The effect of plasma protein binding on in vivo efficacy: misconceptions in drug discovery

被引:655
作者
Smith, Dennis A. [2 ]
Di, Li [1 ]
Kerns, Edward H. [3 ]
机构
[1] Pfizer Global Res & Dev, Pharmacokinet Dynam & Metab Dept, Groton, CT 06340 USA
[2] Pfizer Global Res & Dev, Pharmacokinet Dynam & Metab Dept, Sandwich CT13 9UJ, Kent, England
[3] Discovery ADME, Skillman, NJ 08558 USA
关键词
BLOOD-BRAIN-BARRIER; DISPLACEMENT INTERACTIONS; CLINICAL PHARMACOKINETICS; ANTIVIRAL ACTIVITY; RECEPTOR; PREDICTION; PENETRATION; FLUCONAZOLE; INHIBITORS; MECHANISM;
D O I
10.1038/nrd3287
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Data from in vitro plasma protein binding experiments that determine the fraction of protein-bound drug are frequently used in drug discovery to guide structure design and to prioritize compounds for in vivo studies. However, we consider that these practices are usually misleading, because in vivo efficacy is determined by the free (unbound) drug concentration surrounding the therapeutic target, not by the free drug fraction. These practices yield no enhancement of the in vivo free drug concentration. So, decisions based on free drug fraction could result in the wrong compounds being advanced through drug discovery programmes. This Perspective provides guidance on the application of plasma protein binding information in drug discovery.
引用
收藏
页码:929 / 939
页数:12
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