Simultaneous determination of the four key fluoroquinolones and two antipsychotics in fish and shrimp by LC-MS/MS

Keyi Shen, Xiaoshuang Zou, Jun Wang
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引用次数: 4

Abstract

Abstract In this study, we developed and validated a liquid chromatography triple quadrupole tandem mass spectrometry (LC-MS/MS) method used to simultaneously determine levels of four fluoroquinolones (ofloxacin, norfloxacin, lomefloxacin, and pefloxacin) and two antipsychotics (diazepam and methaqualone) in fish and shrimp. The samples were extracted with a mixture of anhydrous sodium sulfate and acetonitrile, and purified by C18 cartridge solid-phase extraction with an optimized eluent. The MS2 method was applied to recognize the molecular structure of these compounds according to a main fragmentation scheme. The key ions of identification and quantification were deduced from chemical structures. Multiple reaction monitoring was used to quantitatively analyse the compounds of interest. Satisfactory linearities were obtained (R 2 ≥0.99) with the limits of quantitation (LOQs) ranging between 0.03 and 1.96 μg kg−1. The recoveries were 74–122%, with a relative standard deviation (RSD) below 4.9% for these compounds at the spiking level of three, five, and ten times the LODs, respectively. The LC-MS/MS method allows precise and sensitive determination of residues of six important banned veterinary drugs in fish and shrimp tissue. This methodological approach solved the problem imposed by the need for two or more analysis methods to analyse the compounds of interest described in this study.
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LC-MS/MS同时测定鱼虾中4种关键氟喹诺酮类药物和2种抗精神病药物
摘要:本研究建立了液相色谱三重四极杆串联质谱(LC-MS/MS)方法,用于同时测定鱼虾中氟喹诺酮类药物(氧氟沙星、诺氟沙星、洛美沙星和培氟沙星)和抗精神病药物(安定和甲喹酮)的含量。样品用无水硫酸钠和乙腈混合萃取,用C18筒固相萃取优化洗脱液纯化。采用MS2方法对这些化合物的分子结构进行了识别,并建立了主要的碎片化方案。从化学结构推导出鉴定和定量的关键离子。采用多反应监测法对感兴趣的化合物进行定量分析。线性关系良好(r2≥0.99),定量限(loq)范围为0.03 ~ 1.96 μg kg−1。加样回收率为74 ~ 122%,相对标准偏差(RSD)均小于4.9%,加样回收率分别为lod的3倍、5倍和10倍。LC-MS/MS方法可以精确、灵敏地测定鱼虾组织中6种重要禁用兽药的残留。这种方法解决了需要两种或更多的分析方法来分析本研究中描述的感兴趣的化合物所带来的问题。
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