Simultaneous rapid determination of 18 quinolones residues in raw milk by liquid-liquid extraction and ultra performance liquid chromatography tandem mass spectrometry
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(1. Changsha Environmental Protection College, Changsha, Hunan 410111, China; 2. Hunan Provincial Food Quality Supervision and Inspection Institute, Hunan Provincial Key Laboratory of Food Safety Monitoring and Early Warning, Changsha, Hunan 410111, China;3. Hunan Institute for Pharmaceutical Inspection, Changsha, Hunan 410001, China)

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    Abstract:

    Objective: A rapid method for simultaneous determination of 18 quinolones residues in raw milk was established. Methods: The raw milk was pretreated by liquid-liquid extraction, and the residues of 18 quinolones in raw milk were analyzed by ultra-performance liquid chromatography-tandem mass spectrometry. Results: The linearity of all the 18 quinolones from 2.0 to 100.0 ng/mL had correlation coefficients greater than 0.992. The limits of detection (LOD) of this method ranged from 0.02 to 0.50 μg/kg, and the limits of quantification (LOQ) were 0.06 to 1.50 μg/kg. The average recoveries of the 18 quinolones were 74.0% to 106.5%, with the relative standard deviation (n=6) of 1.1%~13.0%. Conclusion: The method is simple, efficient and accurate, and can be used for the quantitative confirmation of quinolones residues in raw milk.

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周艳华,李涛,潘小红,等.液液萃取—超高效液相色谱—串联质谱法快速检测原料乳中18种喹诺酮药物残留[J].食品与机械英文版,2021,37(8):63-69.

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History
  • Received:March 07,2021
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  • Online: February 15,2023
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