首页> 外文期刊>Journal of the American Society for Mass Spectrometry >Application of parallel liquid chromatography/mass spectrometry for high throughput microsomal stability screening of compound libraries
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Application of parallel liquid chromatography/mass spectrometry for high throughput microsomal stability screening of compound libraries

机译:并行液相色谱/质谱法在化合物库高通量微粒体稳定性筛选中的应用

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Solution-phase and solid-phase parallel synthesis and high throughput screening have enabled biologically active and selective compounds to be identified at an unprecedented rate. The challenge has been to convert these hits into viable development candidates. To accelerate the conversion of these hits into lead development candidates, early assessment of the physicochemical and pharmacological properties of these compounds is being made. In particular, in vitro absorption, distribution, metabolism, and elimination (ADME) assays are being conducted at earlier and earlier stages of discovery with the goal of reducing the attrition rate of these potential drug candidates as they progress through development. In this report, we present an eight-channel parallel liquid chromatography/mass spectrometry (LC/MS) system in combination with custom Visual Basic and Applescript automated data processing applications for high throughput early ADME. The parallel LC/MS system was configured with one set of gradient LC pumps and an eight-channel multiple probe autosampler. The flow was split equivalently into eight streams before the multiple probe autosampler and recombined after the eight columns and just prior to the mass spectrometer ion source. The system was tested for column-to-column variation and for reproducibility over a 17 h period (approximately 500 injections per column). The variations in retention time and peak area were determined to be less than 2 and 10%, respectively, in both tests. The parallel LC/MS system described permits time-course microsomal incubations (t(o), t(5) t(15), t(30)) to be measured in triplicate and enables estimations of t(1/2) microsomal stability. The parallel LC/MS system is capable of analyzing up to 240 samples per hour and permits the complete profiling up to two microtiter plates of compounds per day (i.e., 176 test substrate compounds + sixteen controls). [References: 28]
机译:溶液相和固相平行合成以及高通量筛选使生物活性和选择性化合物得以空前的鉴定。面临的挑战是将这些成功案例转化为可行的发展候选方案。为了加速将这些命中物转化为潜在的候选物,正在对这些化合物的理化和药理特性进行早期评估。尤其是,在发现的早期和较早阶段进行了体外吸收,分布,代谢和消除(ADME)分析,目的是随着这些潜在候选药物的发展逐步减少其消耗率。在此报告中,我们介绍了八通道并行液相色谱/质谱(LC / MS)系统,结合了自定义Visual Basic和Applescript自动化数据处理应用程序,可实现高通量早期ADME。并行LC / MS系统配置有一组梯度LC泵和一个八通道多探针自动进样器。在多探针自动进样器之前,将流等效地分成八股流,并在八根色谱柱之后和质谱仪离子源之前重新合并。测试该系统的色谱柱间差异以及在17小时内的重现性(每根色谱柱约500次进样)。在两个测试中,保留时间和峰面积的变化分别确定为小于2%和10%。所描述的并行LC / MS系统允许一式三份测量时间过程的微粒体温育(t(o),t(5),t(15),t(30)),并能够估算t(1/2)微粒体的稳定性。并行LC / MS系统每小时能够分析多达240个样品,并且每天最多可对两个化合物的微量滴定板进行完整分析(即176个测试底物化合物+ 16个对照)。 [参考:28]

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