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死后尿液中免疫分析法与超高效液相色谱/高分辨率飞行时间质谱法药物筛查的比较

Comparison between drug screening by immunoassay and ultra-high performance liquid chromatography/high-resolution time-of-flight mass spectrometry in post-mortem urine.

作者信息

Sundström Mira, Pelander Anna, Ojanperä Ilkka

机构信息

Hjelt Institute, Department of Forensic Medicine, Forensic Toxicology Division, University of Helsinki, PO Box 40, 00014, Helsinki, Finland.

出版信息

Drug Test Anal. 2015 May;7(5):420-7. doi: 10.1002/dta.1683. Epub 2014 Jun 20.

Abstract

Immunoassay is currently the most common approach for urine drug screening. However, the continuous emergence of new psychoactive substances (NPS) and their low urinary concentrations have challenged the scope and sensitivity of immunoassays. Consequently, specialized toxicology laboratories rely more and more on mass spectrometry (MS) based techniques. Ultra-high performance liquid chromatography/high-resolution time-of-flight mass spectrometry (UHPLC-HR-TOF-MS) is an especially attractive technique for comprehensive drug screening. The objective was to compare the performances of immunoassay and UHPLC-HR-TOF-MS in terms of scope, flexibility, sensitivity, and reliability of substance identification. A total of 279 post-mortem urine samples were analyzed using a method representative of each technique. The immunoassay method was an Emit II Plus enzyme immunoassay for the following drug groups: amphetamines, benzodiazepines, buprenorphine, cannabis, and opiates. The UHPLC-HR-TOF-MS method was a recently published method covering hundreds of drugs: conventional drugs of abuse, abused prescription drugs, and NPS of various classes. UHPLC-HR-TOF-MS produced a lower number of false positive (FP) results for the drug groups covered by immunoassay. Many of the false negative (FN, n = 40) and FP (n = 22) immunoassay results were obviously due to the higher cut-off concentrations and interfering matrix, respectively. Moreover, the wider scope of UHPLC-HR-TOF-MS allowed detection of NPS and prescription drugs. UHPLC-HR-TOF-MS gave FP results related to a few particular substances. The future option of adjusting all compound-specific reporting parameters individually would allow the method's sensitivity and specificity to be fully exploited.

摘要

免疫测定法是目前尿液药物筛查最常用的方法。然而,新型精神活性物质(NPS)不断出现,且它们在尿液中的浓度较低,这对免疫测定法的检测范围和灵敏度提出了挑战。因此,专业毒理学实验室越来越依赖基于质谱(MS)的技术。超高效液相色谱/高分辨率飞行时间质谱(UHPLC-HR-TOF-MS)是一种极具吸引力的全面药物筛查技术。目的是比较免疫测定法和UHPLC-HR-TOF-MS在物质鉴定的范围、灵活性、灵敏度和可靠性方面的性能。使用每种技术的代表性方法对总共279份尸检尿液样本进行了分析。免疫测定法采用Emit II Plus酶免疫测定法检测以下药物类别:苯丙胺类、苯二氮䓬类、丁丙诺啡、大麻和阿片类药物。UHPLC-HR-TOF-MS方法是最近发表的一种涵盖数百种药物的方法:传统滥用药物、滥用处方药和各类NPS。对于免疫测定法所涵盖的药物类别,UHPLC-HR-TOF-MS产生的假阳性(FP)结果数量较少。许多免疫测定法的假阴性(FN,n = 40)和FP(n = 22)结果显然分别是由于较高的截断浓度和干扰基质所致。此外,UHPLC-HR-TOF-MS更广泛的检测范围能够检测出NPS和处方药。UHPLC-HR-TOF-MS产生了与少数特定物质相关的FP结果。未来单独调整所有化合物特异性报告参数的选项将使该方法的灵敏度和特异性得到充分利用。

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