Objective To establish a novel method for determination of isoxaflutole and its metabolites residues in rice by liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS). Methods With acetic acid acetonitrile solution(1:9,V:V) as the extraction, the test sample were extracted by means of high speed homogenization, cleaned up by primary secondary amine (PSA) and octadecylsilane (ODS). The residues in the extracts were separated on a reversed–phase liquid chromatography with ACQUITY UPLC BEH Phenyl column using a gradient elution program of 1.5% acetic acid (1 mmol/L) ammonium acetate solution and acetonitrile. The residues were determined and confirmed by LC-MS/MS equipped with atmosphere pressure chemical ionization source. Results The calibration curve of isoxaflutole and its metabolites showed a good linearity in the range of 0.0025~1.000 μg/mL with the correlation coefficient of 0.9998~0.9999. The average recoveries of isoxaflutole and its metabolites in spiked samples were in the range of 70.2%~110.6%, and the relative standard deviations (RSD) were between 7.38%~12.84% at spiked levels of 5~200 μg/kg. The limit of detection was 10 μg/kg and 5 μg/kg for the isoxaflutole and its metabolites, respectively. Conclusion This method can be used for the simultaneous determination of isoxaflutole and its metabolites residues in rice.
标题:液相色谱-串质谱法测定大米中异噁唑草酮及代谢物残留量
英文标题:Determination of isoxaflutole and its metabolites residues in rice by liquid chromatography-mass spectrometry/mass spectrometry
作者:
罗佳 辽宁出入境检验检疫局
杨长志 黑龙江出入境检验检疫局
沈睿至 黑龙江出入境检验检疫局
中文关键词:异噁唑草酮及代谢物,液相色谱-串联质谱法,大米,
英文关键词:isoxaflutole and its metabolites,liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS),rice,