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Corresponding Author(s)

宫衡(1967—),男,华东理工大学教授,博士。E-mail:gongheng@ecust.edu.cn

Abstract

[Objective] To establish a new method for simultaneous detection of quinolones (QNs ) and sulfonamides (SAs) in aquatic products and livestock products.[Methods] In pretreatment,this work compares the effect of extraction solvents on the recoveries and investigates the reduction or elimination effect of purification methods such as liquid -liquid extraction (n-hexane ),dispersive adsorption of the matrix (C18 and ethylenediamine -N-propyl silylated silica ),and general solid phase extraction (PRiME HLB ) on the matrix effect.The sample is pretreated by acetonitrile with 1.0% formic acid,purified by EMR -Lipid,and separated by ACQUITY UPLC®HSST3 column (3.5 µm,2.1 mm ×100 mm ) in 10 min.MS detection is performed by multi -reaction monitoring (MRM ) in positive ion mode.QNs and SAs are quantified by the external standard method.[Results] The calibration curves of QNs and SAs exhibit a good linear relationship with the correlation coefficients (R2) exceeding 0.99,in the range of 1.0~100.0 ng/mL.The limits of detection (LODs ) and quantification (LOQs ) are 1.0 and 2.0 μg/kg,respectively.The average recoveries of QNs and SAs are between 61.9% and 115.3% under low,middle,and high spiked levels and the relative standard deviations (RSDs ) are less than 15% (n=6).[Conclusion] Compared with literature and standard methods,the established method increases the scope of application and reduces the pre -treatment process and cost.

Publication Date

4-3-2025

First Page

63

Last Page

73

DOI

10.13652/j.spjx.1003.5788.2024.80456

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