Targeting Brain Drug Delivery with Macromolecules Through Receptor-Mediated Transcytosis

被引:0
|
作者
Li, Yuanke [1 ]
Liu, Ruiying [2 ]
Zhao, Zhen [3 ]
机构
[1] Nankai Univ, Coll Life Sci, Frontiers Sci Ctr Cell Responses, State Key Lab Med Chem Biol,Key Lab Bioact Mat,Min, Tianjin 300071, Peoples R China
[2] Nankai Univ, TEDA Inst Biol Sci & Biotechnol, Natl Key Lab Intelligent Tracking & Forecasting In, Tianjin 300457, Peoples R China
[3] Hebei Univ Technol, Sch Hlth Sci & Biomed Engn, Inst Biophys, Key Lab Mol Biophys, Tianjin 300401, Peoples R China
基金
中国国家自然科学基金;
关键词
receptor-mediated transcytosis; CNS; ligands; antibody; peptide; aptamer; drug delivery; NEUTRON-CAPTURE THERAPY; AMINO-ACID TRANSPORTER; NEONATAL FC-RECEPTOR; POLYMERIC MICELLES; APOLIPOPROTEIN-E; IN-VITRO; GLUCOSE-TRANSPORTER; SCAVENGER RECEPTORS; ANTITUMOR-ACTIVITY; PEPTIDE;
D O I
10.3390/pharmaceutics17010109
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Brain diseases pose significant treatment challenges due to the restrictive nature of the blood-brain barrier (BBB). Recent advances in targeting macromolecules offer promising avenues for overcoming these obstacles through receptor-mediated transcytosis (RMT). We summarize the current progress in targeting brain drug delivery with macromolecules for brain diseases. This exploration details the transport mechanisms across the BBB, focusing on RMT and its use of natural ligands for drug delivery. Furthermore, the review examines macromolecular ligands such as antibodies, peptides, and aptamers that leverage RMT for effective BBB traversal. Advancements in macromolecules-based delivery systems for brain diseases are summarized, emphasizing their therapeutic potential and limitations. Finally, emerging RMT strategies, including viral vectors, exosomes, and boron neutron capture therapy, are discussed for their precision in brain-targeted treatments. This comprehensive overview underscores the potential of RMT-based approaches to revolutionize brain disease therapy.
引用
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页数:26
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