首页> 外文期刊>Journal of Chromatography, Biomedical Applications >Direct cocktail analysis of drug discovery compounds in pooled plasma samples using liquid chromatography-tandem mass spectrometry
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Direct cocktail analysis of drug discovery compounds in pooled plasma samples using liquid chromatography-tandem mass spectrometry

机译:使用液相色谱-串联质谱法对合并血浆样品中的药物发现化合物进行直接鸡尾酒分析

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Direct plasma injection technology coupled with a LC-MS/MS assay provides fast and straightforward method development and greatly reduces the time for the tedious sample preparation procedures. In this work, a simple and sensitive bioanalytical method based on direct plasma injection using a single column high-performance liquid chromatography (HPLC) and tandem mass spectrometry (MS/MS) was developed for direct cocktail analysis of double-pooled mouse plasma samples for the quantitative determination of small molecules. The overall goal was to improve the throughput of the rapid pharmacokinetic (PK) screening process for early drug discovery candidates. Each pooled plasma sample was diluted with working solution containing internal standard and then directly injected into a polymer-coated mixed-function column for sample clean-up, enrichment and chromatographic separation. The apparent on-column recovery of six drug candidates in mouse plasma samples was greater than 90%. The single HPLC column was linked to either an atmospheric pressure chemical ionization (APCI) or electrospray ionization (ESI) source as a part of MS/MS system. The total run cycle time using single column direct injection methods can be achieved within 4 min per sample. The analytical results obtained by the described direct injection methods were comparable with those obtained by semi-automated protein precipitation methods within ±15%. The advantages and challenges of using direct single column LC-MS/MS methods with two ionization sources in combination of sample pooling technique are discussed.
机译:直接血浆注射技术与LC-MS / MS分析相结合,提供了快速直接的方法开发方法,并大大减少了繁琐的样品制备过程的时间。在这项工作中,开发了一种基于单血浆高效液相色谱(HPLC)和串联质谱(MS / MS)的直接血浆注射的简单而灵敏的生物分析方法,用于双池小鼠血浆样品的直接混合物分析。小分子的定量测定。总体目标是提高早期药物发现候选者的快速药代动力学(PK)筛选过程的通量。每个合并的血浆样品用含有内标的工作溶液稀释,然后直接注入到聚合物包被的混合功能色谱柱中,以进行样品净化,富集和色谱分离。小鼠血浆样品中六种候选药物的表观柱上回收率大于90%。单个HPLC色谱柱与作为MS / MS系统一部分的大气压化学电离(APCI)或电喷雾电离(ESI)源相连。每个样品使用单柱直接进样方法的总运行周期时间可以在4分钟内达到。通过所述直接注射方法获得的分析结果与通过半自动蛋白质沉淀法获得的分析结果相差±15%。讨论了使用直接单柱LC-MS / MS方法与两个电离源结合样品合并技术的优缺点。

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