Baccharis dracunculifolia propolis quality control method
A quality control method and technology of Bacchus chrysanthemum, which are applied in the directions of measuring devices, instruments, scientific instruments, etc., can solve the problems of uneven quality of Bacchus type propolis, lack of quality evaluation methods of Bacchus type propolis, and the like, and achieve sensitivity. High, high feasibility, good separation effect
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Embodiment 1
[0025] Accurately weigh 10 mg of the standard product of atipirin C, and dilute it to 10 mL with methanol to prepare the standard stock solution of atipirin C; absorb a certain amount of standard stock solution of atipirin C as needed, and dilute it with methanol Dilute to volume and prepare standard working solutions of 0.1, 02, 0.3, 0.4, 0.5, 0.6 mg / mL. They were filtered through microporous membranes and analyzed by HPLC. Draw the standard curve of atipirin C.
[0026] Take a certain amount of test samples for freezing, pulverization and mixing, take 0.25 g Dionysus propolis respectively, the ratio of solid to liquid is 1:15, ultrasonic for 30 min, extract three times, filter and rotary evaporate to obtain the extract, and then use Pure methanol was ultrasonically dissolved to a volume of 50 mL, filtered through a microporous membrane, and determined by HPLC.
[0027] The conditions of the liquid chromatograph are: the flow rate is 1.0 mL / min, the detection wavelength is ...
Embodiment 2
[0040] Take 0.3 mg / mL standard working solution, filter it with a microporous membrane, and analyze it by HPLC.
[0041] A certain amount of Shandong poplar-type propolis and poplar gum were frozen, crushed and mixed, and 10 g were taken respectively, according to the ratio of solid to liquid 1:15, ultrasonically extracted for 3 times, filtered, and rotary evaporated to obtain the extract. Take 0.25 g of the extract respectively, dissolve it in ultrasonic with pure methanol, filter it through a microporous membrane, and measure it by HPLC.
[0042] The conditions of the liquid chromatograph are: the flow rate is 1.0mL / min, the detection wavelength is 310 nm, the injection volume is 2 μL, the chromatographic column is Sepax HP-C18 (4.6×150mm, 5 μm) or equivalent chromatographic column, and the column temperature is is 30°C. The mobile phase is pure methanol and 1% acetic acid aqueous solution with a volume ratio of 1% for gradient elution by volume ratio. The elution program i...
Embodiment 3
[0044] Take 0.3 mg / mL standard working solution, filter it through a microporous membrane, and analyze it by HPLC.
[0045] A certain amount of Australian Eucalyptus propolis and Taiwan Macaranga spp. were frozen and pulverized, 10 g were taken respectively, and the material-to-liquid ratio was 1:15, ultrasonicated for 30 min, extracted three times, filtered, and rotary evaporated to obtain extracts. Take 0.25 g of the extract respectively, dissolve it in ultrasonic with pure methanol, filter it through a microporous membrane, and measure it by HPLC.
[0046] The conditions of the liquid chromatograph are: the flow rate is 1.0mL / min, the detection wavelength is 310 nm, the injection volume is 2 μL, the chromatographic column is Sepax HP-C18 (4.6×150mm, 5 μm) or equivalent chromatographic column, and the column temperature is is 30°C. The mobile phase is pure methanol and 1% acetic acid aqueous solution with a volume ratio of 1% for gradient elution by volume ratio. The elutio...
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