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中國精品科技期刊2020
馮麗鳳,黃芊,葉夢薇,等. QuEChERS-超高效液相色譜-串聯質譜法測定動物源性食品中30種抗寄生蟲類藥物殘留[J]. 食品工業科技,2024,45(6):280?288. doi: 10.13386/j.issn1002-0306.2023050175.
引用本文: 馮麗鳳,黃芊,葉夢薇,等. QuEChERS-超高效液相色譜-串聯質譜法測定動物源性食品中30種抗寄生蟲類藥物殘留[J]. 食品工業科技,2024,45(6):280?288. doi: 10.13386/j.issn1002-0306.2023050175.
FENG Lifeng, HUANG Qian, YE Mengwei, et al. Determination of 30 Kinds of Antiparasitic Drugs in Animal-derived Foods by QuEChERS-UPLC-MS/MS[J]. Science and Technology of Food Industry, 2024, 45(6): 280?288. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023050175.
Citation: FENG Lifeng, HUANG Qian, YE Mengwei, et al. Determination of 30 Kinds of Antiparasitic Drugs in Animal-derived Foods by QuEChERS-UPLC-MS/MS[J]. Science and Technology of Food Industry, 2024, 45(6): 280?288. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023050175.

QuEChERS-超高效液相色譜-串聯質譜法測定動物源性食品中30種抗寄生蟲類藥物殘留

Determination of 30 Kinds of Antiparasitic Drugs in Animal-derived Foods by QuEChERS-UPLC-MS/MS

  • 摘要: 目的:采用超高效液相色譜-串聯質譜法,建立測定動物源性食品中30種抗寄生蟲類藥物殘留的方法。方法:樣品經乙腈、1%氨水乙酸乙酯提取,經QuEChERS凈化。凈化后采用Waters ACQUITY UPLCTM BEH C18色譜柱分離,10 mmol/L甲酸銨(含0.1%甲酸)水溶液-乙腈:甲醇(50:50,v:v)為流動相進行梯度洗脫,電噴霧離子源正負離子切換多反應監測(Multiple Reaction Monitoring,MRM)模式下進行檢測,基質匹配外標法定量。結果:在優化的條件下,30種抗寄生蟲類藥物在各自的線性范圍內線性良好,決定系數(r2)均大于0.99;回收率為70.1%~111%;相對標準偏差在0.10%~9.1%之間(n=6);方法檢出限為0.001~0.3 μg/kg之間,方法定量限在0.004~1 μg/kg。結論:該方法靈敏、準確,具有良好的重復性和穩定性,可用于動物源性食品中多種抗寄生蟲藥物殘留的檢測。

     

    Abstract: Objective: A method for determining the residues of 30 antiparasitic drugs in animal-derived food using ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established. Methods: The samples were extracted with acetonitrile and 1% ammonia acetic ether and purified by QuEChERS. After purification, Waters ACQUITY UPLCTM BEH C18 column was used for separation, and a gradient elution of 10 mmol/L ammonium formate (containing 0.1% formic acid) aqueous solution, acetonitrile:methanol (50:50, v:v) was performed as the mobile phase. Detection was carried out using electrospray ionization (ESI) in both positive and negative ion modes using multiple reaction monitoring (MRM). Matrix-matched external standard quantification was used. Results: Under the optimized conditions, the 30 antiparasitic drugs showed good linearity within their respective linear ranges, with coefficient of determination (r2) greater than 0.99. The recoveries ranged from 70.1% to 111%, and the relative standard deviations were between 0.10% and 9.1% (n=6). The method detection limit ranged from 0.001 to 0.3 μg/kg, and the method quantification limit ranged from 0.004 to 1 μg/kg. Conclusion: The method is sensitive, accurate, and exhibits good repeatability and stability, making it suitable for detecting various antiparasitic drug residues in animal-derived food.

     

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