首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Development and validation of an analytical method for the simultaneous determination of cocaine and its main metabolite, benzoylecgonine, in human hair by gas chromatography/mass spectrometry
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Development and validation of an analytical method for the simultaneous determination of cocaine and its main metabolite, benzoylecgonine, in human hair by gas chromatography/mass spectrometry

机译:气相色谱/质谱法同时测定人发中可卡因及其主要代谢物苯甲酰芽子碱的分析方法的开发和验证

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摘要

A new, simple and rapid procedure has been developed and validated for the determination of cocaine and its main metabolite, benzoylecgonine, in human hair samples. After extraction from within the hair matrix by a mixture of methanol/hydrochloric acid (2:1) at 65 degrees C for 3 h, and sample cleanup by mixed-mode solid-phase extraction (SPE), the extracts were analyzed by gas chromatography/mass spectrometry (GC/MS), after derivatization with N-methyl-N-(trimethylsilyl)trifluoroacetamide with 5% chlorotrimethylsilane. Using a sample size of only 20 mg of hair, limits of detection (LODs) and quantitation (LOQs) were, respectively, 20 and 50 pg/mg for cocaine, and 15 and 50 pg/mg for benzoylecgonine, achieving the cut-off values proposed by the Society of Hair Testing for the analysis of these compounds in hair. The method was found to be linear (weighing factor of IN) between the LOQ and 20 ng/mg for both compounds, with correlation coefficients ranging from 0.9974 to 0.9996 for cocaine; and from 0.9981 to 0.9994 for benzoylecgonine. Intra- and interday precision and accuracy were in conformity with the criteria normally accepted ill bioanalytical method validation. The sample cleanup step presented a mean absolute recovery greater than 90% for both compounds. The developed method may be useful in forensic toxicology laboratories for the analysis of cocaine and benzoylecgonine in hair samples, taking into account its speed (only 3 h are required for the extraction of the analytes from within the matrix, whereas 5 h or even overnight extractions have been reported) and the low limits achieved (using a single quadrupole mass spectrometer, which is available in most laboratories). Copyright (C) 2008 John Wiley & Sons, Ltd.
机译:已经开发了一种新的,简单而快速的程序,并已用于测定人发样品中的可卡因及其主要代谢物苯甲酰芽子碱。在65°C下用甲醇/盐酸(2:1)的混合物从毛发基质中提取3 h,并通过混合模式固相萃取(SPE)净化样品后,通过气相色谱分析萃取物/ N-甲基-N-(三甲基甲硅烷基)三氟乙酰胺与5%氯三甲基硅烷衍生化后,质谱分析(GC / MS)。使用仅20 mg头发的样本量,可卡因的检出限(LOD)和定量(LOQ)分别为20和50 pg / mg,苯甲酰芽子碱为15和50 pg / mg,达到了临界值头发测试协会提出的用于分析头发中这些化合物的数值。对于两种化合物,该方法在LOQ和20 ng / mg之间呈线性关系(IN的权重因子),可卡因的相关系数范围为0.9974至0.9996。苯甲酰芽子碱从0.9981至0.9994。盘中和盘中的精确度和准确性符合通常在生物分析方法验证中接受的标准。样品净化步骤显示两种化合物的平均绝对回收率均大于90%。考虑到其速度(从基质内部提取分析物只需3小时,而提取5 h甚至连夜提取),开发的方法在法医毒理学实验室中可用于分析头发样品中的可卡因和苯甲酰芽子碱。已报告)和达到的下限(使用单个四极质谱仪,大多数实验室都可以使用)。版权所有(C)2008 John Wiley&Sons,Ltd.

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