Method for determining coumarin and metabolite of coumarin in mouse blood on basis of UPLC (ultra performance liquid chromatography)-orbitrap HRMS (high-resolution mass spectrum)
A technology of high-resolution mass spectrometry and ultra-high performance liquid chromatography, applied in the field of determination of coumarin and its metabolites in mouse blood based on ultra-high performance liquid chromatography-Orbitrap high-resolution mass spectrometry, can solve the problem that cannot give adduct The problem of structure information, poor stability, and low sensitivity of specificity can be solved, and the effect of high sensitivity, good repeatability, and simple pretreatment can be achieved.
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example 1
[0028] 1. Instruments and materials:
[0029] Ultimate ultra-high performance liquid chromatography, Q-Exactive orbitrap high-resolution mass spectrometer (ThermoScientific, USA); Milli-Q Advantage A10 ultrapure water instrument (Millipore, USA); Agilent ZorbaxEclipse XDB-C 18 (2.1×150 mm, 3.5 μm).
[0030] Female mice (SPF grade C57BL / 6, 7±1 weeks old, body weight 17±1 g, provided by Changzhou Cavens Experimental Animal Co., Ltd.). Methanol, acetonitrile (chromatographically pure, Merck, Germany); formic acid (chromatographically pure, Serva, Germany); coumarin (>98%, TRC Canada); 7-hydroxycoumarin, 4-methylumbelliferone, 5-methanone Oxypsoralen (>99%, Aldrich, USA); Sodium Chloride (analytical grade, Zhengzhou Piney Reagent).
[0031] 2. Sample processing: 0.5 h after intraperitoneal injection of CYP2A5 probe drug coumarin solution (100 mg / kg, 1 mL / 100 g body weight) in mice, 0.5 mL of blood was collected from the canthus of the eye and injected into a 1.5 mL centrifuge ...
example 2
[0033] Example 2: As described in Example 1, the analytical method established in this study was used to detect the content of coumarin and its metabolites in the blood of the control group and CYP2A5 enzyme activity-inhibited mice.
[0034] 1. 100 C57BL / 6 mice were randomly divided into the control group and the 5-methoxypsoralen (5-MOP) group, 50 each, and the two groups were randomly divided into 10 groups with 5 mice in each group. And each group corresponds to a same time point. At 9 am every day, the 5-MOP group was given 5-MOP solution (dissolved in corn oil, 25 mg / kg, 1 mL / 100 g body weight) by intragastric administration, while the control group was given an equal volume of normal saline. Administered three times in a row with an interval of 24 hours each time. Twelve hours before the third dose, the mouse chow was removed. Mice had free access to water during the experiment.
[0035] One hour after the last administration, each mouse was injected intraperitoneall...
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