Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Lab Chip. 2018 Jun 26;18(13):1831-1837. doi: 10.1039/c8lc00039e.
Microphysiological systems (MPS) hold promise for improving therapeutic drug approval rates by providing more physiological, human-based, in vitro assays for preclinical drug development activities compared to traditional in vitro and animal models. Here, we first summarize why MPSs are needed in pharmaceutical development, and examine how MPS technologies can be utilized to improve preclinical efforts. We then provide the perspective that the full impact of MPS technologies will be realized only when robust approaches for in vitro-in vivo (MPS-to-human) translation are developed and utilized, and explain how the burgeoning field of quantitative systems pharmacology (QSP) can fill that need.
微生理系统(MPS)有望通过为临床前药物开发活动提供更具生理意义、基于人体的体外检测方法,改善治疗药物批准率,与传统的体外和动物模型相比。在这里,我们首先总结了为什么在药物开发中需要 MPS,并探讨了如何利用 MPS 技术来改善临床前工作。然后我们提出了这样的观点,即只有当开发和利用了体外-体内(MPS 到人体)转化的强大方法时,MPS 技术的全部影响才会显现出来,并解释了新兴的定量系统药理学(QSP)领域如何满足这一需求。