Method for extracting active ingredients of Euphorbia fischeriana and diterpenoid medicament prepared by active ingredients
A technology of Euphorbia chamaejasma and its active ingredients, which is applied in the field of extracting active ingredients of Euphorbia chamaejasma, can solve the problems of low extraction rate of diterpenoids and difficulty in improving the therapeutic effect, and achieve simple economy, large processing capacity, and easy industrialization Effect
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Embodiment 1
[0022] Take the root of Euphorbia chamaejasma, dry it in the shade, grind it into 14-24 mesh powder, put it into a supercritical carbon dioxide extraction kettle, extraction conditions: 25 MPa, 55°C, supercritical carbon dioxide fluid flow rate 100:10% (v / v ) ratio to add entrainer absolute ethanol. Separation tank separation: 8 MPa, 40°C. Extract according to the above conditions for 4 h, and collect the extract separated from the separation tank.
[0023] Ethanol was recovered from the extract under reduced pressure until there was no distillate and a white viscous substance was obtained. This white viscous thing is made into suspension with sherwood oil: ethyl acetate (75:25), and this liquid flows through the macroporous adsorption resin column (diameter 5cm, length 100cm), to about 1 / 3 column volume of the colored layer. First use petroleum ether:ethyl acetate (75:25) to elute 3 times column volume at a flow rate of 3BV / h; Column volume, collect the eluate containing...
Embodiment 2
[0029] Take the root of Euphorbia chamaejasma, dry in the shade, and crush it into 14-24 mesh powder. Get the same amount of medicinal powder and put it into a supercritical carbon dioxide extraction kettle, and extract according to the supercritical carbon dioxide extraction conditions listed in Table 1. The supercritical carbon dioxide fluid extraction volume is 8 times the volume of the extraction kettle. Carry out macroporous resin separation then, the eluent containing compound jolkinolide B component in the obtained product, it is named as compound 1, contains the eluent of compound 17-hydroxyjolkinolide B component, is named as compound 2, contains The eluate of component A of compound 17-hydroxyjolkinolide, which is named as compound 3, is listed in Table 1 relative to the content of the drug powder.
[0030] Table 1
[0031]
Embodiment 3
[0033] The preparation of medicine of the present invention:
[0034] The three enriched products in Example 1 were combined according to the following ratios to form the diterpene drug ETD516 (1).
[0035] Jolkinolide B enrichment: 17-hydroxyjolkinolide B enrichment: 17-hydroxyjolkinolide A enrichment==25:30:45
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