李俊, 蔡滔, 杜楠, 周雪丽, 王震, 袁旭, 卢平, 陈玉玲. QuEChERS-气相色谱-串联质谱法测定茶青中28种农药残留[J]. 农药学学报, 2017, 19(3): 366-373. DOI: 10.16801/j.issn.1008-7303.2017.0047
    引用本文: 李俊, 蔡滔, 杜楠, 周雪丽, 王震, 袁旭, 卢平, 陈玉玲. QuEChERS-气相色谱-串联质谱法测定茶青中28种农药残留[J]. 农药学学报, 2017, 19(3): 366-373. DOI: 10.16801/j.issn.1008-7303.2017.0047
    LI Jun, CAI Tao, DU Nan, ZHOU Xueli, WANG Zhen, YUAN Xu, LU Ping, CHEN Yuling. Determination of 28 pesticide residues in fresh tea leaves using QuEChERS-gas chromatography-tandem mass spectrometry[J]. Chinese Journal of Pesticide Science, 2017, 19(3): 366-373. DOI: 10.16801/j.issn.1008-7303.2017.0047
    Citation: LI Jun, CAI Tao, DU Nan, ZHOU Xueli, WANG Zhen, YUAN Xu, LU Ping, CHEN Yuling. Determination of 28 pesticide residues in fresh tea leaves using QuEChERS-gas chromatography-tandem mass spectrometry[J]. Chinese Journal of Pesticide Science, 2017, 19(3): 366-373. DOI: 10.16801/j.issn.1008-7303.2017.0047

    QuEChERS-气相色谱-串联质谱法测定茶青中28种农药残留

    Determination of 28 pesticide residues in fresh tea leaves using QuEChERS-gas chromatography-tandem mass spectrometry

    • 摘要: 建立了QuEChERS-气相色谱-串联质谱(GC-MS/MS)同时测定茶青中28种农药残留的分析方法。样品采用乙腈匀浆提取,经75 mg PSA、25 mg C18、4 mg GCB净化,GC-MS/MS多反应离子监测模式下检测,外标法定量。结果表明:在0.020~0.40 mg/L范围内,28种农药的质量浓度与对应的峰面积间呈良好的线性关系,决定系数均大于0.991。在0.10和0.50 mg/kg两个添加水平下,28种农药的平均回收率在77%~106%之间,相对标准偏差(RSD)在1.4%~8.0%(n=6)之间。方法的检出限(LOD)为5.0~20 μg/kg,定量限(LOQ)为10~60 μg/kg。该方法简单、快速、准确、灵敏度高,可用于茶青中多种农药残留的同时检测分析。

       

      Abstract: A multiresidue analytical method for the determination of 28 pesticide residues in fresh tea leaves was developed and evaluated by using QuEChERS (quick, easy, cheap, effective, rugged and safe) and triple-quadrupole tandem mass spectrometry (GC-MS/MS). Samples were extracted by acetonitrile, and purified by 75 mg PSA, 25 mg C18 and 4 mg GCB, followed by GC-MS/MS detection under multi-reaction monitoring (MRM) mode and quantified by external standard method. Good linearity was achieved between area size and concentration from 0.020 to 0.40 mg/L, with a coefficient of determination higher than 0.991. The average recovery at different spiking levels (0.10, 0.50 μg/kg) was ranged from 77% to 106% with RSD (relative standard deviation, n = 6) 1.4%-8.0%. The LOD (limit of detection) was 5.0-20 μg/kg, and LOQ (the limit of quantification) was 10-60 μg/kg. The method was simple, quick, accurate, highly sensitive and suitable for the simultaneous analysis of multi-residues of pesticides in fresh tea leaves.

       

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