食品科学 ›› 2021, Vol. 42 ›› Issue (2): 325-332.doi: 10.7506/spkx1002-6630-20200103-026

• 安全检测 • 上一篇    

QuEChERS-超高效液相色谱-串联质谱法检测禽源性食品中氟虫腈及其代谢物

戴尽波,沈洁,何啸峰,聂荣荣,董文静,梁沁娴   

  1. (梅州市食品药品监督检验所,广东 梅州 514071)
  • 出版日期:2021-01-18 发布日期:2021-01-27
  • 基金资助:
    梅州市社会发展科技计划项目(181229172051586)

Optimized QuEChERS Combined with UPLC-MS/MS for Determination of Fipronil and Its Metabolites in Poultry-Derived Foods

DAI Jinbo, SHEN Jie, HE Xiaofeng, NIE Rongrong, DONG Wenjing, LIANG Qinxian   

  1. (Meizhou Institutes for Food and Drug Control, Meizhou 514071, China)
  • Online:2021-01-18 Published:2021-01-27

摘要: 建立QuEChERS-超高效液相色谱-串联质谱检测禽源性食品中氟虫腈及其代谢物的方法。采用Plackett-Burman试验和Box-Behnken试验筛选和优化QuEChERS前处理方法中的显著影响因素。最终优化条件:样品用乙腈超声提取,后用NaCl、无水MgSO4盐析分层,提取液再用碳十八键合锆胶(Z-Sep+)、多壁碳纳米管进行净化,净化液用超高效液相色谱-串联质谱分析测定,采用基质加标曲线进行定量测定。结果表明,在鸡蛋、鸡肉、鸡肝基质中氟虫腈、氟甲腈、氟虫腈砜、氟虫腈亚的平均加标回收率在78.9%~113.5%之间,相对标准偏差在2.10%~7.60%之间,检出限在0.1~0.2 μg/kg之间,定量限为0.5 μg/kg。此方法可有效降低禽源性食品中基质效应,具有高灵敏度、精密度、准确度,可用于禽类食品中氟虫腈及其代谢物残留的快速定量测定。

关键词: QuEChERS;超高效液相色谱-串联质谱;响应面试验;氟虫腈及其代谢物;禽源性食品

Abstract: A modified quick, easy, cheap, effective, rugged and safe (QuEChERS) pretreatment coupled with ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed for the determination of fipronil and its metabolites in poultry-derived foods. Plackett-Burman design and Box-Behnken design were sequentially used to select and optimize the QuEChERS parameters with a significant influence on the recovery of analytes as well as their levels. The optimum parameters were obtained as follows: samples were extracted using acetonitrile, and the extract was salted out with a mixture of anhydrous magnesium sulfate and sodium chloride, and then purified by Z-Sep+ combined with multi-walled carbon nanotube (MWCNT) before being detected by UPLC-MS/MS and quantified by matrix-matched calibration. The results indicated that the average recoveries of fipronil, fipronil desulfinyl, fipronil sulfone and fipronil sulfide from eggs, chicken meat, and chicken liver at three different spiked levels were 78.9%–113.5%, with relative standard deviations (RSDs) of 2.10%–7.60%. The limit of detection (LOD) was 0.1–0.2 μg/kg, and the limit of quantitation (LOQ) was 0.5 μg/kg for all analytes. In the developed method, the matrix effects were effectively reduced. This method was simple, sensitive and accurate and could be used for rapid and quantitative determination of fipronil and its metabolites in poultry-derived foods.

Key words: QuEChERS; ultra-high performance liquid chromatography-tandem mass spectrometry; response surface methodology; fipronil and its metabolites; poultry-derived foods

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