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Review: LC coupled to low- and high-resolution mass spectrometry for new psychoactive substance screening in biological matrices - Where do we stand today?综述:液相色谱与低分辨率和高分辨率质谱联用用于生物基质中新精神活性物质的筛查——我们如今处于什么水平?
Anal Chim Acta. 2016 Jul 13;927:13-20. doi: 10.1016/j.aca.2016.04.046. Epub 2016 Apr 28.
3
Multiple stage MS in analysis of plasma, serum, urine and in vitro samples relevant to clinical and forensic toxicology.用于分析与临床和法医毒理学相关的血浆、血清、尿液及体外样本的多级质谱法。
Bioanalysis. 2016;8(5):457-81. doi: 10.4155/bio.16.15.
4
'Psychotropics caught in a trap' - adopting a screening approach to specific needs.“陷入困境的精神药物”——针对特定需求采用筛查方法。
Forensic Sci Int. 2014 Oct;243:84-9. doi: 10.1016/j.forsciint.2014.04.035. Epub 2014 May 6.
5
Emerging drugs of abuse.新型滥用药物。
Emerg Med Clin North Am. 2014 Feb;32(1):1-28. doi: 10.1016/j.emc.2013.09.001. Epub 2013 Oct 15.
6
Implementation of liquid chromatography/mass spectrometry into the clinical laboratory.液相色谱/质谱法在临床实验室中的应用。
Clin Chim Acta. 2013 May;420:4-10. doi: 10.1016/j.cca.2012.10.026. Epub 2012 Oct 22.
7
The utility of immunoassays for urine drug testing.免疫测定法在尿液药物检测中的应用。
Clin Lab Med. 2012 Sep;32(3):429-47. doi: 10.1016/j.cll.2012.06.004. Epub 2012 Jun 22.
8
Drugs of abuse screening in urine as part of a metabolite-based LC-MSn screening concept.尿液中滥用药物的筛选作为基于代谢物的 LC-MSn 筛选概念的一部分。
Anal Bioanal Chem. 2011 Jul;400(10):3481-9. doi: 10.1007/s00216-011-5032-1. Epub 2011 May 1.
9
Validation of analytic methods for biomarkers used in drug development.用于药物研发的生物标志物分析方法的验证。
Clin Cancer Res. 2008 Oct 1;14(19):5967-76. doi: 10.1158/1078-0432.CCR-07-4535.
10
Urine drug screening: practical guide for clinicians.尿液药物筛查:临床医生实用指南。
Mayo Clin Proc. 2008 Jan;83(1):66-76. doi: 10.4065/83.1.66.

使用布鲁克Toxtyper™检测尿液中的滥用药物:常规临床实验室环境中的经验

Detection of drugs of abuse in urine using the Bruker Toxtyper™: Experiences in a routine clinical laboratory setting.

作者信息

Ott M, Berbalk K, Plecko T, Wieland E, Shipkova M

机构信息

Zentralinstitut für Klinische Chemie und Laboratoriumsmedizin, Klinikum Stuttgart, Stuttgart, Germany.

出版信息

Clin Mass Spectrom. 2017 Aug 19;4-5:11-18. doi: 10.1016/j.clinms.2017.08.002. eCollection 2017 Apr-Aug.

DOI:10.1016/j.clinms.2017.08.002
PMID:39193128
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11322775/
Abstract

Urine screening can be used to detect misuse of illicit drugs and validate opioid replacement therapy compliance. It is common that immunochemical assays are combined with GC-MS for these applications. Bruker has recently released an ion trap mass spectrometer, called Toxtyper™, with the potential to replace current screening algorithms to detect drug misuse. Here, we compare our current strategy of urine screening for misuse of cannabis, amphetamines, cocaine, opiates, benzodiazepine, methadone, sufentanil, and pregabalin to the Toxtyper protocols provided by the manufacturer. The analytical performance of the instrument was determined on a selected drug panel and with 188 urine samples being compared to establish concordance between our currently established approach and the Toxtyper. The lower limits of detection and identification for acetylcodeine, amphetamine, benzoylecgonine, methadone, and nordiazepam were below the common cut-offs for immunological screening assays and comparable to GC-MS. Imprecision and accuracy, both within- and between-series, were consistently <25%. Toxtyper screening for pregabalin and sufentail was less sensitive than a targeted LC-MS/MS assay. Concordance met the predefined criterion of >90% for all drugs, except for pregabalin. Cannabis misuse could not be detected due to the limited sensitivity of the Toxtyper assay protocols used and the inherent imprecision of the assay. Our study has revealed that a considerable portion of our current time-consuming protocol for screening drugs of abuse in urine, based on the combination of multiple analytical methods, could be consolidated by the Toxtyper for a majority of the most-relevant substances in our patient population.

摘要

尿液筛查可用于检测非法药物的滥用情况,并验证阿片类药物替代疗法的依从性。在这些应用中,免疫化学分析与气相色谱 - 质谱联用很常见。布鲁克最近推出了一款名为Toxtyper™的离子阱质谱仪,有潜力取代当前用于检测药物滥用的筛查算法。在此,我们将目前尿液筛查大麻、苯丙胺、可卡因、阿片类药物、苯二氮卓类、美沙酮、舒芬太尼和普瑞巴林滥用情况的策略与制造商提供的Toxtyper方案进行比较。在选定的药物组上测定了该仪器的分析性能,并与188份尿液样本进行比较,以确定我们目前既定方法与Toxtyper之间的一致性。乙酰可待因、苯丙胺、苯甲酰芽子碱、美沙酮和去甲西泮的检测和鉴定下限低于免疫筛查分析的常见临界值,与气相色谱 - 质谱相当。批内和批间的不精密度和准确度始终<25%。Toxtyper对普瑞巴林和舒芬太尼的筛查比靶向液相色谱 - 串联质谱分析灵敏度低。除普瑞巴林外,所有药物的一致性均达到>90%的预定义标准。由于所用Toxtyper分析方案的灵敏度有限以及分析本身固有的不精密度,无法检测到大麻滥用情况。我们的研究表明,我们目前基于多种分析方法组合的、用于尿液中滥用药物筛查的耗时方案的很大一部分,对于我们患者群体中的大多数最相关物质,可由Toxtyper进行整合。