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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development and validation of a highly sensitive gas chromatographic-mass spectrometric screening method for the simultaneous determination of nanogram levels of fentanyl, sufentanil and alfentanil in air and surface contamination wipes
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Development and validation of a highly sensitive gas chromatographic-mass spectrometric screening method for the simultaneous determination of nanogram levels of fentanyl, sufentanil and alfentanil in air and surface contamination wipes

机译:建立并验证一种同时测定空气和表面污染湿巾中芬太尼,舒芬太尼和阿芬太尼的纳克水平的高灵敏度气相色谱-质谱筛选方法

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摘要

A highly sensitive gas chromatographic-mass spectrometric (GC-MS) analytical method for the determination of the opioid narcotics fentanyl, alfentanil, and sufentanil in industrial hygiene personal air samples and surface contamination wipes was developed and comprehensively validated. Sample preparation involved a single step extraction of the samples with methanol, fortified with a fixed amount of the penta-deuterated analogues of the opioid narcotics as internal standard. The GC-MS analytical procedure using selected ion monitoring (SIM) was shown to be highly selective. Linearity was shown for levels of extracted wipe and air samples corresponding to at least 0.1-2 times their surface contamination limit (SCL) and accordingly to 0.1-2 times their time weighted average occupational exposure limit (OEL-TWA) based on a full shift 9601 air sample. Extraction recoveries were determined for spiked air samples and surface wipes and were found to be quantitative for both sampling media in the entire range studied. The air sampling method's limit of detection (LOD) was determined to be 0.4 ng per sample for fentanyl and sufentanil and 1.6 ng per sample for alfentanil, corresponding to less than 1 % of their individual OEL for a full shift air sample (9601). The limit of quantification (LOQ) was found to be 1.4, 1.2, and 5.0 ng per filter for fentanyl, sufentanil, and alfentanil, respectively. The wipe sampling method had LODs of 4 ng per wipe for fentanyl and sufentanil and 16 ng per wipe for alfentanil and LOQs of respectively, 14, 12, and 50 ng per wipe. The analytical intra-assay precision of the air sampling and wipe sampling method, defined as the coefficient of variation on the analytical result of six replicate spiked media was below 10 and 5%, respectively, for all opioids at all spike levels. Accuracy expressed as relative error was determined to be below 10%, except for alfentanil at the lowest spike level (-13.1%). The stability of the opioids during simulated air sampling was investigated. For fentanyl and sufentanil a quantitative recovery was observed at all spike levels, while for alfentanil recoveries ranged from 60.3 to 85.4%. When spiked air samples were stored at ambient temperature and at -15 degreesC quantitative recovery was found for fentanyl and sufentanil after 7 and 14 days. For alfentanil a slight loss seemed to occur upon storage during 7 days, being more explicit after 14 days. Ambient storage of spiked wipes seemed to lead to significant losses of all opioids studied, yielding recoveries of 37.7-88.3%. Upon storage of similar wipes at -15 degreesC a significantly higher recovery was found ranging from 77.3 to 88.3%. The developed analytical and sampling procedures have been recently applied in an explorative field study of which the results of surface contamination wipe sampling are presented in this paper. To our knowledge, this is the first study addressing the development and validation of analytical procedures for the assessment of external occupational exposure to potent opioid narcotics. (C) 2004 Elsevier B.V All rights reserved.
机译:开发了一种用于测定工业卫生个人空气样本和表面污染湿巾中阿片类药物芬太尼,阿芬太尼和舒芬太尼的高灵敏度气相色谱-质谱(GC-MS)分析方法,并进行了全面验证。样品制备涉及用甲醇一步萃取样品,并用固定量的阿片类药物的五氘代类似物作为内标进行强化。使用选定的离子监测(SIM)进行的GC-MS分析程序显示出高度的选择性。所显示的擦拭物和空气样品的水平显示线性,该水平对应于其表面污染极限(SCL)的至少0.1-2倍,因此其时间加权平均职业暴露极限(OEL-TWA)的0.1-2倍(基于全位移) 9601空气样本确定了加标空气样品和表面擦拭物的提取回收率,发现在整个研究范围内,两种采样介质的提取回收率都是定量的。空气采样法的检出限(LOD)被确定为芬太尼和舒芬太尼每个样品0.4 ng,阿芬太尼每个样品1.6 ng,相当于全班次空气样品的单独OEL不到1%(9601)。对于芬太尼,舒芬太尼和阿芬太尼,每个过滤器的定量限(LOQ)分别为1.4 ng,1.2 ng和5.0 ng。擦拭物抽样方法的芬太尼和舒芬太尼每擦拭物的LOD分别为4 ng,阿芬太尼和擦拭剂的LOQ分别为每擦拭物14 ng,12 ng和50 ng。空气采样和擦拭采样方法的分析内分析精度,被定义为六种重复加标介质的分析结果的变异系数分别低于10和5%(对于所有加标水平的所有阿片类药物)。测得以相对误差表示的准确度低于10%,但阿芬太尼的最低加标水平(-13.1%)除外。研究了模拟空气采样过程中阿片类药物的稳定性。对于芬太尼和舒芬太尼,在所有加标浓度下均观察到定量回收率,而对于芬太尼,回收率介于60.3%至85.4%之间。当加标的空气样品在室温和-15摄氏度下存储时,在7天和14天后发现了芬太尼和舒芬太尼的定量回收率。对于阿芬太尼,在储存7天后似乎会出现轻微损失,在14天后更为明显。尖刺抹布的环境储存似乎会导致所有所研究的阿片类药物大量流失,回收率达到37.7-88.3%。当将类似的擦巾在-15摄氏度下存储时,发现回收率明显更高,范围为77.3%至88.3%。所开发的分析和采样程序最近已在一项探索性野外研究中应用,本文介绍了表面污染擦拭采样的结果。就我们所知,这是第一项研究,其目的是分析和评估用于评估外部职业性强效阿片类药物麻醉品的分析程序。 (C)2004 Elsevier B.V保留所有权利。

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