Stellpflug Samuel J, Kealey Samantha E, Hegarty Cullen B, Janis Gregory C
Clinical Toxicology Service and Department of Emergency Medicine, Regions Hospital, St. Paul, MN, USA,
J Med Toxicol. 2014 Mar;10(1):45-50. doi: 10.1007/s13181-013-0314-y.
2C designer drugs have been in use since the 1970s, but new drugs continue to develop from substitutions to the base phenethylamine structure. This creates new clinical profiles and difficulty with laboratory confirmation. 2-(4-Iodo-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl)methyl]ethanamine (25I-NBOMe) is a relatively new 2C drug that is more potent than structural 2C analogs; exposure reports are rare. Testing for 2C drugs is developing; specific testing for new analogs such as 25I-NBOMe is a challenge. These drugs do not reliably trigger a positive result on rapid drug immunoassays. Additionally, most facilities with confirmatory testing capabilities will not identify 25I-NBOMe; methods for detecting 25I-NBOMe in biological samples have not been clearly described nor have optimal metabolic targets for detecting 25I-NBOMe ingestion.
An 18-year-old female presented following use of 25I-NBOMe. She had an isolated brief seizure, tachycardia, hypertension, agitation, and confusion. She improved with intravenously administered fluids and benzodiazepines and was discharged 7 h postingestion. Urine was analyzed using quantitative LC-MS/MS methodology for 25I-NBOMe, 2-(4-chloro-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl)-methyl]ethanamine (25C-NBOMe), and 2-(2,5-dimethoxyphenyl)-N-(2-methoxybenzyl)ethanamine (25H-NBOMe). 25I-NBOMe was found at a concentration of 7.5 ng/mL, and 25H-NBOMe was detected as well. Additional testing was pursued to characterize the metabolism of 25I-NBOMe; the sample was reanalyzed with UPLC-time-of-flight mass spectrometry to identify excreted metabolites. The sample was additionally analyzed for the presence of 2,5-dimethoxy-4-iodophenethylamine (2C-I), 4-bromo-2,5-dimethoxyphenethylamine (2C-B), and 1-(2,5-dimethoxy-4-ethylphenyl)-2-aminoethane (2C-E).
This is a report of a patient presenting following exposure to 25I-NBOMe, a dangerous member of the evolving 2C drug class. The exposure was confirmed in a unique manner that could prove helpful in guiding further patient analysis and laboratory studies.
2C类设计药物自20世纪70年代起就已被使用,但从对苯乙胺基本结构进行取代而不断研发出新的药物。这产生了新的临床特征,也给实验室确认带来困难。2-(4-碘-2,5-二甲氧基苯基)-N-[(2-甲氧基苯基)甲基]乙胺(25I-NBOMe)是一种相对较新的2C类药物,比2C结构类似物的药效更强;关于其暴露的报告较为罕见。针对2C类药物的检测正在发展;对25I-NBOMe等新类似物进行特异性检测是一项挑战。这些药物在快速药物免疫分析中不能可靠地引发阳性结果。此外,大多数具备确证检测能力的机构无法识别25I-NBOMe;尚未明确描述生物样本中检测25I-NBOMe的方法,也未明确检测25I-NBOMe摄入的最佳代谢靶点。
一名18岁女性在使用25I-NBOMe后前来就诊。她出现了一次孤立的短暂癫痫发作、心动过速、高血压、躁动和意识模糊。经静脉补液和使用苯二氮䓬类药物后病情好转,并在摄入药物7小时后出院。使用定量液相色谱-串联质谱法对尿液进行分析,检测其中的25I-NBOMe、2-(4-氯-2,5-二甲氧基苯基)-N-[(2-甲氧基苯基)甲基]乙胺(25C-NBOMe)和2-(2,5-二甲氧基苯基)-N-(2-甲氧基苄基)乙胺(25H-NBOMe)。检测到25I-NBOMe的浓度为7.5纳克/毫升,同时也检测到了25H-NBOMe。进一步进行检测以确定25I-NBOMe的代谢特征;使用超高效液相色谱-飞行时间质谱法对样本重新分析,以识别排泄的代谢物。还对样本中2,5-二甲氧基-4-碘苯乙胺(2C-I)、4-溴-2,5-二甲氧基苯乙胺(2C-B)以及1-(2,5-二甲氧基-4-乙基苯基)-2-氨基乙烷(2C-E)的存在情况进行了分析。
本文报告了一名接触25I-NBOMe(不断演变的2C类药物中的危险成员)后的患者。以独特方式确认了此次暴露,这可能有助于指导进一步的患者分析和实验室研究。