4.7 Article Proceedings Paper

An automated method for measurement of methoxetamine in human plasma by use of turbulent flow on-line extraction coupled with liquid chromatography and mass spectrometric detection

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 405, 期 1, 页码 239-245

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-012-6470-0

关键词

Designer drugs; Methoxetamine; On-line extraction; LC-MS-MS

向作者/读者索取更多资源

Methoxetamine is a new ketamine derivative designer drug which has recently become available via the Internet marketed as legal ketamine. It is a new dissociative recreational drug, acting as an NMDA receptor antagonist and dopamine reuptake inhibitor. The objective of this study was to develop on-line automated sample preparation using a TurboFlow device coupled with liquid chromatography with ion-trap mass spectrometric detection for measurement of methoxetamine in human plasma. Samples (100 mu L) were vortex mixed with internal standard solution (ketamine-d4 in acetonitrile). After centrifugation, 20 mu L of the supernatant was injected on to a 50 mm x 0.5-mm C18XL Turboflow column. The retained analytes were then back-flushed on to a 50 mm x 3-mm (3 mu m) Hypersil Gold analytical column for chromatographic separation, then eluted with a formate buffer-acetonitrile gradient. Methoxetamine and the IS were ionized by electrospray in positive mode. Parent [M + H](+) ions were m/z 248.1 for methoxetamine and m/z 242.0 for the IS. The most intense product ions from methoxetamine (m/z 203.0) and the IS (m/z 224.0) were used for quantification. The assay was accurate (96.8-108.8 % range) and precise (intra and inter-day coefficients of variation < 8.8 %) over the range of 2.0 (lower limit of quantification) to 1000.0 ng mL(-1) (upper limit of quantification). No matrix effect was observed. This method has been successfully applied to determination of plasma concentrations of methoxetamine in the first French hospitalization case report after acute intoxication; the plasma concentration was 136 ng mL(-1).

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据