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无需样品制备和液相色谱分离,采用实时串联质谱直接分析法定量血浆中的小分子。

Quantification of small molecules in plasma with direct analysis in real time tandem mass spectrometry, without sample preparation and liquid chromatographic separation.

作者信息

Zhao Yeping, Lam Michelle, Wu Danlin, Mak Rowena

机构信息

Department of Drug Metabolism and Pharmacokinetics, Roche Palo Alto, LLC, 3431 Hillview Ave., Palo Alto, CA 94304, USA.

出版信息

Rapid Commun Mass Spectrom. 2008 Oct;22(20):3217-24. doi: 10.1002/rcm.3726.

Abstract

Recently, a new ion source, Direct Analysis in Real Time (DART), has been introduced which allows direct biological sample introduction into a mass spectrometry (MS) system. The elimination of conventionally required sample preparation and separation by high-performance liquid chromatography (HPLC) prior to MS analysis represents a remarkable opportunity to reduce assay turn-around time, environmental impact and capital/manpower investment. This new technology initially was used in various qualitative applications to directly detect chemicals on solid surfaces, in liquids and gases. In this study, a DART source operating under ambient pressure with ground potential was installed onto a Sciex 4000 tandem mass spectrometer and employed in the sample analysis of plasma based on direct introduction into the DART-MS/MS system. Reasonable precision and accuracy (%CV and %Error, both <10%) were achieved of a significant number of compounds tested in biological fluids. In addition, the limit of detection for 80% of the tested compounds reached 5 ng/mL or lower which is sufficient for pharmaceutical drug discovery support. Finally, experimental conditions that significantly impacted assay performance were investigated with respect to optimization and limitation. Because of its simplicity, fast data acquisition (3-5 s) and low cost, DART has the potential to significantly impact quantitative pharmaceutical analysis in biological matrices.

摘要

最近,一种新的离子源——实时直接分析(DART)已被引入,它允许将生物样品直接引入质谱(MS)系统。在质谱分析之前,无需进行传统的样品制备和高效液相色谱(HPLC)分离,这为减少分析周转时间、环境影响以及资本/人力投入提供了一个显著的契机。这项新技术最初用于各种定性应用,以直接检测固体表面、液体和气体中的化学物质。在本研究中,将在常压下以地电位运行的DART源安装到Sciex 4000串联质谱仪上,并基于直接引入DART-MS/MS系统用于血浆的样品分析。对生物流体中大量测试化合物实现了合理的精密度和准确度(%CV和%误差,均<10%)。此外,80%的测试化合物的检测限达到5 ng/mL或更低,这足以支持药物发现。最后,针对优化和局限性研究了对分析性能有显著影响的实验条件。由于其简单性、快速的数据采集(3 - 5秒)和低成本,DART有可能对生物基质中的定量药物分析产生重大影响。

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