Advancing nonviral gene delivery: lipid- and surfactant-based nanoparticle design strategies

被引:10
作者
Donkuru, McDonald [1 ]
Badea, Ildiko [1 ]
Wettig, Shawn [2 ]
Verrall, Ronald [3 ]
Elsabahy, Mahmoud [2 ]
Foldvari, Marianna [1 ,2 ]
机构
[1] Univ Saskatchewan, Coll Pharm & Nutr, Saskatoon, SK S7N 5C9, Canada
[2] Univ Waterloo, Sch Pharm, Fac Sci, Waterloo, ON N2L 3G1, Canada
[3] Univ Saskatchewan, Dept Chem, Saskatoon, SK S7N 5C9, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
active targeting; DNA; gemini surfactant; gene therapy; lipoplexes; nonviral delivery systems; soft nanoparticles; IN-VITRO LIPOFECTION; NUCLEAR-LOCALIZATION SIGNALS; LIPOSOME-DNA COMPLEXES; MAMMALIAN-CELLS OCCURS; CATIONIC LIPIDS; TRANSFECTION EFFICIENCY; GEMINI SURFACTANTS; PLASMID DNA; ENDOSOMAL ESCAPE; PHYSICOCHEMICAL CHARACTERIZATION;
D O I
10.2217/NNM.10.80
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Gene therapy is a technique utilized to treat diseases caused by missing, defective or overexpressing genes. Although viral vectors transfect cells efficiently, risks associated with their use limit their clinical applications. Nonviral delivery systems are safer, easier to manufacture, more versatile and cost effective. However, their transfection efficiency lags behind that of viral vectors. Many groups have dedicated considerable effort to improve the efficiency of nonviral gene delivery systems and are investigating complexes composed of DNA and soft materials such as lipids, polymers, peptides, dendrimers and gemini surfactants. The bottom-up approach in the design of these nanoparticles combines components essential for high levels of transfection, biocompatibility and tissue-targeting ability. This article provides an overview of the strategies employed to improve in vitro and in vivo transfection, focusing on the use of cationic lipids and surfactants as building blocks for nonviral gene delivery systems.
引用
收藏
页码:1103 / 1127
页数:25
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