Ackermann Bradley L, Berna Michael J, Murphy Anthony T
Department of Lead Optimization and Drug Disposition, Lilly Research Laboratories, Lilly Corporate Center, Indianapolis, IN 46285, USA.
Curr Top Med Chem. 2002 Jan;2(1):53-66. doi: 10.2174/1568026023394605.
LC/MS/MS based bioanalysis using atmospheric pressure ionization (API)-style interfaces has now been applied for over a decade. This technology, which initially found application for clinical bioanalysis, is now firmly established as the primary bioanalytical tool for ADME studies related to drug discovery and lead optimization (LO). This review focuses on recent advances in LC/MS/MS based bioanalysis in support of drug discovery and LO. The initial part of the article reviews the principal components of LC/MS/MS bioanalysis: sample preparation, chromatography, ionization and mass analysis. In each section, factors affecting high throughput bioanalysis are addressed. Because of the importance of on-line column switching methods to discovery bioanalysis, the section on sample preparation is divided into off-line and on-line approaches. In addition, the discussion of chromatography is limited to reversed phase liquid chromatography with emphasis given to the trend towards high-flow gradient elution techniques. The latter part of the review focuses on considerations for experimental design. In this section, pooling methods such as cassette dosing are discussed along with more highly integrated strategies linking bioanalysis with protocol generation and sample collection. The article concludes by briefly reviewing factors, which affect bioanalytical precision and accuracy, such as ion suppression, analyte stability and metabolite interference.
基于液相色谱串联质谱(LC/MS/MS)并采用大气压电离(API)式接口的生物分析技术已应用了十多年。这项最初应用于临床生物分析的技术,如今已稳固地成为药物发现和先导化合物优化(LO)相关的吸收、分布、代谢和排泄(ADME)研究的主要生物分析工具。本综述聚焦于基于LC/MS/MS的生物分析在支持药物发现和先导化合物优化方面的最新进展。文章开篇部分回顾了LC/MS/MS生物分析的主要组成部分:样品制备、色谱分析、离子化和质量分析。在每个部分中,均探讨了影响高通量生物分析的因素。由于在线柱切换方法对发现生物分析的重要性,样品制备部分分为离线和在线方法。此外,色谱分析的讨论仅限于反相液相色谱,并着重介绍了高流量梯度洗脱技术的发展趋势。综述的后半部分聚焦于实验设计的考量因素。在这一部分,讨论了诸如盒式给药等合并方法,以及将生物分析与方案生成和样品采集相联系的更高整合度策略。文章最后简要回顾了影响生物分析精密度和准确度的因素,如离子抑制、分析物稳定性和代谢物干扰。