Poklis Justin L, Charles Jezelle, Wolf Carl E, Poklis Alphonse
Department of Pharmacology and Toxicology, Virginia Commonwealth, University, Richmond, VA, USA.
Biomed Chromatogr. 2013 Dec;27(12):1794-800. doi: 10.1002/bmc.2999. Epub 2013 Jul 25.
2CC-NBOMe {4-chloro-2,5-dimethoxyphenethyl-N-[(2-methoxyphenyl) methyl] ethanamine} and 25I-NBOMe {2-(4-iodo-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl) methyl] ethanamine} are of a class of N-benzyl phenethylamine derivatives whose synthesis was first reported in the scientific literature in 2011. Recent reports from 'personal drug experience websites' and in the popular press indicate these drugs are the latest in a series of designer 'Bath Salt' drugs of abuse. The presented high-performance liquid chromatography triple quadrupole mass spectrometry (HPLC/MS/MS) method was developed for the detection and quantification of 2CC-NBOMe and 25I-NBOMe in serum of intoxicated emergency department patients. The assay applies 2-(2,5-dimethoxyphenyl)-N-(2-methoxybenzyl) ethanamine (25H-NBOMe) as the internal standard. Samples were extracted using solid-phase extraction columns. The chromatographic separation was performed on a Luna 3 µ C8(2) 100 Å, 100 × 2.0 mm, column. Detection was accomplished by multiple-reaction monitoring via an electrospray ionization source operating in the positive ionization mode. The calibration curves were linear over the investigated concentration range, 30-2000 pg/mL, with a lower limit of detection of 10 pg/mL for both 2CC-NBOMe and 25I-NBOMe. The method proved suitable for serum clinical toxicology testing. Two severely intoxicated emergency department patients were determined to have serum concentrations of 250 and 2780 pg/mL of 25I-NBOMe using the presented method.
2C-C-NBOMe{4-氯-2,5-二甲氧基苯乙-N-[(2-甲氧基苯基)甲基]乙胺}和25I-NBOMe{2-(4-碘-2,5-二甲氧基苯基)-N-[(2-甲氧基苯基)甲基]乙胺}属于一类N-苄基苯乙胺衍生物,其合成最早于2011年在科学文献中报道。来自“个人药物体验网站”和大众媒体的最新报道表明,这些药物是一系列新型“浴盐”滥用药物中的最新品种。本文所介绍的高效液相色谱-三重四极杆质谱法(HPLC/MS/MS)是为检测和定量中毒急诊科患者血清中的2C-C-NBOMe和25I-NBOMe而开发的。该测定法使用2-(2,5-二甲氧基苯基)-N-(2-甲氧基苄基)乙胺(25H-NBOMe)作为内标。样品采用固相萃取柱进行萃取。色谱分离在Luna 3 µ C8(2) 100 Å、100×2.0 mm的色谱柱上进行。通过在正离子模式下运行的电喷雾电离源进行多反应监测来完成检测。校准曲线在所研究的浓度范围30 - 2000 pg/mL内呈线性,2C-C-NBOMe和25I-NBOMe两者的检测下限均为10 pg/mL。该方法被证明适用于血清临床毒理学检测。使用本文所介绍方法测定的两名严重中毒的急诊科患者血清中25I-NBOMe的浓度分别为250和2780 pg/mL。