Method for detecting flavonoids component in peony petals
A technology of peony petals and flavonoids is applied in the research field of peony petal components, which can solve the problems of long operation time, low accuracy and insufficient sensitivity, and achieve the effects of simple operation steps, high precision and high sensitivity.
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[0031] (1) Preparation of flavonoid extract: grind peony petals under freezing conditions into peony petal powder, mix the peony petal powder with alcohol solution to obtain a mixture containing peony petals, and then carry out the mixture in sequence Ultrasonic treatment and centrifugation, collecting the supernatant and removing the precipitate, and then filtering the collected supernatant through a filter membrane to remove solid impurities to obtain a flavonoid extract;
[0032] (2) The chromatographic conditions of the ultra-high performance liquid chromatography, the mass spectrometry conditions of the triple quadrupole time-of-flight tandem mass spectrometer and the setting of the detection wavelength of the diode array detector;
[0033](3) Using ultra-high performance liquid chromatography-diode array detector-triple quadrupole time-of-flight tandem mass spectrometry to detect the flavonoid extract, and obtain the detection results; and
[0034] (4) Identifying the st...
Embodiment 1
[0050] Grind 15 parts of fresh peony petals into peony petal powder under liquid nitrogen, weigh 300 mg, add 1% formic acid by volume, 900 μL of methanol solution with a volume concentration of 80%, extract the flavonoid components in peony petals, and vortex for 1 min Mix well, ultrasonically extract for 30 minutes, and centrifuge at a high speed of 13000r / min for 10 minutes, collect the supernatant and remove the precipitate, then pass the supernatant through a 0.22 μm organic filter to remove solid impurities to obtain flavonoid extract. The obtained flavonoid extract was analyzed by ultra-high performance liquid chromatography-diode array detector-triple quadrupole time-of-flight tandem mass spectrometry. Wherein, the settings of chromatographic conditions, mass spectrometry conditions and diode array detector detection wavelength range are as follows:
[0051] The chromatographic conditions are: mobile phase: solvent A is a mixed solution of acetonitrile and water contain...
Embodiment 2
[0071] Embodiment 2 is basically the same as Embodiment 1, the difference is:
[0072] The chromatographic conditions are: mobile phase: solvent A is a mixed solution of acetonitrile and water containing 0.2% volume formic acid, the volume ratio of water and acetonitrile is 90:10, solvent B is an acetonitrile solution containing 0.2% volume formic acid; flow rate is 0.2mL / min; column temperature is 30°C; injection volume is 4μL; gradient elution conditions: 0-22min, 100% solvent A-72% solvent A, 0% solvent B-28% solvent B; 22-22.5min, 72% solvent A~60% solvent A, 28% solvent B~40% solvent B; 22.5~23min, 60% solvent A~0% solvent A, 40% solvent B~100% solvent B; 23~26.5min, 0 % solvent A, 100% solvent B; 26.5 ~ 27min, 0% solvent A ~ 100% solvent A, 100% solvent B ~ 0% solvent B; 27 ~ 32min, 100% solvent A, 0% solvent B, that is, liquid The gradient elution conditions of phase chromatography were set according to the procedures in Table 1.
[0073] A total of 5 main anthocyani...
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