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基质固相分散和液相色谱-串联质谱法测定鱼类和贝类中的化疗药物。

Determination of chemotherapeutic agents in fish and shellfish by matrix solid-phase dispersion and liquid chromatography-tandem mass spectrometry.

机构信息

Dpto. de Química Analítica, Nutrición y Bromatología, Facultad de Química, Universidad de Santiago de Compostela, Santiago de Compostela, Spain.

出版信息

J Sep Sci. 2012 Nov;35(21):2866-74. doi: 10.1002/jssc.201200440. Epub 2012 Oct 4.

Abstract

Chemicals are widely used in aquaculture and one of the main recipients of these analytes is the aquatic environment. The aim of this work was to develop and validate a simple and sensitive method for the determination of multiclass chemotherapeutic agents in farmed fish and shellfish using matrix solid-phase dispersion and liquid chromatography-tandem mass spectrometry. Residues of azamethiphos, three avermectins, two carbamates, and two benzoylureas were extracted from samples using silica gel as clean-up adsorbent and 0.5% acetic acid in acetonitrile as elution solvent. The extraction conditions were investigated and optimized using an experimental design. Mass spectrometry detection was carried out in positive electrospray ionization mode with multiple-reaction monitoring scan (except for benzoylurea family). Matrix-matched standards were used for the drugs quantification. Good linearity (R(2) ≥ 0.996) was observed in the range of 5-500 μg kg(-1). Limits of detection were in the range of 1.5-3.7 μg kg(-1). Recoveries from salmon samples spiked with veterinary drugs were in the range 84.9-118%. Precision was satisfactory since relative standard deviations were lower than 10.6%. The method can be successfully applied for the analysis of fish and shellfish from aquaculture.

摘要

化学品在水产养殖中被广泛应用,而这些分析物的主要受体之一是水生环境。本工作旨在开发和验证一种使用基质固相分散和液相色谱-串联质谱法测定养殖鱼类和贝类中多类化疗药物的简单灵敏方法。使用硅胶作为净化吸附剂,乙腈中的 0.5%乙酸作为洗脱溶剂,从样品中提取阿扎硫磷、三种阿维菌素、两种氨基甲酸酯和两种苯甲酰脲的残留。通过实验设计研究和优化了提取条件。采用正电喷雾电离模式,多反应监测扫描进行质谱检测(苯甲酰脲家族除外)。采用基质匹配标准品进行药物定量。在所研究的浓度范围内(5-500 μg kg(-1)),均观察到良好的线性关系(R(2)≥0.996)。检测限在 1.5-3.7 μg kg(-1)范围内。在鲑鱼样品中添加兽药的回收率在 84.9-118%范围内。精密度令人满意,因为相对标准偏差低于 10.6%。该方法可成功应用于养殖鱼类和贝类的分析。

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