Processed rhubarb or/and raw rhubarb detection method
A detection method, the technology of raw rhubarb, applied in the detection field of processed rhubarb or/and raw rhubarb, can solve the problems of unfavorable detection cost, environmental protection, high price of acetonitrile, large amount of acetonitrile, etc., to achieve good separation and save Detection cost, effect of reducing operation steps
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Embodiment 1
[0076] The processing method of embodiment 1 rhubarb of the present invention
[0077] Take raw rhubarb, add 30ml of yellow rice wine and 70ml of water for every 100g, mix well, moisten for 4 hours, and the yellow rice wine is completely absorbed by the medicinal materials. Steam in a pressure cooker at 120°C for 3 hours, take it out, dry at a low temperature of 60°C, and repeat the operation twice to obtain processed rhubarb.
[0078] Steaming in the present invention refers to the steaming method described in appendix II D of "Chinese Pharmacopoeia" 2005 edition.
[0079] The raw rhubarb described in the present invention is the dry root and rhizome of Rheum officinale Bail., Rheum palmatum L. or Rheum tanguticum Maxim.ex Balf.
[0080] The rice wine described in the present invention is obtained by purchasing commercially available products, such as Sichuan Yilong Yinming Rice Wine Co., Ltd. (executive standard: GB / T 13662).
Embodiment 2
[0081] The processing method of embodiment 2 rhubarb of the present invention
[0082] Add 30ml rice wine and 70ml water per 100g of raw rhubarb, mix well, moisten for 4 hours without leaving any remaining water, press in a pressure cooker at 120°C for 6h, take it out, and dry at 60°C to obtain the product.
Embodiment 3
[0083] The quality detection method of embodiment 3 nine system rhubarb of the present invention
[0084] (1) Preparation of sample solution:
[0085] Precisely weigh about 0.5g of the nine-made rhubarb sample powder (passed through a No. 4 sieve), add 25ml of methanol, weigh, soak for 12 hours, and ultrasonically for 30 minutes, let the extract cool to room temperature, make up the weight, filter, and take the subsequent filtrate as the test sample solution;
[0086] (2) Preparation of reference solution:
[0087] Dissolve chrysophanol with methanol, microfilter, and the filtrate is used as a reference solution, containing 16 μg of chrysophanol per 1 ml;
[0088] (3) Chromatographic conditions:
[0089] Column: Kromasil C 18 (250×4.6mm, 5μm); mobile phase: A: methanol, B: 0.1% phosphoric acid water, gradient elution program: from 0 to 5min, A phase from 5% to 20%, B phase from 95% to 80% ;5~15min, A phase is 20%~35%, B phase is 80%~65%; 15~23min, A phase is 35%~40%, B ph...
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