Van Nimmen Nadine F J, Veulemans Hendrik A F
Laboratory for Occupational Hygiene and Toxicology, Department of Occupational, Environmental and Insurance Medicine, Katholieke Universiteit Leuven, Kapucijnenvoer 35, 6th Floor, B-3000 Leuven, Belgium.
J Chromatogr A. 2004 May 7;1035(2):249-59. doi: 10.1016/j.chroma.2004.02.074.
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 degrees C 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 degrees C 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.
开发并全面验证了一种高灵敏度气相色谱 - 质谱联用(GC - MS)分析方法,用于测定工业卫生个人空气样本和表面污染擦拭物中的阿片类麻醉剂芬太尼、阿芬太尼和舒芬太尼。样品制备包括用甲醇对样品进行单步萃取,并加入固定量的阿片类麻醉剂的五氘代类似物作为内标。使用选择离子监测(SIM)的GC - MS分析程序具有高度选择性。对于提取的擦拭物和空气样本,在至少为其表面污染限值(SCL)的0.1 - 2倍以及相应地基于全时9601空气样本为其时间加权平均职业接触限值(OEL - TWA)的0.1 - 2倍的水平下显示出线性关系。测定了加标空气样本和表面擦拭物的萃取回收率,发现在整个研究范围内两种采样介质的回收率均为定量。空气采样方法的检测限(LOD)对于芬太尼和舒芬太尼测定为每个样本0.4 ng,对于阿芬太尼为每个样本1.6 ng,对应于全时空气样本(9601)中其各自OEL的不到1%。定量限(LOQ)分别发现对于芬太尼、舒芬太尼和阿芬太尼为每个滤膜1.4、1.2和5.0 ng。擦拭采样方法对于芬太尼和舒芬太尼的LOD为每个擦拭物4 ng,对于阿芬太尼为每个擦拭物16 ng,LOQ分别为每个擦拭物14、12和50 ng。空气采样和擦拭采样方法的分析批内精密度,定义为六个重复加标介质分析结果的变异系数,对于所有阿片类药物在所有加标水平下分别低于10%和5%。以相对误差表示的准确度测定低于10%,除了最低加标水平下的阿芬太尼(-13.1%)。研究了阿片类药物在模拟空气采样过程中的稳定性。对于芬太尼和舒芬太尼,在所有加标水平下均观察到定量回收率,而对于阿芬太尼,回收率范围为60.3%至85.4%。当加标空气样本在环境温度和 - 15℃下储存时,发现芬太尼和舒芬太尼在7天和14天后定量回收。对于阿芬太尼,在储存7天期间似乎有轻微损失,14天后更明显。加标擦拭物在环境温度下储存似乎导致所研究的所有阿片类药物有显著损失,回收率为37.7% - 88.3%。当类似的擦拭物在 - 15℃下储存时,发现回收率显著更高,范围为77.3%至88.3%。最近开发的分析和采样程序已应用于一项探索性现场研究,本文展示了表面污染擦拭采样的结果。据我们所知,这是第一项针对评估强效阿片类麻醉剂外部职业暴露的分析程序的开发和验证的研究。