Davies Geraint
Institutes of Infection and Global Health and of Translational Medicine, University of Liverpool, Liverpool L69 7BE, United Kingdom.
Cold Spring Harb Perspect Med. 2014 Sep 18;5(1):a021170. doi: 10.1101/cshperspect.a021170.
Rational development and deployment of antituberculosis drugs depend on a comprehensive understanding of the pharmacokinetics and pharmacodynamics that underlie their clinical behavior. Successful implementation of a pharmacokinetic-pharmacodynamic approach faces difficulties that, although not unique to tuberculosis as a therapeutic area, in combination pose a significant scientific challenge. In recent years, a multidisciplinary response combining new technological and analytical approaches has begun to directly address many of these issues, shedding light on some previously poorly understood aspects of drug distribution and response. These advances have important implications for optimization of existing and development of novel drug regimens, putting quantitative pharmacology at the heart of preclinical and early drug development.
抗结核药物的合理研发与应用依赖于对其临床行为背后的药代动力学和药效动力学的全面理解。药代动力学-药效动力学方法的成功应用面临一些困难,尽管这些困难并非结核病治疗领域所独有,但综合起来构成了重大的科学挑战。近年来,结合新技术和分析方法的多学科应对措施已开始直接解决其中许多问题,为药物分布和反应的一些先前了解不足的方面带来了新的认识。这些进展对现有药物方案的优化和新型药物方案的研发具有重要意义,使定量药理学成为临床前和早期药物研发的核心。