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采用磁固相萃取-液相色谱串联质谱法同时测定淡水鱼样品中的 11 种喹诺酮类残留。

Simultaneous determination of 11 quinolone residues in freshwater fish samples by magnetic solid-extraction coupled to liquid chromatography-tandem mass spectrometry.

机构信息

Key Laboratory of Health Risk Appraisal for Trace Toxic Chemicals of Zhejiang Province, Ningbo Municipal Center for Disease Control and Prevention, Ningbo, Zhejiang Province, 315010, P. R. China.

Hangzhou BOSOM New Materials Technology Co., Ltd, Hangzhou, Zhejiang Province, 311103, P. R. China.

出版信息

J Sep Sci. 2021 Nov;44(21):4017-4024. doi: 10.1002/jssc.202100554. Epub 2021 Sep 4.

DOI:10.1002/jssc.202100554
PMID:34453397
Abstract

In this study, well-defined core-shell ethylenediamine-functional magnetic ferroferric oxide polymers were prepared and were fully characterized by transmission electron microscopy, scanning electron microscopy, FTIR spectroscopy, and vibrating sample magnetometry. Then, it was used as a magnetic solid-phase extraction adsorbent for simultaneous determination of 11 trace quinolone residues in freshwater fish samples coupled to liquid chromatography-tandem mass spectrometry. The obtained results revealed that the adsorbent showed good extraction efficiency and the adsorption mechanisms referred to hydrogen bond and π-π stacking interaction. Moreover, the magnetic solid-phase extraction conditions were also carefully optimized. The limits of quantitation of 11 quinolones were in the range of 0.15-0.36 μg/kg, while spiking recoveries were in the range of 80.2-99.5% for the 11 quinolones in freshwater fish samples at four spiked levels including limits of quantitation, 1.0, 40.0, and 80.0 μg/kg with the relative standard deviations ranging from 0.8 to 9.1%. The proposed method was applied to analyze 45 freshwater fish samples, and enrofloxacin was detected in 91.1% samples with concentrations ranging from 0.659 to 333 μg/kg. It could be concluded that the proposed method is fast, simple, sensitive, and accurate for the routine monitor of freshwater fish.

摘要

在这项研究中,制备了具有明确核壳结构的乙二胺功能化磁性四氧化三铁聚合物,并通过透射电子显微镜、扫描电子显微镜、傅里叶变换红外光谱和振动样品磁强计对其进行了全面表征。然后,将其用作磁固相萃取吸附剂,结合液相色谱-串联质谱法同时测定淡水鱼样品中的 11 种痕量喹诺酮残留。结果表明,该吸附剂具有良好的萃取效率,吸附机制涉及氢键和π-π堆积相互作用。此外,还对磁固相萃取条件进行了仔细优化。11 种喹诺酮的定量限范围为 0.15-0.36μg/kg,在淡水鱼样品的四个加标水平(包括定量限、1.0、40.0 和 80.0μg/kg)下,11 种喹诺酮的加标回收率范围为 80.2-99.5%,相对标准偏差范围为 0.8-9.1%。该方法应用于分析 45 个淡水鱼样品,检测到 91.1%的样品中含有恩诺沙星,浓度范围为 0.659-333μg/kg。可以得出结论,该方法快速、简单、灵敏、准确,可用于淡水鱼的常规监测。

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