Forensic Science Center, Lawrence Livermore National Laboratory, Livermore, CA, United States of America.
Nuclear and Chemical Sciences Division, Lawrence Livermore National Laboratory, Livermore, CA, United States of America.
PLoS One. 2022 Nov 2;17(11):e0275931. doi: 10.1371/journal.pone.0275931. eCollection 2022.
Electron Impact Gas Chromatography-Mass Spectrometry (EI-GC-MS) and High Resolution Liquid Chromatography-Mass Spectrometry (HR-LC-MS) have been used in the analysis of products arising from the trichloroethoxycarbonylation of fentanyl and acetylfentanyl in urine and plasma matrices. The method involves the initial extraction of both synthetic opioids separately from the matrices followed by detection of the unique products that arise from their reaction with 2,2,2-trichloroethoxycarbonyl chloride (Troc-Cl), namely Troc-norfentanyl and Troc-noracetylfentanyl. The optimized protocol was successfully evaluated for its efficacy at detecting these species formed from fentanyl and acetylfentanyl when present at low and high levels in urine (fentanyl: 5 and 10 ng/mL and acetylfentanyl: 20 and 100 ng/mL) and plasma (fentanyl: 10 and 20 ng/mL and acetylfentanyl: 50 and 200 ng/mL), values that reflect levels reported in overdose victims. The HR-LC-MS method's LOQ (limit of quantitation) for the Troc-norfentanyl and Troc-noracetylfentanyl products was determined to be ~10 ng/mL for both species. Even though the superiority in the detection of these species by HR-LC-MS over EI-GC-MS, the latter method proved to be important in the detection of the second product from the reaction, namely 2-phenylethyl chloride that is crucial in the determination of the original opioid. This observation highlights the importance of using complimentary analytical techniques in the analysis of a sample, whether biological or environmental in nature. The method herein serves as a complementary, qualitative confirmation for the presence of a fentanyl in collected urine, plasma and by extension other biological samples amenable to the common extraction procedures described for opioid analysis. More importantly, the method's main strength comes from its ability to react with unknown fentanyls to yield products that can be not only detected by EI-GC-MS and HR-LC-MS but can then be used to retrospectively identify an unknown fentanyl.
电子冲击气相色谱-质谱法(EI-GC-MS)和高分辨率液相色谱-质谱法(HR-LC-MS)已用于分析尿液和血浆基质中三氯乙氧基羰基化芬太尼和乙酰芬太尼产生的产物。该方法涉及从基质中分别提取两种合成阿片类药物,然后检测它们与 2,2,2-三氯乙氧基羰基氯(Troc-Cl)反应产生的独特产物,即 Troc-纳洛啡和 Troc-纳乙酰芬太尼。该优化方案成功评估了其在检测尿液中低水平和高水平(芬太尼:5 和 10ng/mL,乙酰芬太尼:20 和 100ng/mL)和血浆中(芬太尼:10 和 20ng/mL,乙酰芬太尼:50 和 200ng/mL)形成的这些物质的效力,这些值反映了过量受害者报告的水平。HR-LC-MS 方法对 Troc-纳洛啡和 Troc-纳乙酰芬太尼产物的 LOQ(定量限)确定为两种物质均约为 10ng/mL。尽管 HR-LC-MS 检测这些物质的优越性,但后者方法在检测反应的第二种产物,即 2-苯乙基氯方面非常重要,因为它是确定原始阿片类药物的关键。这一观察结果强调了在分析样品(无论是生物样品还是环境样品)时使用互补分析技术的重要性。本方法可作为在收集的尿液、血浆中存在芬太尼的补充定性确证,并且可扩展到其他可通过适用于阿片类分析的常见提取程序处理的生物样本。更重要的是,该方法的主要优势在于它能够与未知的芬太尼反应,产生不仅可以通过 EI-GC-MS 和 HR-LC-MS 检测,而且可以用于追溯鉴定未知芬太尼的产物。