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一种用于检测尿液和血清中芬太尼类似物的高分辨率质谱方法的开发与应用。

Development and application of a High-Resolution mass spectrometry method for the detection of fentanyl analogs in urine and serum.

作者信息

Zhang Yu, Halifax John C, Tangsombatvisit Christina, Yun Cassandra, Pang Shaokun, Hooshfar Shirin, Wu Alan H B, Lynch Kara L

机构信息

Department of Laboratory Medicine, University of California, San Francisco, and Zuckerberg San Francisco General Hospital, 1001 Potrero Ave, ZSFG Bldg. 5, 2M16 San Francisco, CA 94110, USA.

University of California, Berkeley, San Francisco, CA 94720, USA.

出版信息

J Mass Spectrom Adv Clin Lab. 2022 Jul 22;26:1-6. doi: 10.1016/j.jmsacl.2022.07.005. eCollection 2022 Nov.

Abstract

INTRODUCTION

The use of illicitly manufactured synthetic opioids, specifically fentanyl and its analogs, has escalated exponentially in the United States over the last decade. Due to the targeted nature of drug detection methods in clinical laboratories and the ever-evolving list of synthetic opioids of concern, alternative analytical approaches are needed.

METHODS

Using the fentanyl analog screening (FAS) kit produced by the Centers for Disease Control and Prevention (CDC), we developed a liquid chromatography-high resolution mass spectrometry (LC-HRMS) synthetic opioid spectral library and data acquisition method using information dependent acquisition of product ion spectra. Chromatographic retention times, limits of detection and matrix effects, in urine and serum, for the synthetic opioids in the FAS kit (n = 150) were established. All urine and serum specimens sent to a clinical toxicology laboratory for comprehensive drug testing in 2019 (n = 856) and 2021 (n = 878) were analyzed with the FAS LC-HRMS library to determine the prevalence of fentanyl analogs and other synthetic opioids, retrospectively (2019) and prospectively (2021).

RESULTS

The limit of detection (LOD) of each opioid ranged from 1 to 10 ng/mL (median, 2.5 ng/mL) in urine and 0.25-2.5 ng/mL (median, 0.5 ng/mL) in serum. Matrix effects ranged from -79 % to 86 % (median, -37 %) for urine, following dilution and direct analysis, and -80 % to 400 % (median, 0 %) for serum, following protein precipitation. The prevalence of fentanyl/fentanyl analogs in serum samples increased slightly from 2019 to 2021 while it remained the same in urine. There were only 2 samples identified that contained a fentanyl analog without the co-occurrence of fentanyl or fentanyl metabolites. Analysis of the established MS/MS spectral library revealed characteristic fragmentation patterns in most fentanyl analogs, which can be used for structure elucidation and drug identification of future analogs.

CONCLUSIONS

The LC-HRMS method was capable of detecting fentanyl analogs in routine samples sent for comprehensive drug testing. The method can be adapted to accommodate testing needs for the evolving opioid epidemic.

摘要

引言

在过去十年中,非法制造的合成阿片类药物,特别是芬太尼及其类似物在美国的使用呈指数级增长。由于临床实验室药物检测方法具有针对性,且令人担忧的合成阿片类药物清单不断变化,因此需要替代分析方法。

方法

我们使用疾病控制与预防中心(CDC)生产的芬太尼类似物筛查(FAS)试剂盒,开发了一种液相色谱 - 高分辨率质谱(LC - HRMS)合成阿片类药物光谱库和数据采集方法,该方法采用基于信息依赖的产物离子光谱采集。确定了FAS试剂盒中合成阿片类药物(n = 150)在尿液和血清中的色谱保留时间、检测限和基质效应。对2019年(n = 856)和2021年(n = 878)送往临床毒理学实验室进行全面药物检测的所有尿液和血清样本,使用FAS LC - HRMS库进行回顾性(2019年)和前瞻性(2021年)分析,以确定芬太尼类似物和其他合成阿片类药物的流行情况。

结果

每种阿片类药物在尿液中的检测限(LOD)范围为1至10 ng/mL(中位数为2.5 ng/mL),在血清中为0.25至2.5 ng/mL(中位数为0.5 ng/mL)。尿液经稀释和直接分析后,基质效应范围为 - 79%至86%(中位数为 - 37%),血清经蛋白沉淀后,基质效应范围为 - 80%至400%(中位数为0%)。血清样本中芬太尼/芬太尼类似物的流行率从2019年到2021年略有增加,而在尿液中保持不变。仅鉴定出2个样本含有芬太尼类似物,且未同时出现芬太尼或芬太尼代谢物。对已建立的MS/MS光谱库的分析揭示了大多数芬太尼类似物的特征性裂解模式,可用于未来类似物的结构解析和药物鉴定。

结论

LC - HRMS方法能够检测送往全面药物检测的常规样本中的芬太尼类似物。该方法可进行调整以适应不断演变的阿片类药物流行的检测需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a57/9440429/132b653afd31/gr1.jpg

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