A method for detecting flavonoid components in peony leaves
A technology of peony leaves and flavonoids, which is applied in the field of research on components of peony leaves, achieves the effects of high accuracy, high sensitivity, and simple operation steps
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[0028] (1) Preparation of flavonoid extract: grind peony leaves into peony leaf powder under freezing conditions, mix the peony leaf powder with alcohol solution to obtain a mixture containing peony leaves, and then process 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;
[0029] (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;
[0030] (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
[0031] (4) Identifying the struc...
Embodiment 1
[0049] Grind 13 parts of fresh peony leaves into powder under liquid nitrogen, weigh 300 mg, add 900 μL of 80% methanol solution containing 0.1% formic acid to extract the flavonoid components in peony leaves, vortex for 1 min to mix, and ultrasonically Extract for 30 minutes, 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 a 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:
[0050] The chromatographic conditions are: mobile phase: solvent A is a mixed solution of acetonitrile and water containing 0.1% volume formic acid, the volume rat...
Embodiment 2
[0063] Embodiment 2 is basically the same as Embodiment 1, the difference is:
[0064] 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.
[0065] A total of 29 main flavonoid...
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