食品科学 ›› 2026, Vol. 47 ›› Issue (10): 368-377.doi: 10.7506/spkx1002-6630-20251125-197

• 安全检测 • 上一篇    下一篇

QuEChERS结合液相色谱-串联质谱法测定植物源性食品中9 种新型农药的残留量

陆静,白雪,梁香,朱绍华,崔凤云,成婧   

  1. (1.长沙海关技术中心,食品安全科学技术湖南省重点实验室,湖南 长沙 410004;2.中国海关科学技术研究中心,北京 100026)
  • 出版日期:2026-05-25 发布日期:2026-06-10
  • 基金资助:
    海关总署科技计划项目(2024HK114);海科中心自立课题项目(2024HX05)

Determination of Residues of Nine Novel Pesticides in Plant-Derived Foods by QuEChERS Combined with Liquid Chromatography-Tandem Mass Spectrometry

LU Jing, BAI Xue, LIANG Xiang, ZHU Shaohua, CUI Fengyun, CHENG Jing   

  1. (1. Technology Center of Changsha Customs, Hunan Key Laboratory of Food Safety Science & Technology, Changsha 410004, China; 2. Science and Technology Research Center of China Customs, Beijing 100026, China)
  • Online:2026-05-25 Published:2026-06-10

摘要: 本研究旨在建立一种利用QuEChERS(Quick、Easy、Cheap、Effective、Rugged、Safe)前处理技术结合液相色谱-串联质谱同时检测植物源性食品中9 种新型农药残留的分析方法。9 种农药包括氟噻唑菌腈、异氟苯诺喹、曼地洛宾、苯啶菌酮、苯吡噁唑烷、异环氰酰胺、吡氟丁胺、三氟咪啶酰胺和吡唑草酯。样品经体积分数1%甲酸-乙腈溶液提取,采用无水硫酸镁、氯化钠与柠檬酸钠/柠檬酸氢二钠混合盐进行盐析分层,提取液经N-丙基乙二胺、十八烷基三甲氧基硅烷和石墨化碳黑净化后,以ACQUITY UPLC HSS T3(100 mm×2.1 mm,1.8 µm)分离,以5 mmol/L乙酸铵(含体积分数0.1%甲酸)-乙腈溶液为流动相进行梯度洗脱,在多反应监测模式下进行测定,采用基质标准曲线进行定量。结果表明,9 种农药在相应质量浓度范围内线性关系良好(R2≥0.995),方法定量限为0.005~0.01 mg/kg,在0.005、0.01、0.05 mg/kg 3 个加标水平下的平均回收率为73.9%~118.1%,相对标准偏差(n=6)为0.8%~12.8%。该方法操作简便、灵敏度高、重复性好,适用于植物源性食品中多种新型农药残留的快速、准确检测。

关键词: 新型农药;植物源性食品;QuEChERS净化法;液相色谱-串联质谱

Abstract: A method for the simultaneous detection of the residues of nine novel pesticides in plant-derived foods was developed by quick, easy, cheap, effective, rugged, and safe (QuEChERS) pretreatment combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS). The pesticides included flutianil, ipflufenoquin, mandestrobin, pyriofenone, benzpyrimoxan, isocycloseram, pyflubumide, fluazaindolizine, tolpyralate. Samples were extracted with 1% formic acid in acetonitrile followed by salting-out and phase separation using anhydrous magnesium sulfate, sodium chloride and a mixture of sodium citrate and sodium dihydrogen citrate. The extracts were purified with a mixture of N-propyl-ethylenediamine (PSA), octadecyltrimethoxysilane (C18) and graphitized carbon black (GCB). The chromatographic separation was accomplished on a T3 column (100 mm × 2.1 mm, 1.8 µm) by gradient elution using a mobile phase consisting of 5 mmol/L ammonium acetate solution (containing 0.1% formic acid) and acetonitrile. The detection was carried out in the multiple reaction monitoring (MRM) mode, and the quantification was performed using a matrix-matched standard curve. The results showed that the calibration curves for all analytes exhibited a good linear relationship in the tested concentration range (R2 ≥ 0.995), the limit of quantification (LOQ) was 0.005 to 0.01 mg/kg. At three spiked levels of 0.005, 0.01 and 0.05 mg/kg, the average recoveries ranged from 73.9% to 118.1%, with relative standard deviation (RSD) ranging from 0.8% and 12.8% (n = 6). This method is rapid, accurate, sensitive, and suitable for simultaneous quantification of these novel pesticides in plant-derived foods.

Key words: novel pesticides; plant-derived foods; quick, easy, cheap, effective, rugged, and safe; liquid chromatography tandem mass spectrometry

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