食品科学 ›› 2021, Vol. 42 ›› Issue (14): 308-314.doi: 10.7506/spkx1002-6630-20200622-286

• 安全检测 • 上一篇    下一篇

QuEChERS-高效液相色谱-串联质谱法测定稻田水产品中氟虫腈及其代谢物残留

马丽莎,谢文平,尹怡,单奇,刘书贵,李丽春,赵成,郑光明   

  1. (中国水产科学研究院珠江水产研究所,农业农村部水产品质量安全风险评估实验室,广东省水产动物免疫技术重点实验室,广东 广州 510380)
  • 发布日期:2021-07-27
  • 基金资助:
    国家水产品质量安全风险评估-稻渔综合种养水产品安全性评估项目(GJFP201800902); 海南省热带海洋生物技术重点实验室开放基金项目(LTMB201904)

Determination of Fipronil and Its Metabolites in Aquatic Products from Paddy Field by QuEChERS Combined with High Performance Liquid Chromatography-Tandem Mass Spectrometry

ZHANG Liyuan, ZHANG Yue, YU Runzhong, WANG Changyuan, ZHANG Dongjie   

  1. (Laboratory of Quality and Safety Risk Assessment for Aquatic Product, Minisitry of Agriculture and Rural Affairs, Key Laboratory of Aquatic Animal Immune Technology of Guangdong Province, Pear River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510380, China)
  • Published:2021-07-27

摘要: 以QuEChERS作为样品前处理方法,结合高效液相色谱-串联质谱技术建立检测稻田水产品中氟虫腈及其代谢物氟甲腈、氟虫腈砜、氟虫腈亚砜残留的方法。样品通过体积分数为0.10%甲酸-乙腈溶液及陶瓷均质子旋涡振荡法提取,由0.15 g乙二胺?N?丙基硅烷分散萃取净化后采用ZORBAX Extend-C18色谱柱(2.1 mm×100.0 mm,1.8 μm)进行分离,电喷雾负离子模式测定,基质匹配标准曲线后运用外标法定量。结果表明,稻田水产品中氟虫腈、氟甲腈、氟虫腈砜和氟虫腈亚砜的平均回收率在85.2%~112.6%之间,相对标准偏差在1.2%~12.4%之间,氟虫腈及其代谢物在质量浓度0.5~100.0 ng/mL之间线性良好,相关系数均大于0.999,检出限为1.0~1.5 μg/kg、定量限为3.0~5.0 μg/kg,二者均低于GB 2763—2019《食品中农药最大残留限量》对禽肉中氟虫腈最大残留限量10 μg/kg的规定,实验方法简单、快速、灵敏,能够满足稻田水产品中氟虫腈及其代谢物的检测需求。

关键词: 高效液相色谱-串联质谱;QuEChERS;稻田;水产品;氟虫腈及其代谢物

Abstract: A method was developed for the determination of fipronil and its metabolites including fluorocarbonitrile, fipronil sulfone and fipronil sulfide in paddy field-cultured aquatic products by quick, easy, cheap, effective, rugged and safe (QuEChERS) extraction coupled with high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Samples were extracted using acetonitrile (containing 0.10% formic acid, V/V) as the extraction solvent with vortex shaking using a ceramic homogenizer, and purified by 0.15 g of primary secondary amine (PSA) sorbent. The target compounds were separated on an Agilent ZORBAX Extend-C18 column (2.1 mm × 100.0 mm, 1.8 μm), and was detected by using an electrospray ionization (ESI) source in the negative ion mode with multiple reaction monitoring (MRM). The analytes were quantified with external standard using the matrix-matched standard calibration curve method. The results indicated that the average spiked recoveries of fipronil, fluorocarbonitrile, fipronil sulfone and fipronil sulfide in paddy field-cultured aquatic products were 85.2%–112.6% with relative standard deviations (RSDs) of 1.2%–12.4%. Good linearity was obtained in the concentration range of 0.5–100.0 ng/mL, with correlation coefficients higher than 0.999. The limit of detection (LODs) were 1.0–1.5 μg/kg, and the limit of quantitation (LOQs) were 3.0–5.0 μg/kg, which were both lower than the maximum residue limit (10 μg/kg) for fipronil in poultry meat stipulated by the national standard GB 2763–2019 Maximum Residue Limits for Pesticides in Food. The developed method was simple, sensitive and accurate, and could be used for routine analysis of fipronil and its three metabolite residues in paddy field-cultured aquatic products.

Key words: high performance liquid chromatography-tandem mass spectrometry; QuEChERS; paddy field; aquatic products; fipronil and its metabolites

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