Gu M, Lim H K
Wyeth-Ayerst Research, CN 8000, Princeton, New Jersey 08543, USA.
J Mass Spectrom. 2001 Sep;36(9):1053-61. doi: 10.1002/jms.204.
This paper describes the development of a mass spectrometer-based, intelligent, programmable, sample-selection data acquisition system with two unique features. One is that the system allows automatic determination of the mass to charge ratio (m/z) of an unknown compound and the utilization of the molecular ion information to perform selective ion monitoring (SIM) experiments for quantitation. The other is its decision-making capability to select intelligently different samples and perform different experiments during data acquisition. These features were demonstrated by the application of the system to simultaneous screening for the microsomal stability and metabolite profiling of adatanserin. In this application, the data acquisition system continuously calculated the peak areas of adatanserin from SIM analyses of a batch of microsomal incubates stopped at various time points. Once the peak area of adatanserin had dropped to an arbitrarily predefined 60% of the initial value, the system made a decision to perform metabolite profiling of the sample. This decision initiated a series of automated operations, such as selecting a sample for re-analysis, changing the data acquisition time and liquid chromatographic gradient and switching the SIM mode to the data-dependent product ion scanning mode. The completed analysis of the batch of samples provided information both on the microsomal stability and on the metabolic profile of adatanserin. This simultaneous approach to investigating microsomal stability and metabolite profiling significantly increases the throughput for drug discovery support.
本文描述了一种基于质谱仪的、智能的、可编程的、具有两个独特特征的样品选择数据采集系统的开发。一个特征是该系统允许自动测定未知化合物的质荷比(m/z),并利用分子离子信息进行选择性离子监测(SIM)实验以进行定量分析。另一个特征是其在数据采集过程中能够智能地选择不同样品并进行不同实验的决策能力。通过将该系统应用于同时筛选阿坦色林的微粒体稳定性和代谢物谱,证明了这些特征。在该应用中,数据采集系统通过对在不同时间点终止的一批微粒体孵育物进行SIM分析,持续计算阿坦色林的峰面积。一旦阿坦色林的峰面积降至预先设定的初始值的60%,系统就会决定对该样品进行代谢物谱分析。该决定启动了一系列自动化操作,如选择一个样品进行重新分析、改变数据采集时间和液相色谱梯度,以及将SIM模式切换到数据依赖型产物离子扫描模式。对这批样品的完整分析提供了有关阿坦色林微粒体稳定性和代谢谱的信息。这种同时研究微粒体稳定性和代谢物谱的方法显著提高了药物发现支持的通量。