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采用薄层色谱-串联质谱法测定生物样品中的药物。

Determination of drugs in biological samples by thin-layer chromatography-tandem mass spectrometry.

作者信息

Henion J, Maylin G A, Thomson B A

出版信息

J Chromatogr. 1983 Apr 22;271(1):107-24. doi: 10.1016/s0021-9673(00)80203-4.

Abstract

In this work thin-layer chromatography-tandem mass spectrometry (TLC-MS-MS) allowed detection and confirmation of caffeine and nicotine in human urine and of butorphanol, betamethasone, and clenbuterol in equine urine. In most cases of trace analysis of labile compounds the drugs could not be identified unless they were developed on a TLC plate, scraped from the plate and the TLC scrape eluted with a suitable organic solvent prior to MS-MS. Usually a sample prepared in this way still had several components in it, but was sufficiently cleaned up to allow collision-induced dissociation (CID) experiments to unequivocally identify the drug. In contrast, trace levels of labile drugs could not be identified by CID experiments either directly from the raw urine extracts or by thermally desorbing them from the TLC scrape.

摘要

在本研究中,薄层色谱-串联质谱法(TLC-MS-MS)可检测并确证人体尿液中的咖啡因和尼古丁,以及马尿液中的布托啡诺、倍他米松和克伦特罗。在大多数不稳定化合物痕量分析的案例中,除非将药物在薄层色谱板上展开,从板上刮下并在进行串联质谱分析之前用合适的有机溶剂洗脱薄层色谱刮屑,否则无法识别这些药物。通常,以这种方式制备的样品中仍含有几种成分,但已充分净化,足以进行碰撞诱导解离(CID)实验以明确鉴定药物。相比之下,无论是直接从原始尿液提取物中,还是通过从薄层色谱刮屑中进行热脱附,都无法通过CID实验鉴定痕量的不稳定药物。

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