Method for detecting aster donoryzicola or aster marginata
A detection method and technology for aster, applied in the field of analysis of natural plant medicines, can solve the problems of unguaranteed safety and effectiveness of clinical medicines, confusion of the basis, and unfavorable control and evaluation of the overall quality of aster medicinal materials.
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[0024] Example 1 Detection method of Aster edulis and Aster ciliate
[0025] Chromatographic conditions:
[0026] Chromatographic column: (2.1×100 mm, 1.8 µm) ACQUITY UPLC R HSS C18; mobile phase: acetonitrile (A)-0.1% aqueous formic acid (B); gradient elution, 0-5 min, 10%-12% A; 5~19 min, 12%~16% A; 19~26 min, 16%~24% A; 26~28 min, 24%~24% A; 28~30min, 24%~30%A; 35~45 min, 30%~45% A; volume flow rate 0.2 mL.min-1; column temperature 35°C; detection wavelength 325 nm
[0027] Extraction and Separation
[0028] Weigh 300g each of Aster dongeruo and Aster phyllosa, add 1000ml 70% ethanol to reflux to extract
[0029] Take 3 times, the time is 1h, and concentrate under reduced pressure to obtain the extract. Add distilled water to dissolve, then pass through HP-20
[0030] Macroporous resin separation, first eluted with 15% ethanol, discarded, then eluted with 70% ethanol, collected eluate,
[0031] Concentrate and dry to obtain 14.84g and 21.79g of the crude extracts of A...
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