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

IF 3.1 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Yu Zhang , John C. Halifax , Christina Tangsombatvisit , Cassandra Yun , Shaokun Pang , Shirin Hooshfar , Alan H.B. Wu , Kara L. Lynch
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引用次数: 7

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.

Abstract Image

Abstract Image

Abstract Image

高分辨率质谱法检测尿液和血清中芬太尼类似物的发展和应用
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的使用在美国呈指数级增长。由于临床实验室药物检测方法的针对性和不断变化的合成阿片类药物清单,需要替代的分析方法。方法利用美国疾病控制与预防中心(CDC)生产的芬太尼类似物筛选(FAS)试剂盒,建立液相色谱-高分辨率质谱(LC-HRMS)合成阿片类药物谱库,并采用信息依赖获取产物离子谱的数据采集方法。建立FAS试剂盒(n = 150)中合成阿片类药物在尿液和血清中的色谱保留时间、检出限和基质效应。采用FAS LC-HRMS文库分析2019年(n = 856)和2021年(n = 878)送往临床毒理学实验室进行综合药物检测的所有尿液和血清样本,回顾性(2019年)和前瞻性(2021年)确定芬太尼类似物和其他合成阿片类药物的流行情况。结果各阿片类药物在尿中的检出限为1 ~ 10 ng/mL(中值为2.5 ng/mL),在血清中的检出限为0.25 ~ 2.5 ng/mL(中值为0.5 ng/mL)。稀释和直接分析后,尿液基质效应为- 79%至86%(中位数,- 37%),蛋白质沉淀后血清基质效应为- 80%至400%(中位数,0%)。从2019年到2021年,血清样本中芬太尼/芬太尼类似物的患病率略有上升,而尿液中芬太尼/芬太尼类似物的患病率保持不变。只有2个样本被确定含有芬太尼类似物,但没有芬太尼或芬太尼代谢物的共存。对建立的MS/MS谱库进行分析,揭示了大多数芬太尼类似物的特征片段模式,可用于未来芬太尼类似物的结构解析和药物鉴定。结论LC-HRMS方法可检出综合药检常规样品中的芬太尼类似物。该方法可以进行调整,以适应不断变化的阿片类药物流行病的检测需求。
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来源期刊
Journal of Mass Spectrometry and Advances in the Clinical Lab
Journal of Mass Spectrometry and Advances in the Clinical Lab Health Professions-Medical Laboratory Technology
CiteScore
4.30
自引率
18.20%
发文量
41
审稿时长
81 days
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