Predicting drug penetration across the blood-brain barrier: comparison of micellar liquid chromatography and immobilized artificial membrane liquid chromatography

被引:31
作者
De Vrieze, Mike [1 ]
Lynen, Frederic [1 ]
Chen, Kai [1 ]
Szucs, Roman [2 ]
Sandra, Pat [1 ,3 ]
机构
[1] Univ Ghent, Dept Organ Chem, Separat Sci Grp, B-9000 Ghent, Belgium
[2] Pfizer Global R&D, Sandwich CT13 9NJ, Kent, England
[3] RIC, B-8500 Kortrijk, Belgium
关键词
Blood-brain barrier; Central nervous system; Micellar liquid chromatography; Immobilized artificial membrane; Modeling; IN-SILICO PREDICTION; PERMEABILITY; DESCRIPTORS; MODELS;
D O I
10.1007/s00216-013-7015-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Several in vitro methods have been tested for their ability to predict drug penetration across the blood-brain barrier (BBB) into the central nervous system (CNS). In this article, the performance of a variety of micellar liquid chromatographic (MLC) methods and immobilized artificial membrane (IAM) liquid chromatographic approaches were compared for a set of 45 solutes. MLC measurements were performed on a C-18 column with sodium dodecyl sulfate (SDS), polyoxyethylene (23) lauryl ether (Brij35), or sodium deoxycholate (SDC) as surfactant in the micellar mobile phase. IAM liquid chromatography measurements were performed with Dulbecco's phosphate-buffered saline (DPBS) and methanol as organic modifier in the mobile phase. The corresponding retention and computed descriptor data for each solute were used for construction of models to predict transport across the blood-brain barrier (log BB). All data were correlated with experimental log BB values and the relative performance of the models was studied. SDS-based models proved most suitable for prediction of log BB values, followed closely by a simplified IAM method, in which it could be observed that extrapolation of retention data to 0 % modifier in the mobile phase was unnecessary.
引用
收藏
页码:6029 / 6041
页数:13
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