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通过固相萃取和液相色谱-串联质谱法对保存的口腔液中多种非法药物进行定量分析。

Quantitative analysis of multiple illicit drugs in preserved oral fluid by solid-phase extraction and liquid chromatography-tandem mass spectrometry.

作者信息

Wood Michelle, Laloup Marleen, Ramirez Fernandez Maria del Mar, Jenkins Kevin M, Young Michael S, Ramaekers Jan G, De Boeck Gert, Samyn Nele

机构信息

Waters Corporation, MS Technologies Centre, Manchester, UK.

出版信息

Forensic Sci Int. 2005 Jun 10;150(2-3):227-38. doi: 10.1016/j.forsciint.2004.11.027. Epub 2005 Apr 18.

Abstract

We present a validated method for the simultaneous analysis of basic drugs which comprises a sample clean-up step, using mixed-mode solid-phase extraction (SPE), followed by LC-MS/MS analysis. Deuterated analogues for all of the analytes of interest were used for quantitation. The applied HPLC gradient ensured the elution of all the drugs examined within 14 min and produced chromatographic peaks of acceptable symmetry. Selectivity of the method was achieved by a combination of retention time, and two precursor-product ion transitions for the non-deuterated analogues. Oral fluid was collected with the Intercept, a FDA approved sampling device that is used on a large scale in the US for workplace drug testing. However, this collection system contains some ingredients (stabilizers and preservatives) that can cause substantial interferences, e.g. ion suppression or enhancement during LC-MS/MS analysis, in the absence of suitable sample pre-treatment. The use of the SPE was demonstrated to be highly effective and led to significant decreases in the interferences. Extraction was found to be both reproducible and efficient with recoveries >76% for all of the analytes. Furthermore, the processed samples were demonstrated to be stable for 48 h, except for cocaine and benzoylecgonine, where a slight negative trend was observed, but did not compromise the quantitation. In all cases the method was linear over the range investigated (2-200 microg/L) with an excellent intra-assay and inter-assay precision (coefficients of variation <10% in most cases) for QC samples spiked at a concentration of 4, 12 and 100 microg/L. Limits of quantitation were estimated to be at 2 microg/L with limits of detection ranging from 0.2 to 0.5 microg/L, which meets the requirements of SAMHSA for oral fluid testing in the workplace. The method was subsequently applied to the analysis of Intercept samples collected at the roadside by the police, and to determine MDMA and MDA levels in oral fluid samples from a controlled study.

摘要

我们提出了一种经过验证的同时分析碱性药物的方法,该方法包括一个样品净化步骤,即使用混合模式固相萃取(SPE),随后进行液相色谱-串联质谱(LC-MS/MS)分析。所有目标分析物的氘代类似物用于定量。所应用的高效液相色谱梯度确保了所有检测药物在14分钟内洗脱,并产生了对称性可接受的色谱峰。该方法的选择性通过保留时间以及非氘代类似物的两个前体-产物离子跃迁来实现。使用Intercept收集口腔液,Intercept是一种经美国食品药品监督管理局(FDA)批准的采样装置,在美国大规模用于工作场所药物检测。然而,在没有合适的样品预处理的情况下,这种收集系统包含一些成分(稳定剂和防腐剂),可能会导致严重干扰,例如在LC-MS/MS分析期间的离子抑制或增强。结果表明,使用SPE非常有效,可显著减少干扰。发现萃取具有可重复性且效率高,所有分析物的回收率均>76%。此外,除可卡因和苯甲酰爱康宁外,处理后的样品在48小时内稳定,尽管观察到有轻微的负趋势,但不影响定量。在所有情况下,该方法在所研究的范围内(2 - 200μg/L)呈线性,对于浓度为4、12和100μg/L加标的质量控制(QC)样品,具有出色的批内和批间精密度(大多数情况下变异系数<10%)。定量限估计为2μg/L,检测限范围为0.2至0.5μg/L,这符合美国药物滥用和精神健康服务管理局(SAMHSA)对工作场所口腔液检测的要求。该方法随后应用于分析警方在路边收集的Intercept样品,并用于确定对照研究中口腔液样品中的摇头丸(MDMA)和甲烯二氧苯丙胺(MDA)水平。

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