转铁蛋白
转铁蛋白受体
血脑屏障
脂质体
化学
抗体
生物物理学
内吞作用
靶向给药
受体
药物输送
共轭体系
受体介导的内吞作用
细胞生物学
生物化学
医学
免疫学
生物
神经科学
中枢神经系统
有机化学
聚合物
作者
Maj Schneider Thomsen,Kjeld Johnsen,Krzysztof Kucharz,Martin Lauritzen,Torben Moos
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2022-10-19
卷期号:14 (10): 2237-2237
被引量:30
标识
DOI:10.3390/pharmaceutics14102237
摘要
The blood-brain barrier (BBB), built by brain endothelial cells (BECs), is impermeable to biologics. Liposomes and other nanoparticles are good candidates for the delivery of biologics across the BECs, as they can encapsulate numerous molecules of interest in an omnipotent manner. The liposomes need attachment of a targeting molecule, as BECs unfortunately are virtually incapable of uptake of non-targeted liposomes from the circulation. Experiments of independent research groups have qualified antibodies targeting the transferrin receptor as superior for targeted delivery of nanoparticles to BECs. Functionalization of nanoparticles via conjugation with anti-transferrin receptor antibodies leads to nanoparticle uptake by endothelial cells of both brain capillaries and post-capillary venules. Reducing the density of transferrin receptor-targeted antibodies conjugated to liposomes limits uptake in BECs. Opposing the transport of nanoparticles conjugated to high-affine anti-transferrin receptor antibodies, lowering the affinity of the targeting antibodies or implementing monovalent antibodies increase uptake by BECs and allows for further transport across the BBB. The novel demonstration of transport of targeted liposomes in post-capillary venules from blood to the brain is interesting and clearly warrants further mechanistic pursuit. The recent evidence for passing targeted nanoparticles through the BBB shows great promise for future drug delivery of biologics to the brain.
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