Safe and efficient in vitro and in vivo gene delivery: tripodal cationic lipids with programmed biodegradability

被引:8
|
作者
Unciti-Broceta, Asier [1 ]
Moggio, Loredana
Dhaliwal, Kevin [2 ]
Pidgeon, Laura
Finlayson, Keith
Haslett, Chris [2 ]
Bradley, Mark
机构
[1] Univ Edinburgh, Inst Genet & Mol Med, Edinburgh Canc Res UK Ctr, Sch Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
[2] Univ Edinburgh, MRC Ctr Inflammat Res, Edinburgh EH9 3JJ, Midlothian, Scotland
基金
英国工程与自然科学研究理事会;
关键词
MAMMALIAN-CELLS; GEMINI SURFACTANTS; TRANSFECTION; THERAPY; CARRIERS; DESIGN; DNA; AMPHIPHILES; LIPOSOME; VECTORS;
D O I
10.1039/c0jm03241g
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
The therapeutic use of nucleic acids has long been heralded as a panacea of medicinal opportunity, a vision enhanced by the introduction of RNA interference technology. The Achilles heel of such an approach is the in vivo delivery of the desired nucleic acid into cells, a practice that lacks selectivity, safety and/or efficiency. Herein we report the safe and efficacious in vitro and in vivo delivery of nucleic acids using tripodal biodegradable cationic lipids. Toxicity reduction and transfection potency of these novel amphiphiles were addressed by designing the compounds to undergo complete intracellular degradation thereby enhancing cargo release while minimising toxicity and potential tissue accumulation. Compounds demonstrated high-efficiency in transfecting DNA into cells both in vitro and in vivo with no signs of toxicity, thus potentially offering a safer alternative to viral transfection for gene therapy application.
引用
收藏
页码:2154 / 2158
页数:5
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