首页|快速滤过型净化结合超高效液相色谱-串联质谱法测定茶叶中5种农药残留量

快速滤过型净化结合超高效液相色谱-串联质谱法测定茶叶中5种农药残留量

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采用滤过型净化柱净化(m-PFC),结合超高效色谱-串联质谱仪(UPLC-MS/MS)建立了同时检测茶叶中噻螨酮、唑螨酯、炔螨特、噻嗪酮和阿维菌素等5种农药残留的方法.样品加水浸润后经乙酸乙腈均质提取,QuEChERS盐包分层,取上层提取液经m-PFC柱净化,液相色谱-质谱联用仪测定.质谱采用电喷雾正离子模式(ESI+)和多反应监测模式(MRM)进行分析,基质外标法定量.结果表明:5种农药在1.00~100.00 μg·L-1范围内线性关系良好,线性相关系数(r)均大于0.999,定量限均为5.0μg·kg-1,检出限为1.2~2.2μg·kg-1.在5.00~250.00μg·kg-1添加水平范围内,回收率为71.5%~109.9%,相对标准偏差(RSD)为2.6%~8.4%.
Determination of 5 Pesticide Residues in Tea by Multi-plug Filtration Purification Cleanup Method Combined with Ultra Performance Liquid Chromatography-tandem Mass Spectrometry
A method was established for simultaneous determination of thiamethoxam,fenpyroximate,propargite,buprofezin and abamectin residues in tea,which was based on multi-plug filtration cleanup(m-PFC)column combined with Ultra Performance Liquid Chromatography-tandem Mass Spectrome-try(UPLC-MS/MS).The samples were firstly extracted with acetic acid acetonitrile after being fully wetted with water.QuEChERS salt packs were added to the system to separate into organic and aque-ous phases,then the upper fraction was purified on a m-PFC column.The target drug residues were lastly quantified by the matrix-matched external standard method using UPLC-MS/MS in the multiple reaction monitoring(MRM)mode with positive electrospray ionization(ESI+).The results showed 5 pesticide residues had good linearity in the range of 1.00~100.00 μg·L-1 with correlation coefficient(r)above 0.999.The detection limits were in the range of 1.2~2.2 μg·kg-1,and the quantitation lim-its were 5.0 μg·kg-1.At the addition level of 5.00~250 μg·kg-1,the recoveries ranged from 71.5%to 109.9%,with relative standard deviations(RSDs)of 2.6%~8.4%(n=3).

Multi-plug filtration cleanup(m-PFC)Pesticide residuesUPLC-MS/MSTea

杜鑫、易珊珊、何家国、覃明丽、苏旭、陈绍辉、蒋金芳

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南充农产品质量监测检验中心,四川南充 637000

快速滤过型净化 农药残留 超高效液相色谱-串联质谱 茶叶

2024

云南师范大学学报(自然科学版)
云南师范大学

云南师范大学学报(自然科学版)

CSTPCD
影响因子:0.54
ISSN:1007-9793
年,卷(期):2024.44(2)
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