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Drug Discovery and Regulatory Considerations for Improving In Silico and In Vitro Predictions that Use Caco-2 as a Surrogate for Human Intestinal Permeability Measurements
被引:109
作者:
Larregieu, Caroline A.
[1
,2
]
Benet, Leslie Z.
[1
,2
]
机构:
[1] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, Sch Pharm, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, Sch Med, San Francisco, CA 94143 USA
来源:
AAPS JOURNAL
|
2013年
/
15卷
/
02期
关键词:
Biopharmaceutics Classification System (BCS);
biowaiver;
Caco-2;
cells;
Food and Drug Administration (FDA);
human intestinal permeability;
in silico modeling;
in vitro screening;
ORGANIC ANION TRANSPORTERS;
POLAR SURFACE-AREA;
WEAKLY BASIC DRUGS;
CELL-PERMEABILITY;
ORAL ABSORPTION;
MEMBRANE-PERMEABILITY;
SIMPLE PARAMETERS;
P-GLYCOPROTEIN;
GASTROINTESTINAL ABSORPTION;
H-2-RECEPTOR ANTAGONISTS;
D O I:
10.1208/s12248-013-9456-8
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
There is a growing need for highly accurate in silico and in vitro predictive models to facilitate drug discovery and development. Results from in vitro permeation studies across the Caco-2 cell monolayer are commonly used for drug permeability screening in industry and are also accepted as a surrogate for human intestinal permeability measurements by the US FDA to support new drug applications. Countless studies carried out in this cell line with published permeability measurements have enabled the development of many in silico prediction models. We identify several common cases that illustrate how using Caco-2 permeability measurements in these in silico and in vitro predictive models will not correlate with human intestinal permeability and will further lead to inaccuracies in these models. We provide guidelines and recommendations for improving these models to more accurately predict clinically relevant information, thereby enhancing the drug discovery, development, and regulatory approval processes.
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页码:483 / 497
页数:15
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