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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development of a micropulverized extraction method for rapid toxicological analysis of methamphetamine in hair
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Development of a micropulverized extraction method for rapid toxicological analysis of methamphetamine in hair

机译:微粉萃取法用于头发中甲基苯丙胺的快速毒理分析的开发

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We developed a rapid sample preparation method for the toxicological analysis of methamphetamine and amphetamine (the major metabolite of methamphetamine) in human hair by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS), to facilitate fast screening and quantitation. Two milligrams of hair were mechanically micropulverized for 5 min in a 2-ml plastic tube together with 100 mu l of an aqueous solvent containing 10% acetonitrile, 100 mM trifluoroacetic acid and the corresponding deuterium analogues as internal standards. The pulverizing highly disintegrated the hair components, simultaneously allowing the extraction of any drugs present in the hair. After filtering the suspension with a membrane-filter unit, the clear filtrate was directly analyzed by HPLC-MS/MS. No evaporation processes were required for sample preparation. Method optimization and validation study were carried out using real-case specimens and fortified samples in which the drugs had been artificially absorbed, respectively. Concentration ranges for quantitation were 0.040-125 and 0.040-25 ng/mg for methamphetamine and amphetamine, respectively. Real-case specimens were analyzed by the method presented here and by conventional ones to verify the applicability of our method to real-world analysis. Our method took less than 30 min for a set of chromatograms to be obtained from a washed hair sample. (C) 2007 Elsevier B.V. All rights reserved.
机译:我们开发了一种通过高效液相色谱-串联质谱(HPLC-MS / MS)对人发中的甲基苯丙胺和苯丙胺(甲基苯丙胺的主要代谢产物)进行毒理学分析的快速样品前处理方法,以促进快速筛选和定量。将两毫克的头发与100毫升的含10%乙腈,100毫米三氟乙酸和相应的氘代类似物作为内标的水性溶剂一起在2毫升塑料管中进行机械微粉碎5分钟。粉碎后的头发成分高度崩解,同时允许提取存在于头发中的任何药物。用膜滤器过滤悬浮液后,直接用HPLC-MS / MS分析澄清的滤液。样品制备不需要任何蒸发过程。方法的优化和验证研究分别使用实际情况下的样本和人工吸收了药物的强化样本进行。甲基苯丙胺和苯丙胺的定量浓度范围分别为0.040-125和0.040-25 ng / mg。通过此处介绍的方法和常规方法分析了真实案例的标本,以验证我们的方法在真实世界分析中的适用性。从洗过的头发样品中获得一套色谱图,我们的方法花费了不到30分钟的时间。 (C)2007 Elsevier B.V.保留所有权利。

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