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中国精品科技期刊2020
冯丽凤,黄芊,叶梦薇,等. QuEChERS-超高效液相色谱-串联质谱法测定动物源性食品中30种抗寄生虫类药物残留[J]. 食品工业科技,2024,45(6):280−288. doi: 10.13386/j.issn1002-0306.2023050175.
引用本文: 冯丽凤,黄芊,叶梦薇,等. QuEChERS-超高效液相色谱-串联质谱法测定动物源性食品中30种抗寄生虫类药物残留[J]. 食品工业科技,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-超高效液相色谱-串联质谱法测定动物源性食品中30种抗寄生虫类药物残留

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

  • 摘要: 目的:采用超高效液相色谱-串联质谱法,建立测定动物源性食品中30种抗寄生虫类药物残留的方法。方法:样品经乙腈、1%氨水乙酸乙酯提取,经QuEChERS净化。净化后采用Waters ACQUITY UPLCTM BEH C18色谱柱分离,10 mmol/L甲酸铵(含0.1%甲酸)水溶液-乙腈:甲醇(50:50,v:v)为流动相进行梯度洗脱,电喷雾离子源正负离子切换多反应监测(Multiple Reaction Monitoring,MRM)模式下进行检测,基质匹配外标法定量。结果:在优化的条件下,30种抗寄生虫类药物在各自的线性范围内线性良好,决定系数(r2)均大于0.99;回收率为70.1%~111%;相对标准偏差在0.10%~9.1%之间(n=6);方法检出限为0.001~0.3 μg/kg之间,方法定量限在0.004~1 μg/kg。结论:该方法灵敏、准确,具有良好的重复性和稳定性,可用于动物源性食品中多种抗寄生虫药物残留的检测。

     

    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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