raw material weight ratios:
[0130] The prescription and preparation method of Yunshi Ganmao mixture are as in Example 1.
[0131] Properties of this product: This product is a brownish-red liquid; the air is slightly gingery, and the taste is slightly sweet and then bitter and astringent.
[0132] The detection method of Yunshimao mixture of the present invention comprises the determination of (±) prohematoxylin B content in Yunshipi.
[0133] In the detection method of aforementioned Yunshimao mixture, the content determination of (±) prohematoxylin B in Yunshipi is determined by Chinese Pharmacopoeia HPLC method, and the specific method is as follows:
[0134] ① Chromatographic conditions and system suitability test
[0135] Chromatographic column: Shimadzu GL Inertsil ODS-SP C18 column: 4.6×250mm, 5μm; ZORBAX EclipsePlus C18: 4.6×250mm, 5μm; mobile phase: acetonitrile: 0.2% acetic acid = 10~20: 80~9...
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