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高效液相色谱-串联质谱法测定尿液中九种致幻 25-NBOMe 设计药物

High-performance liquid chromatography with tandem mass spectrometry for the determination of nine hallucinogenic 25-NBOMe designer drugs in urine specimens.

机构信息

1Department of Pharmacology and Toxicology, Virginia Commonwealth University, PO Box 980613, Richmond, VA 23298-0613, USA.

出版信息

J Anal Toxicol. 2014 Apr;38(3):113-21. doi: 10.1093/jat/bku005. Epub 2014 Feb 16.

Abstract

We present a high-performance liquid chromatography triple quadrupole mass spectrometry (HPLC-MS-MS) method for the identification and quantification of nine serotonin 5-HT2A receptor agonist hallucinogenic substances from a new class of N-methoxybenzyl derivatives of methoxyphenylethylamine (NBOMe) designer drugs in human urine: 25H-NBOMe, 2CC-NBOMe, 25I-NBF, 25D-NBOMe, 25B-NBOMe, 2CT-NBOMe, 25I-NBMD, 25G-NBOMe and 25I-NBOMe. This assay was developed for the Virginia Commonwealth University Clinical and Forensic Toxicology laboratory to screen emergency department specimens in response to an outbreak of N-benzyl-phenethylamine derivative abuse and overdose cases in Virginia. The NBOMe derivatives were rapidly extracted from the urine specimens by use of FASt™ solid-phase extraction columns. Assay performance was determined as recommended for validation by the Scientific Working Group for Forensic Toxicology (SWGTOX) for linearity, lower limit of quantification, lower limit of detection, accuracy/bias, precision, dilution integrity, carryover, selectivity, absolute recovery, ion suppression and stability. Linearity was verified to be from 1 to 100 ng/mL for each of the nine analytes. The bias determined for the NBOMe derivatives was 86-116% with a <14% coefficient of variation over the linear range of the assay. Four different NBOMe derivatives were detected using the presented method in patient urine specimens.

摘要

我们提出了一种高效液相色谱三重四极杆质谱(HPLC-MS-MS)方法,用于鉴定和定量从新型 N-甲氧基苄基取代的苯乙胺(NBOMe)设计药物中提取的 9 种 5-羟色胺 5-HT2A 受体激动剂致幻物质在人尿中的存在:25H-NBOMe、2CC-NBOMe、25I-NBF、25D-NBOMe、25B-NBOMe、2CT-NBOMe、25I-NBMD、25G-NBOMe 和 25I-NBOMe。该检测方法是为弗吉尼亚联邦大学临床和法医毒理学实验室开发的,用于筛选急诊标本,以应对弗吉尼亚州 N-苯乙胺衍生物滥用和过量病例的爆发。NBOMe 衍生物通过使用 FASt™固相萃取柱从尿样中快速提取。根据法医毒理学科学工作组(SWGTOX)的验证建议,对 NBOMe 衍生物的分析性能进行了测定,包括线性、定量下限、检测下限、准确度/偏差、精密度、稀释完整性、交叉污染、选择性、绝对回收率、离子抑制和稳定性。每个 9 种分析物的线性范围均为 1 至 100ng/mL。NBOMe 衍生物的偏差确定为 86-116%,在测定线性范围内的变异系数小于 14%。该方法在患者尿样中检测到了 4 种不同的 NBOMe 衍生物。

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