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Determination of Drugs of Abuse in Airborne Particles by Pressurized Liquid Extraction and Liquid Chromatography-Electrospray-Tandem Mass Spectrometry

机译:加压液相萃取-液相色谱-电喷雾-串联质谱法测定机载颗粒中的滥用药物

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This work describes the first analytical method specifically developed for the multianalyte determination of several drugs of abuse and their metabolites in air. The methodology is based on pressurized liquid extraction (PLE) of atmospheric particles collected by means of high volume sampler equipped with quartz microfiber filters and subsequent analysis of the extracts by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Up to 17 different compounds belonging to five different chemical classes (cocainics, amphetamine-like compounds, opioids, cannabinoids, and lysergic compounds) are determined by means of this methodology. Acquisition is performed in the selected reaction monitoring (SRM) mode recording two transitions per compound (except for amphetamine). Quantitation by the internal standard method is based on the use of surrogated deuterated standards. The method has been validated in terms of linearity, accuracy, repeatability and sensitivity with satisfactory results. Absolute recoveries were above 50percent for most investigated compounds. Method precision showed relative standard deviations (RSD) below 13percent for all compounds, except for cannabinoids. The method limits of determination ranged from 0.35 pg/m~(3) (for 2-oxo-3-hydroxy-LSD) to 22.55 pg/m~(3) (for 11-nor-9 carboxy THC). Finally, as a part of the method validation, the optimized procedure was applied to the analysis of ambient air samples (fine grain-size particulates, PM_(2.5)) collected at two urban background sites in Barcelona and Madrid (Spain). Results evidenced the presence of cocaine, benzoilecgonine, tetrahydrocannabinol, ecstasy, amphetamine, methamphetamine, and heroin in some or all of the samples investigated. The highest mean daily levels corresponded to cocaine (850 pg/m~(3)) followed by heroin (143 pg/m~(3)).
机译:这项工作描述了第一种专门为多种药物及其在空气中代谢产物的多分析物测定而开发的分析方法。该方法基于通过配备石英微纤维过滤器的高容量采样器收集的大气颗粒的加压液体萃取(PLE),然后通过液相色谱-串联质谱(LC-MS / MS)对萃取物进行分析。通过这种方法,可以确定属于五个不同化学类别的多达17种不同化合物(可卡因,类苯丙胺类化合物,阿片类药物,大麻素和麦角碱化合物)。采集以选定的反应监测(SRM)模式进行,记录每个化合物的两个跃迁(苯丙胺除外)。内标法定量是基于替代的氘代标准品的使用。该方法已在线性,准确性,可重复性和灵敏度方面得到验证,结果令人满意。大多数研究化合物的绝对回收率均高于50%。方法精度显示,除大麻素外,所有化合物的相对标准偏差(RSD)均低于13%。方法的测定范围从0.35 pg / m〜(3)(对于2-oxo-3-hydroxy-LSD)到22.55 pg / m〜(3)(对于11-nor-9羧基四氢大麻酚)。最后,作为方法验证的一部分,优化的过程应用于在巴塞罗那和马德里(西班牙)的两个城市背景站点收集的环境空气样本(细粒度颗粒,PM_(2.5))的分析。结果表明,在一些或所有被调查样品中,存在可卡因,苯并ilecgonine,四氢大麻酚,摇头丸,苯丙胺,甲基苯丙胺和海洛因。日平均最高水平对应于可卡因(850 pg / m〜(3)),其次是海洛因(143 pg / m〜(3))。

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