Self-Assembled Lipid Nanomedicines for siRNA Tumor Targeting

被引:31
作者
Tseng, Yu-Cheng [1 ]
Huang, Leaf [1 ]
机构
[1] Univ N Carolina, Div Mol Pharmaceut, Sch Pharm, Chapel Hill, NC 27599 USA
关键词
Self-Assembly; Lipid; Liposome; Nanoparticles; Nanomedicine; siRNA; Tumor Targeting; Endosome Escape; CFTR GENE-TRANSFER; LIPOSOMAL DOXORUBICIN DOXIL; MEDIATED DNA-TRANSFECTION; IN-VIVO; RNA INTERFERENCE; DRUG-DELIVERY; SYSTEMIC DELIVERY; HIGHLY EFFICIENT; STEALTH LIPOSOMES; NASAL EPITHELIUM;
D O I
10.1166/jbn.2009.1044
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Lipid-based nanoparticle technology has developed from chemical drug carrier into an efficient multifunctional siRNA tumor targeting delivery system. In this review, we start with an overview of the lipid-based nanomedicine history and the two classes of lipidic vectors for DNA or siRNA delivery. Then we discuss the features of lipid-based nanomedicine that lead to effective tumor targeting and the principles behind. We also discuss nanoparticle surface modification, classes of tumor targeting ligands, and other state-of-the-art strategies for enhancing endosome release primarily focused on lipid-based systems. At the end, we show that multifunctional self-assembled lipid-based nanoparticles could also be versatile delivery vehicles for cancer molecular imaging probes.
引用
收藏
页码:351 / 363
页数:13
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