Minimum Transendothelial Electrical Resistance Thresholds for the Study of Small and Large Molecule Drug Transport in a Human in Vitro Blood-Brain Barrier Model

被引:62
作者
Mantle, Jennifer L.
Min, Lie
Lee, Kelvin H. [1 ]
机构
[1] Univ Delaware, Dept Chem & Biomol Engn, 15 Innovat Way, Newark, DE 19711 USA
基金
美国国家科学基金会;
关键词
blood-brain barrier; drug transport; human induced pluripotent stem cells; IgG transport; human brain microvascular endothelial cells; Alzheimer's disease; CELLS; PERMEABILITY; OPTIMIZATION; DERIVATION; CULTURE;
D O I
10.1021/acs.molpharmaceut.6b00818
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
A human cell-based in vitro model that can accurately predict drug penetration into the brain as well as metrics to assess these in vitro models are valuable for the development of new therapeutics. Here, human induced pluripotent stem cells (hPSCs) are differentiated into a polarized monolayer that express blood brain barrier (BBB)-specific proteins and have transendothelial electrical resistance (TEER) values greater than 2500 Omega.cm(2). By assessing the permeabilities of several known drugs, a benchmarking system to evaluate brain permeability of drugs was established. Furthermore, relationships between TEER and permeability to both small and large molecules were established, demonstrating that different minimum TEER thresholds must be achieved to study the brain transport of these two classes of drugs. This work demonstrates that this hPSC-derived BBB model exhibits an in vivo-like phenotype, and the benchmarks established here are useful for assessing functionality of other in vitro BBB models.
引用
收藏
页码:4191 / 4198
页数:8
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