Intelligent nucleic acid delivery systems based on stimuli-responsive polymers

被引:76
作者
Du, Fu-Sheng [1 ]
Wang, Yang [1 ]
Zhang, Rui [1 ]
Li, Zi-Chen [1 ]
机构
[1] Peking Univ, BNLMS, Key Lab Polymer Chem & Phys,Minist Educ, Dept Polymer Sci & Engn,Coll Chem & Mol Engn, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
NONVIRAL GENE DELIVERY; POLYELECTROLYTE COMPLEX MICELLES; LOW-MOLECULAR-WEIGHT; POLY(ETHYLENE GLYCOL)-SIRNA CONJUGATE; CATIONIC FUSOGENIC PEPTIDE; EFFICIENT SIRNA DELIVERY; SMALL INTERFERING RNA; PLASMID DNA DELIVERY; IN-VIVO; DRUG-DELIVERY;
D O I
10.1039/b915020j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Despite significant advances in the past two decades, gene therapy is still in the stage of clinical trials worldwide mainly due to the lack of safe and efficient delivery vehicles for therapeutic nucleic acids. Among the various attempts to develop clinically applicable gene therapy, polymer-based nucleic acid delivery systems have attracted great interest, especially for the exciting RNAi-based gene therapy. Regarding in vivo nucleic acid delivery, in particular via intravenous injection, there are many extraand intracellular obstacles, some of which are conflicting. Virus-mimicking nucleic acid delivery systems that combine multiple and programmable functions are thought to be very promising for conquering these challenging barriers. In this review article, we highlight recent progress in stimuli-responsive polymers that have been applied in fabrication of non-viral multi-functional nucleic acid vehicles, which are categorized by the type of stimulus: reduction potential, pH, temperature, and others. In each section, intelligent pDNA delivery systems are introduced first, followed by summarizing various responsive polymer-based siRNA vehicles. Considering the great potential of RNAi-based gene therapy, we devote some space to the recent progress of multi-functional siRNA delivery systems. In addition, different requirements in designing polymer-based siRNA and pDNA carriers are also specified in this review.
引用
收藏
页码:835 / 848
页数:14
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