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中國精品科技期刊2020
劉華文,鄧美晴,陳北燕. QuEChERS-超高效液相色譜-串聯質譜法測定茶葉中47種農藥殘留[J]. 食品工業科技,2024,45(9):255?264. doi: 10.13386/j.issn1002-0306.2023050213.
引用本文: 劉華文,鄧美晴,陳北燕. QuEChERS-超高效液相色譜-串聯質譜法測定茶葉中47種農藥殘留[J]. 食品工業科技,2024,45(9):255?264. doi: 10.13386/j.issn1002-0306.2023050213.
LIU Huawen, DENG Meiqing, CHEN Beiyan. Determination of 47 Pesticide Residues in Tea by QuEChERS Method Combined with Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry[J]. Science and Technology of Food Industry, 2024, 45(9): 255?264. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023050213.
Citation: LIU Huawen, DENG Meiqing, CHEN Beiyan. Determination of 47 Pesticide Residues in Tea by QuEChERS Method Combined with Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry[J]. Science and Technology of Food Industry, 2024, 45(9): 255?264. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023050213.

QuEChERS-超高效液相色譜-串聯質譜法測定茶葉中47種農藥殘留

Determination of 47 Pesticide Residues in Tea by QuEChERS Method Combined with Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry

  • 摘要: 建立一種QuEChERS-超高效液相色譜-串聯質譜法同時測定茶葉中47種農藥殘留的分析方法。樣品經1%乙酸乙腈提取,QuEChERS方法凈化,配有電噴霧離子源(ESI±)的超高效液相色譜-串聯質譜(UPLC-MS/MS),在正負離子多反應監測(MRM)模式下同時測定,基質匹配外標法定量。結果表明:47種目標化合物在一定范圍內線性關系良好,相關系數(r)為0.9971~0.9996,檢出限為0.001~0.006 mg/kg,定量限為0.002~0.020 mg/kg,平均回收率為73.4%~114.3%,相對標準偏差(n=6)為0.3%~19.9%。該方法靈敏、準確、穩定,可滿足茶葉中47種農藥殘留的檢測要求。

     

    Abstract: An analysis method for simultaneous determination of 47 kinds of pesticide residues in tea was established by QuEChERS method combined with ultra performance liquid chromatography-tandem mass spectrometry. The samples were extracted by acetonitrile containing 1% acetic acid, and purified by QuEChERS method. The 47 pesticides were determined by ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) with an electrospray ion source (ESI±) in positive and negative ion switching multiple reaction monitoring (MRM), and quantified by matrix-matched external standard method. Method validation revealed satisfactory linearities with correlation coefficients (r) between 0.9971 and 0.9996, and limits of detection were 0.001~0.006 mg/kg while the limits of quantitation were 0.002~0.020 mg/kg, the average recoveries at three spiked levels were in the range of 73.4%~114.3%, with relative standard deviations (n=6) of 0.3%~19.9%. The method is sensitive, accurate, stable, and can meet the requirements for determination of 47 pesticide residues in tea.

     

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