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采用液相色谱-串联质谱法同时测定鱼虾中四种关键氟喹诺酮类药物和两种抗精神病药物。

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

作者信息

Shen Keyi, Zou Xiaoshuang, Wang Jun

机构信息

College of Food Science & Nutritional Engineering, China Agricultural University, Beijing, China.

出版信息

Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2022 Apr;39(4):678-686. doi: 10.1080/19440049.2022.2032381. Epub 2022 Mar 18.

DOI:10.1080/19440049.2022.2032381
PMID:35302928
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 C cartridge solid-phase extraction with an optimized eluent. The MS 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 ( ≥0.99) with the limits of quantitation (LOQs) ranging between 0.03 and 1.96 μg kg. 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.

摘要

在本研究中,我们开发并验证了一种液相色谱三重四极杆串联质谱(LC-MS/MS)方法,用于同时测定鱼和虾中四种氟喹诺酮类药物(氧氟沙星、诺氟沙星、洛美沙星和培氟沙星)以及两种抗精神病药物(地西泮和甲喹酮)的含量。样品用无水硫酸钠和乙腈的混合物进行萃取,并用优化洗脱液的C柱固相萃取法进行纯化。采用质谱法根据主要裂解模式识别这些化合物的分子结构。从化学结构推导出鉴定和定量的关键离子。采用多反应监测对目标化合物进行定量分析。获得了令人满意的线性关系(≥0.99),定量限(LOQs)在0.03至1.96μg/kg之间。在分别为检测限的3倍、5倍和10倍的加标水平下,这些化合物的回收率为74-122%,相对标准偏差(RSD)低于4.9%。LC-MS/MS方法能够精确、灵敏地测定鱼和虾组织中六种重要违禁兽药的残留量。这种方法解决了分析本研究中所述目标化合物需要两种或更多分析方法所带来的问题。

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