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顶空-固相微萃取和衍生化后,采用气相色谱-质谱联用技术对全血中的芬氟拉明、苯丙胺和甲基苯丙胺进行简单同步分析。

Simple and simultaneous analysis of fenfluramine, amphetamine and methamphetamine in whole blood by gas chromatography-mass spectrometry after headspace-solid phase microextraction and derivatization.

作者信息

Namera A, Yashiki M, Liu J, Okajima K, Hara K, Imamura T, Kojima T

机构信息

Department of Legal Medicine, Hiroshima University School of Medicine, 1-2-3 Kasumi, Minami-ku, Hiroshima, Japan.

出版信息

Forensic Sci Int. 2000 Apr 10;109(3):215-23. doi: 10.1016/s0379-0738(00)00145-6.

Abstract

A simple and sensitive method for the simultaneous analysis of fenfluramine, amphetamine and methamphetamine in whole blood was developed using a headspace-solid phase microextraction (SPME) and derivatization. A 0.5 g whole blood sample, 5 microl d(5)-methamphetamine (50 micrig/ml) as an internal standard, and 0.5 ml sodium hydroxide (1 M) were placed into a 12 ml vial, and sealed rapidly with a silicone septum and an aluminum cap. Immediately after the vial was heated to 70 degrees C in an aluminium block heater, the needle of the SPME device was inserted through the septum of the vial, and the extraction fiber was exposed in the headspace for 15 min. First, heptafluorobutyric anhydride was injected into the injection port of the GC-MS, and the compounds extracted by the fiber were then desorbed and derivatized simultaneously by exposing the fiber in the injection port. The calibration curves, using an internal standard method, demonstrated good linearity throughout the concentration range from 0.01 to 1.0 microg/g. The detection limits of this method were 5.0 ng/g for fenfluramine and methamphetamine, and 10 ng/g for amphetamine. No interferences were found, and the time for analysis was about 30 min for one sample. This method was applied to a suicide case in which the victim ingested fenfluramine. Fenfluramine was detected in the blood sample collected from the victim at the concentration of 7.7 microg/g.

摘要

建立了一种采用顶空-固相微萃取(SPME)和衍生化技术同时分析全血中芬氟拉明、苯丙胺和甲基苯丙胺的简单灵敏方法。将0.5 g全血样品、5 μl d(5)-甲基苯丙胺(50 μg/ml)作为内标以及0.5 ml氢氧化钠(1 M)置于一个12 ml小瓶中,并用硅橡胶隔垫和铝盖迅速密封。小瓶在铝块加热器中加热至70℃后,立即将SPME装置的针头穿过小瓶的隔垫,使萃取纤维在顶空中暴露15分钟。首先,将七氟丁酸酐注入气相色谱-质谱联用仪的进样口,然后通过将纤维暴露在进样口中,使纤维萃取的化合物同时解吸和衍生化。采用内标法绘制的校准曲线在0.01至1.0 μg/g的浓度范围内显示出良好的线性。该方法对芬氟拉明和甲基苯丙胺的检测限为5.0 ng/g,对苯丙胺的检测限为10 ng/g。未发现干扰,一个样品的分析时间约为30分钟。该方法应用于一起受害者摄入芬氟拉明的自杀案件,在从受害者采集的血样中检测到芬氟拉明,浓度为7.7 μg/g。

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