Opinion - Carrier-mediated cellular uptake of pharmaceutical drugs: an exception or the rule?

被引:356
作者
Dobson, Paul D. [1 ,2 ]
Kell, Douglas B. [1 ,2 ]
机构
[1] Univ Manchester, Sch Chem, Manchester M1 7DN, Lancs, England
[2] Univ Manchester, Manchester Interdisciplinary Bioctr, Manchester M1 7DN, Lancs, England
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1038/nrd2438
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
It is generally thought that many drug molecules are transported across biological membranes via passive diffusion at a rate related to their lipophilicity. However, the types of biophysical forces involved in the interaction of drugs with lipid membranes are no different from those involved in their interaction with proteins, and so arguments based on lipophilicity could also be applied to drug uptake by membrane transporters or carriers. In this article, we discuss the evidence supporting the idea that rather than being an exception, carrier-mediated and active uptake of drugs may be more common than is usually assumed - including a summary of specific cases in which drugs are known to be taken up into cells via defined carriers - and consider the implications for drug discovery and development.
引用
收藏
页码:205 / 220
页数:16
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