跨细胞
血脑屏障
药物输送
药物输送到大脑
化学
脂质体
生物物理学
阳离子脂质体
薄壁组织
基底膜
中枢神经系统
细胞生物学
纳米载体
吸附
细胞
神经科学
生物化学
内吞作用
生物
医学
遗传增强
病理
基因
有机化学
出处
期刊:Current Pharmaceutical Biotechnology
[Bentham Science]
日期:2012-10-01
卷期号:13 (12): 2340-2348
被引量:79
标识
DOI:10.2174/138920112803341851
摘要
The blood-brain barrier (BBB), which impedes drug penetration into the central nervous system, is composed of specific structures formed by brain capillary endothelial cells and sheathed by astrocytic end-feet through basement membrane. Many brain drug delivery strategies have focused on adsorptive-mediated transcytosis (AMT), which is triggered by electrostatic interaction between cationic molecules and anionic microdomains on the cytoplasm membrane of the brain capillary endothelial cells. AMT-based drug delivery to the brain can be achieved by using cationic proteins and basic oligopeptides such as cell-penetrating peptides as targetors. Large therapeutic molecules such as neuropeptides and proteins or even drug-encapsulated vectors such as liposomes and nanoparticles can be allowed to access brain parenchyma through AMT when conjugated with these cationic targetors. In this review, I briefly discuss adsorptive-mediated brain delivery systems that may provide physiologic-based strategies for enhanced delivery of therapeutic substances through the BBB. Keywords: Adsorptive-mediated transcytosis (AMT), blood-brain barrier (BBB), cationized protein, nanoparticle, toxicity, central nervous system, endothelial cells, adsorptive-mediated transcytosis (AMT), cationic proteins, neuropeptides, brain capillary endothelial cells (BCECs), astrocytic end-feet, Large therapeutic molecules, blood milieu
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