Extraction technology of Lemai particle crude medicines
An extraction process and a technology for raw materials, applied in the field of medicine, can solve problems such as large gaps in effective components, low extraction efficiency, unreasonable processes, etc., and achieve the effects of reducing raw material costs, reducing paste yield, and reducing production costs.
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Embodiment 1
[0023] Embodiment 1 The extraction process of Lemai granule bulk drug of the present invention
[0024] Weigh 160g of salvia miltiorrhiza, 80g of chuanxiong, 80g of safflower, 80g of red peony, 40g of Cyperus cyperi, 40g of woody fragrance, and 20g of hawthorn. Put the above-mentioned crude drug into a decompression extraction tank, add water 10 times the weight of the raw material, soak for 2 hours, then heat to 80°C, then evacuate to boiling, keep boiling for 3 times, each time for 1 hour, combined extraction liquid.
Embodiment 2
[0025] Embodiment 2 The research of Lemai granule raw material extraction process of the present invention
[0026] 1. Determination of salvianolic acid B, ferulic acid and paeoniflorin in medicinal materials
[0027] Referring to the relevant content and methods under the items of Danshen, Chuanxiong, and Chishao in the 2010 edition of "Chinese Pharmacopoeia", the contents of salvianolic acid B, ferulic acid, and paeoniflorin in the medicinal materials used in this experiment were respectively measured.
[0028] 2. Chromatographic conditions for determination
[0029] Stationary phase: LP-C18 (4.6*250mm, 5μm); mobile phase: acetonitrile-0.4% phosphoric acid gradient elution, as shown in the table below. Detection conditions: column temperature 25°C, detection wavelength 235nm, injection volume 10μL.
[0030] Table 1
[0031]
[0032] 3. Determination of dry paste rate
[0033] Take 30mL of the extract and place it in an evaporating dish with constant weight (M 1 ), dr...
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