Method for determining oleanolic acid content and ursolic acid content in patrinia heterophylla by ultra-high performance liquid chromatography
An ultra-high-efficiency liquid phase and oleanolic acid technology, applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve the problems of shortened column life, slow detection speed, difficult to clean, etc., to ensure safety and effectiveness , Fast detection speed and strong specificity
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Embodiment 1
[0038] (1) Preparation of reference solution:
[0039] Accurately weigh oleanolic acid (National Institute for Food and Drug Control, 110709-201607, the content is 91.7%, without drying before use) and ursolic acid (National Institute for Food and Drug Control, 110742-201622, content Based on 94.7%, without drying treatment before use) About 100 mg of the reference substance, placed in a 10 ml volumetric bottle, diluted with an appropriate amount of methanol to dissolve, and diluted to the mark with it, shaken well, and respectively prepared with a concentration of 10 mg / mL of oleanolic acid and ursolic acid reference substance stock solution.
[0040] Precisely measure 5, 10, 20, 50, 100, 500, and 1000 μL of oleanolic acid and ursolic acid reference substance stock solutions, put them in 10 mL measuring bottles, dilute to the mark with methanol, and shake well to As the standard solution of oleanolic acid and ursolic acid respectively.
[0041] (2) Preparation of sample so...
Embodiment 2
[0051] It is basically the same as steps (1) to (4) in Example 1, only the following changes are made: the chromatographic conditions are: use 4.6×100 mm, 2.6 μm phenomenonex Kinetex chromatographic column; methanol-0.1% with a volume ratio of 85:15 Aqueous ammonium acetate solution was used as the mobile phase at a flow rate of 0.2 mL / min; detected by an ultraviolet detector with a detection wavelength of 210 nm; column temperature: 30°C; injection volume 20 μL.
Embodiment 3
[0053] It is basically the same as steps (1) to (4) in Example 1, only the following changes are made: the chromatographic conditions are: use 4.6×100 mm, 2.6 μm phenomenex Kinetex chromatographic column; methanol-0.5% with a volume ratio of 85:15 Ammonium acetate aqueous solution was used as the mobile phase at a flow rate of 1.0 mL / min; detected by an ultraviolet detector with a detection wavelength of 210 nm; column temperature: 35°C; injection volume 15 μL.
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