Valen Anja, Leere Øiestad Åse Marit, Strand Dag Helge, Skari Ragnhild, Berg Thomas
Norwegian Institute of Public Health, Drug Abuse Research, Lovisenberggata 6, Oslo, 0456, Norway.
Drug Test Anal. 2017 May;9(5):808-823. doi: 10.1002/dta.2045. Epub 2016 Aug 19.
Collection of oral fluid (OF) is easy and non-invasive compared to the collection of urine and blood, and interest in OF for drug screening and diagnostic purposes is increasing. A high-throughput ultra-high-performance liquid chromatography-tandem mass spectrometry method for determination of 21 drugs in OF using fully automated 96-well plate supported liquid extraction for sample preparation is presented. The method contains a selection of classic drugs of abuse, including amphetamines, cocaine, cannabis, opioids, and benzodiazepines. The method was fully validated for 200 μL OF/buffer mix using an Intercept OF sampling kit; validation included linearity, sensitivity, precision, accuracy, extraction recovery, matrix effects, stability, and carry-over. Inter-assay precision (RSD) and accuracy (relative error) were <15% and 13 to 5%, respectively, for all compounds at concentrations equal to or higher than the lower limit of quantification. Extraction recoveries were between 58 and 76% (RSD < 8%), except for tetrahydrocannabinol and three 7-amino benzodiazepine metabolites with recoveries between 23 and 33% (RSD between 51 and 52 % and 11 and 25%, respectively). Ion enhancement or ion suppression effects were observed for a few compounds; however, to a large degree they were compensated for by the internal standards used. Deuterium-labelled and C-labelled internal standards were used for 8 and 11 of the compounds, respectively. In a comparison between Intercept and Quantisal OF kits, better recoveries and fewer matrix effects were observed for some compounds using Quantisal. The method is sensitive and robust for its purposes and has been used successfully since February 2015 for analysis of Intercept OF samples from 2600 cases in a 12-month period. Copyright © 2016 John Wiley & Sons, Ltd.
与尿液和血液采集相比,口腔液(OF)采集简便且无创,并且人们对将口腔液用于药物筛查和诊断目的的兴趣与日俱增。本文介绍了一种高通量超高效液相色谱 - 串联质谱法,该方法采用全自动96孔板支撑液液萃取进行样品前处理,用于测定口腔液中的21种药物。该方法涵盖了一系列经典的滥用药物,包括苯丙胺类、可卡因、大麻、阿片类药物和苯二氮䓬类。该方法使用Intercept OF采样试剂盒对200 μL口腔液/缓冲液混合物进行了全面验证;验证内容包括线性、灵敏度、精密度、准确度、提取回收率、基质效应、稳定性和残留。对于浓度等于或高于定量下限的所有化合物,批间精密度(RSD)和准确度(相对误差)分别<15%和13%至5%。提取回收率在58%至76%之间(RSD < 8%),但四氢大麻酚和三种7 - 氨基苯二氮䓬代谢物除外,其回收率在23%至33%之间(RSD分别在51%至52%和11%至25%之间)。观察到少数化合物存在离子增强或离子抑制效应;然而,在很大程度上它们被所使用的内标所补偿。分别对8种和11种化合物使用了氘代和碳标记的内标。在Intercept和Quantisal OF试剂盒的比较中,使用Quantisal时观察到某些化合物具有更好的回收率和更少的基质效应。该方法对于其应用目的而言灵敏且稳健,自2015年2月以来已成功用于分析12个月内2600例案件的Intercept OF样本。版权所有© 2016 John Wiley & Sons, Ltd.