Thompson W C, Dasgupta A
Department of Pathology, University of New Mexico School of Medicine, Albuquerque, USA.
Am J Clin Pathol. 1995 Aug;104(2):187-92. doi: 10.1093/ajcp/104.2.187.
The authors developed a technique by which cocaine metabolites as well as cocaethylene can be identified and quantitated using gas chromatography/mass spectrometry (GC/MS), and deuterated standards of benzoylecgonine, cocaine, ecgonine methyl ester, and cocaethylene as internal standards. The authors used a solid phase extraction (Clean Screen, Worldwide Monitoring Corporation, (Horsham, PA)) technique, and rapid derivatization of metabolites using microwave irradiation before GC/MS analysis. The t-butyldimethylsilyl derivatives (prepared by microwave irradiation in 2.5 minutes, 640 Watts [W]) offered better baseline separation and chromatography than conventional trimethylsilyl derivatives. The assay was linear between 0.87-17.3 mumol/L of benzoylecgonine (250-5,000 ng/mL) concentration, 0.83-16.6 mumol/L of cocaine (250-5,000 ng/mL), 0.79-15.8 mumol/L of cocaethylene (250-5,000 ng/mL) and 1.25-25.1 mumol/L of ecgonine methyl ester (250-5,000 ng/mL). The yields are comparable between the microwave technique and conventional heating.
作者开发了一种技术,通过该技术可使用气相色谱/质谱联用仪(GC/MS)以及作为内标的苯甲酰芽子碱、可卡因、芽子碱甲酯和可口卡因的氘代标准品来鉴定和定量可卡因代谢物以及可口卡因。作者采用了固相萃取技术(Clean Screen,全球监测公司,宾夕法尼亚州霍舍姆),并在GC/MS分析前使用微波辐射对代谢物进行快速衍生化。叔丁基二甲基甲硅烷基衍生物(通过640瓦[W]微波辐射在2.5分钟内制备)比传统的三甲基甲硅烷基衍生物具有更好的基线分离和色谱效果。该检测方法在苯甲酰芽子碱浓度为0.87 - 17.3 μmol/L(250 - 5,000 ng/mL)、可卡因为0.83 - 16.6 μmol/L(250 - 5,000 ng/mL)、可口卡因为0.79 - 15.8 μmol/L(250 - 5,000 ng/mL)以及芽子碱甲酯为1.25 - 25.1 μmol/L(250 - 5,000 ng/mL)之间呈线性关系。微波技术和传统加热的产率相当。