Biomimetic Chromatography to Accelerate Drug Discovery: Part II

被引:0
|
作者
Valko, Klara [1 ,2 ]
机构
[1] Biomimet Chromatog Ltd, Stevenage, Herts, England
[2] UCL, Sch Pharm, London, England
关键词
LEAD OPTIMIZATION; PHARMACOKINETICS; EFFICIENCY;
D O I
暂无
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The biomimetic gradient retention time measurements on C18, immobilized artificial membrane (IAM), human serum albumin (HSA), and acid-glycoprotein (AGP) stationary phases can be used to characterize compounds partitioning into phospholipids and proteins. The data obtained can then be used in equations to estimate the in vivo plasma-tissue distribution of the compounds measured. The plasma protein binding, brain tissue binding, and in vivo drug efficiency can also be calculated using the biomimetic chromatographic data.
引用
收藏
页码:520 / 526
页数:7
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