Overcoming biological barriers by virus-like drug particles for drug delivery

被引:19
|
作者
Chen, Yu-Ling [1 ,2 ]
Bao, Chun-Jie [1 ,2 ,3 ,4 ]
Duan, Jia-Lun [1 ,2 ,4 ]
Xie, Ying [1 ,2 ]
Lu, Wan-Liang [1 ,2 ]
机构
[1] Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing Key Lab Mol Pharmaceut & Drug Delivery Sys, Beijing 100191, Peoples R China
[2] Peking Univ, Sch Pharmaceut Sci, Beijing 100191, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Med & Holist Integrat Med, Nanjing 210023, Peoples R China
[4] Nanjing Univ Chinese Med, Jiangsu Collaborat Innovat Ctr Chinese Med Resourc, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
Virus -like particles (VLPs); Physiological barriers; Drug delivery; Strategies; MESOPOROUS SILICA NANOPARTICLES; BLOOD-BRAIN-BARRIER; IN-VIVO; MESSENGER-RNA; MOSAIC-VIRUS; ADENOVIRUS DODECAHEDRON; VIRAL NANOPARTICLES; INTRACELLULAR DELIVERY; BASEMENT-MEMBRANE; PLANT-VIRUS;
D O I
10.1016/j.addr.2023.115134
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Virus-like particles (VLPs) have natural structural antigens similar to those found in viruses, making them valuable in vaccine immunization. Furthermore, VLPs have demonstrated significant potential in drug delivery, and emerged as promising vectors for transporting chemical drug, genetic drug, peptide/protein, and even nanoparticle drug. With virus-like permeability and strong retention, they can effectively target specific organs, tissues or cells, facilitating efficient intracellular drug release. Further modifications allow VLPs to transfer across various physiological barriers, thus acting the purpose of efficient drug delivery and accurate therapy. This article provides an overview of VLPs, covering their structural classifications, deliverable drugs, potential physiological barriers in drug delivery, strategies for overcoming these barriers, and future prospects.
引用
收藏
页数:22
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