Saito Takeshi, Mase Hiroyasu, Takeichi Sanae, Inokuchi Sadaki
Department of Emergency and Critical Care Medicine, Tokai University School of Medicine, Isehara, Kanagawa 259-1193, Japan.
J Pharm Biomed Anal. 2007 Jan 4;43(1):358-63. doi: 10.1016/j.jpba.2006.06.031. Epub 2006 Jul 26.
This paper presents a simple and sensitive chromatographic procedure for the simultaneous determination and quantification of ephedrines, amphetamines, cocaine, cocaine metabolites, and opiates in human urine by gas chromatography-mass spectrometry. This method involves enzyme hydrolysis in the presence of a deuterated internal standard, liquid-liquid extraction, and derivatization with pentafluoropropionic anhydride and pentafluoropropanol. The recovery of each compound averaged at 65.8% or more. The limits of detection determined for each compound by using a 2-mL sample volume ranged from 5 to 50 ng/mL. The calibration curves were linear to 100 ng/mL for all compounds when determined using methamphetamine-d4 and MDMA-d5 as internal standards. This method was successfully applied for the analysis of urine samples suspected to contain intoxicants such as methamphetamine and heroin.
本文介绍了一种简单且灵敏的色谱方法,用于通过气相色谱 - 质谱联用同时测定和定量人尿中的麻黄碱、苯丙胺、可卡因、可卡因代谢物和阿片类物质。该方法包括在氘代内标存在下的酶水解、液 - 液萃取以及用五氟丙酸酐和五氟丙醇进行衍生化。每种化合物的回收率平均为65.8%或更高。使用2 mL样品体积测定的每种化合物的检测限为5至50 ng/mL。当使用甲基苯丙胺 - d4和摇头丸 - d5作为内标进行测定时,所有化合物的校准曲线在100 ng/mL范围内呈线性。该方法已成功应用于分析疑似含有甲基苯丙胺和海洛因等毒物的尿液样本。