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采用分子印迹固相萃取(MISPE)和液相色谱-串联质谱(LC-MS/MS)分析毛发样本中的氯胺酮和去甲氯胺酮。

Analysis of ketamine and norketamine in hair samples using molecularly imprinted solid-phase extraction (MISPE) and liquid chromatography-tandem mass spectrometry (LC-MS/MS).

机构信息

Forensic Medicine and Science, Division of Cancer Sciences and Molecular Pathology, Faculty of Medicine, University of Glasgow, Glasgow G12 8QQ, UK.

出版信息

Anal Bioanal Chem. 2010 Apr;396(7):2449-59. doi: 10.1007/s00216-009-3404-6. Epub 2010 Jan 19.

Abstract

An anti-ketamine molecularly imprinted polymer (MIP) was synthesized and used as the sorbent in a solid-phase extraction protocol to isolate ketamine and norketamine from human hair extracts prior to LC-MS/MS analysis. Under optimised conditions, the MIP was capable of selectively rebinding ketamine, a licensed anaesthetic that is widely misused as a recreational drug, with an apparent binding capacity of 0.13 microg ketamine per mg polymer. The limit of detection (LOD) and lower limit of quantification (LLOQ) for both ketamine and norketamine were 0.1 ng/mg hair and 0.2 ng/mg hair, respectively, when 10 mg hair were analysed. The method was linear from 0.1 to 10 ng/mg hair, with correlation coefficients (R(2)) of better than 0.99 for both ketamine and norketamine. Recoveries from hair samples spiked with ketamine and norketamine at a concentration of 50 ng/mg were 86% and 88%, respectively. The method showed good intra- and interday precisions (<5%) for both analytes. Minimal matrix effects were observed during the LC-MS/MS analysis of ketamine (ion suppression -6.8%) and norketamine (ion enhancement +0.2%). Results for forensic case samples demonstrated that the method successfully detected ketamine and norketamine concentrations in hair samples with analyte concentrations ranging from 0.2 to 5.7 ng/mg and from 0.1 to 1.2 ng/mg, respectively.

摘要

一种抗氯胺酮分子印迹聚合物(MIP)被合成并用作固相萃取方案中的吸附剂,以在 LC-MS/MS 分析之前从人发提取物中分离氯胺酮和去甲氯胺酮。在优化条件下,MIP 能够选择性地重新结合氯胺酮,氯胺酮是一种被广泛滥用的合法麻醉剂,用作娱乐药物,表观结合能力为每毫克聚合物 0.13 微克氯胺酮。氯胺酮和去甲氯胺酮的检测限(LOD)和定量下限(LLOQ)分别为 0.1ng/mg 头发和 0.2ng/mg 头发,当分析 10mg 头发时。该方法在 0.1 至 10ng/mg 头发范围内呈线性,氯胺酮和去甲氯胺酮的相关系数(R(2))均大于 0.99。在浓度为 50ng/mg 的头发样品中添加氯胺酮和去甲氯胺酮的回收率分别为 86%和 88%。该方法对内源性和日间精密度均表现出良好的精密度(<5%)。在 LC-MS/MS 分析氯胺酮(离子抑制-6.8%)和去甲氯胺酮(离子增强+0.2%)过程中观察到最小的基质效应。法医案例样本的结果表明,该方法成功地检测到头发样本中的氯胺酮和去甲氯胺酮浓度,分析物浓度范围分别为 0.2 至 5.7ng/mg 和 0.1 至 1.2ng/mg。

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