食品科学 ›› 2017, Vol. 38 ›› Issue (20): 197-202.doi: 10.7506/spkx1002-6630-201720028

• 安全检测 • 上一篇    下一篇

分散固相萃取-液相色谱-串联质谱法测定典型小宗作物中6 种农药残留

赵风年,郑鹭飞,佘永新,张超,洪思慧,李辉,曹晓林,王珊珊,金茂俊,金芬,邵华,王静   

  1. (中国农业科学院农业质量标准与检测技术研究所,农业部农产品质量安全重点实验室,北京 100081)
  • 出版日期:2017-10-25 发布日期:2017-09-29
  • 基金资助:
    国家自然科学基金面上项目(31471654);“十二五”国家科技支撑计划项目(2014BAD13B05-05); 中央级公益性科研院所基本科研业务费专项(1610072006009)

Determination of Six Pesticide Residues in Classic Minor Crops by Liquid Chromatography-Tandem Mass Spectrometry with Dispersive Solid Phase Extraction

ZHAO Fengnian, ZHENG Lufei, SHE Yongxin, ZHANG Chao, HONG Sihui, LI Hui, CAO Xiaolin, WANG Shanshan, JIN Maojun, JIN Fen, SHAO Hua, WANG Jing   

  1. (Key Laboratory for Agro-product Quality and Safety, Ministry of Agriculture, Institute of Quality Standard and Testing Technology for Agro-Products, Chinese Academy of Agricultural Sciences, Beijing 100081, China)
  • Online:2017-10-25 Published:2017-09-29

摘要: 建立生姜、红薯、土豆、荔枝中多菌灵、吡虫啉、涕灭威、三唑酮、乙草胺、苯醚甲环唑的液相色谱-串联质谱检测方法。样品经乙腈溶液提取,50?mg N-丙基乙二胺吸附剂、25?mg十八烷基键合硅胶(C18)净化,C18色谱柱分离,0.1%甲酸溶液-甲醇作为流动相进行梯度洗脱,在电喷雾正离子电离模式下,质谱多离子监测模式定量分析,基质标准曲线外标法定量。结果表明,6?种农药在10~500?μg/L范围内呈良好的线性关系,相关系数(r)均大于0.995。3?个加标水平下,6?种农药的平均回收率为87.9%~110.3%,相对标准偏差不大于14.6%。该方法简单、快速、灵敏度高,能够满足小宗作物农药残留的监控要求。

关键词: 小宗作物, 液相色谱-串联质谱, 农药残留, 分散固相萃取

Abstract: A simple analytical method was established using dispersive solid phase extraction combined with liquid chromatography-positive mode electrospray ionization-tandem mass spectrometric (LC-MS/MS) for the determination of six pesticide residues in ginger, sweet potato, potato, and litchi, including carbendazim, imidacloprid, aldicarb, triadimefon, acetochlor and difenoconazole. The analytes were extracted with acetonitrile and cleaned up using primary secondary amine (PSA) and octadecyl silane (C18). Qualitative analysis of six analytes was carried out under the positive scanning model after the chromatographic separation on a reversed phase C18 column with gradient elution using a mobile phase composed of methanol and 0.1% formic acid aqueous solution. A good linearity was observed for the six pesticides in the range of 10–500 μg/L with a coefficient of determination (r) of greater than 0.995. The recoveries of the pesticides in four classical minor crops were in the range of 87.9%–110.3% at three spiked concentration levels, and the precision, as indicated by relative standard deviations (RSDs, n=5), was not more than 14.6%. The method is simple, rapid and sensitive, and can meet the requirements for the determination of pesticide residues in minor crops.

Key words: minor crops, liquid chromatography-tandem mass spectrometry (LC-MS/MS), pesticide residues, dispersive solid phase extraction

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