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作 者:吴春霞[1,2] 张秋萍 许红睿[1,2] 王春民 WU Chun-Xia;ZHANG Qiu-Ping;XU Hong-Rui;WANG Chun-Min(Suzhou Centers for Disease Control and prevention,Suzhou 215004,China;Jiangsu key laboratory of Food Safety Risk Monitoring(Illegal Addition Field)Suzhou 215004,China)
机构地区:[1]苏州市疾病预防控制中心,苏州215004 [2]江苏省食品安全风险监测重点实验室(非法添加领域),苏州215004
出 处:《食品安全质量检测学报》2020年第3期909-914,共6页Journal of Food Safety and Quality
基 金:苏州市科技局项目(SYS201779).
摘 要:目的建立QuEChERS-超高效液相色谱-串联三重四极杆质谱法测定蔬菜中吡虫啉、啶虫脒、氯虫苯甲酰胺和茚虫威残留的分析方法。方法样品用乙腈提取,提取液经N-丙基乙二胺(primary secondary amine,PSA)、石墨化炭黑(graphitized carbon black,GCB)混合分散剂净化,采用电喷雾正离子扫描,多反应监测模式,外标法定量。结果吡虫啉、啶虫脒、氯虫苯甲酰胺和茚虫威在5~200μg/L范围内与峰面积具有良好的线性关系,相关系数都在0.995以上,4种杀虫剂在0.5、5.0、10.0μg/kg 3个水平加标下,回收率在89.2%~101.3%范围内,相对标准偏差(relative standard deviation,RSD)在2.58%~4.85%。方法的检出限为0.003-0.054μg/kg,定量限为0.01~0.18μg/kg。结论该方法具有操作简单,迅速,准确度和灵敏度高等特点,满足测定蔬菜中4种杀虫剂残留的检测要求。Objective To establish a method for determination of 4 types of pesticide residues in vegetables by QuEChERS and ultra performance liquid chromatography tandem mass spectrometry(UPLC-MS/MS).Methods Samples were extracted by acetonitrile and purified by PSA(primary secondary amine)and GCB(graphitized carbon black,GCB),determined by UPLC-MS/MS,with positive electrospray ionization(ESI^+)in multiple reaction monitoring(MRM)mode,and quantified by external standard method.Results All pesticides showed good linearity in the concentration range of 5-200μg/L(imidacloprid,acetamiprid,chlorantraniliprole and indoxacarb)with correlation coefficient above 0.995.The recovery rates of 4 types of pesticide were between 89.2%-101.3%,and the relative standard deviations(RSDs)were between 2.58%-4.85%.The limits of detection of the method were 0.003-0.054μg/kg,and the limits of quantification were 0.01-0.018μg/kg.Conclusion This method is simple,rapid,sensitive and accurate,which is suitable for determination of 4 types of pesticide residues in vegetables.
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