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首页> 外文期刊>Analytical and bioanalytical chemistry >Development and validation of fast UHPLC-MS/MS screening method for 87 NPS and 32 other drugs of abuse in hair and nails: application to real cases
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Development and validation of fast UHPLC-MS/MS screening method for 87 NPS and 32 other drugs of abuse in hair and nails: application to real cases

机译:快速UHPLC-MS / MS筛选方法的开发与验证87个NPS和32种头发和指甲中其他滥用药物:实际情况应用

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Interest on keratinized matrix analysis for clinical and forensic purposes has been recently grown due to the wide temporary detection window for psychotropic and toxic substances entrapped after repeated consumption. The aim of this study was the development and full validation of an UHPLC-MS/MS screening method to quantify 119 molecules among most abused classic drugs and new psychoactive substances in hair and in nails, to assess the polyconsumption. Twenty-five milligrams of hair or nail samples, added with the internal standard mixture, were cut and incubated with 500 mu L M3 (R) buffer reagent at controlled temperature. After cooling, 1 mu L supernatant was injected in the chromatographic system equipped with an Oasis HLB column. After the 10 min chromatographic separation through a gradient mobile phase (aqueous ammonium formate, phase A; acetonitrile, phase B), the target compounds were detected in multiple reaction monitoring mode. The method was linear (r(2) always better than 0.99) in a calibration range of LOQ 20000 pg compound for milligram hair and of LOQ 1000 pg compound per milligram nail. Process efficiency of analytes under investigation was always better than 65% and no significant ion suppression due to matrix effect was observed. Intra-assay and inter-assay precision and accuracy were always better than 15%. The applicability and trueness of the method were examined by analysing real samples of hair and nail from users of psychoactive drugs in recreational contexts. Both classic drugs and new psychoactive substances could be determined as result of single or repeated use and accumulation in keratin matrices.
机译:最近由于在重复消费后捕获的精神和有毒物质的临时临时检测窗口,最近已经生长了对临床和法医目的的角化基质分析的兴趣。本研究的目的是UHPLC-MS / MS筛选方法的开发和全面验证,以量化119种毛发和指甲中的最滥用的经典药物和新的精神活性物质中的119分子。将25毫克的头发或钉子样品加入内标混合物,并在受控温度下用500μLM3(R)缓冲试剂温育。冷却后,在配备有Oasis HLB柱的色谱系统中注射1μl上清液。通过梯度流动相10分钟的色谱分离(甲酸铵水溶液,A相;乙腈,相B),在多重反应监测模式下检测目标化合物。该方法在Loq 20000 pg化合物的校准范围内为线性(R(2)始终优于0.99),用于毫克头发和每毫克钉的LOQ 1000 pg化合物。在调查下分析物的过程效率总是优于65%,并且观察到由于基质效应而没有显着的离子抑制。测定内和测定间精度和精度总是优于15%。通过在娱乐环境中分析来自精神活性药物的用户的真正的头发样本和钉子的真正样本来检查该方法的适用性和特鲁。经典药物和新的精神活性物质都可以根据单人或反复使用和角蛋白基质积累来确定。

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