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固相微萃取-气相色谱-质谱法测定人发中的可卡因和可卡乙碱

Solid-phase microextraction for the determination of cocaine and cocaethylene in human hair by gas chromatography-mass spectrometry.

作者信息

Bermejo Ana María, López Patricia, Alvarez Iván, Tabernero María Jesús, Fernández Purificación

机构信息

Institute of Legal Medicine, Forensic Toxicology Service, Faculty of Medicine, San Francisco, s/n, 15782 Santiago de Compostela, Spain.

出版信息

Forensic Sci Int. 2006 Jan 6;156(1):2-8. doi: 10.1016/j.forsciint.2005.09.007. Epub 2005 Oct 19.

Abstract

A method for the simultaneous determination of cocaine (COC) and cocaethylene (CE) in human hair was developed, using solid-phase microextraction (SPME) and gas chromatography-mass spectrometry (GC-MS) as analytical technique to identify and quantify the drugs. Selected ion monitoring (SIM) mode was used to obtain higher sensitivity. The deuterated-labeled analogues were used as internal standards. The detector response was linear for the drugs studied over the range 0.4-15 ng/mg, with correlation coefficients higher than 0.995. The coefficients of variation oscillated between 0.65% and 14.18% and the accuracy was in the range from 0.73% to 11.20%. The limits of quantitation and detection were found to be acceptable. Finally, this method was applied to 15 hair samples from cocaine users, obtaining positive results in all cases. The mean concentrations were 5.39 ng/mg (range: 0.43-8.98 ng/mg) for cocaine and 1.11 ng/mg (range: 0.42-2.23 ng/mg) for cocaethylene.

摘要

建立了一种同时测定人发中可卡因(COC)和可口卡因(CE)的方法,采用固相微萃取(SPME)和气相色谱-质谱联用(GC-MS)作为分析技术来鉴定和定量这些药物。采用选择离子监测(SIM)模式以获得更高的灵敏度。使用氘代标记类似物作为内标。在所研究的药物浓度范围为0.4 - 15 ng/mg时,检测器响应呈线性,相关系数高于0.995。变异系数在0.65%至14.18%之间波动,准确度在0.73%至11.20%范围内。定量限和检测限被认为是可接受的。最后,该方法应用于15份来自可卡因使用者的毛发样本,所有样本均得到阳性结果。可卡因的平均浓度为5.39 ng/mg(范围:0.43 - 8.98 ng/mg),可口卡因的平均浓度为1.11 ng/mg(范围:0.42 - 2.23 ng/mg)。

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