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Validated LC–MS-MS Method for Multiresidual Analysis of 13 Illicit Phenethylamines in Amniotic Fluid

机译:经过验证的LC-MS-MS方法可对羊水中的13种非法苯乙胺进行多残留分析

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摘要

A multi-residue analytical method was developed for the determination in amniotic fluid (AF) of 13 illicit phenethylamines, including 12 compounds never investigated in this matrix before. Samples were subject to solid-phase extraction using; hydrophilic–lipophilic balance cartridges which gave good recoveries and low matrix effects on analysis of the extracts. The quantification was performed by liquid chromatography electrospray tandem mass spectrometry. The water–acetonitrile mobile phase containing 0.1% formic acid, used with a C18 reversed phase column, provided adequate separation, resolution and signal-to-noise ratio for the analytes and the internal standard. The final optimized method was validated according to international guidelines. A monitoring campaign to assess fetal exposure to these 13 substances of abuse has been performed on AF test samples obtained from pregnant women. All mothers (n = 194) reported no use of drugs of abuse during pregnancy, and this was confirmed by the analytical data.
机译:开发了一种多残留分析方法,用于测定羊水(AF)中的13种非法苯乙胺,包括以前从未在此基质中研究过的12种化合物。样品采用以下方法进行固相萃取:亲水亲脂平衡盒,对提取物的分析具有良好的回收率和低基质效应。通过液相色谱电喷雾串联质谱法进行定量。含0.1%甲酸的水-乙腈流动相与C18反相柱一起使用,可为分析物和内标物提供足够的分离度,分离度和信噪比。最终的优化方法已根据国际准则进行了验证。已经对从孕妇获得的房颤测试样本进行了一项监测运动,以评估胎儿对这13种滥用物质的暴露程度。所有母亲(n = 194)报告称在怀孕期间未使用过滥用药物,分析数据证实了这一点。

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