A unique and highly efficient non-viral DNA/siRNA delivery system based on PEI-bisepoxide nanoparticles

被引:66
|
作者
Swami, Archana [1 ]
Kurupati, Raj K. [1 ]
Pathak, Atul [1 ]
Singh, Y. [1 ]
Kumar, P. [1 ]
Gupta, K. C. [1 ]
机构
[1] Delhi Univ Campus, Inst Genom & Integrat Biol, Delhi 110007, India
关键词
nanoparticles; polyethylenimine; transfection; cytotoxicity; siRNA; buffering capacity; bisepoxide;
D O I
10.1016/j.bbrc.2007.08.073
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Delivery of DNA and siRNA into mammalian cells is a powerful technique in treating various diseases caused by single gene defects. Herein, we report a highly efficient delivery system using 1,4-butanediol diglycidyl ether (bisepoxide) crosslinked polyethylenimine (PEI) nanoparticles (PN). The nanoparticle/DNA complexes (nanoplexes) exibited similar to 2.5- to 5.0-fold gene transfer efficacy and decreased cytotoxicity in cultured cell lines, compared to the native PEI (25 kDa) (gold standard) and commercially available transfection agents such as Lipofectamine 2000 and Fugene. The bisepoxide crosslinking results in change in amine ratio in PEI; however, it retains the net charge on PN unaltered. A series of nanoparticles obtained by varying the degree of crosslinking was found to be in the size range of 69-77 nm and the zeta potential varying from +35 to 40 mV. The proposed system was also found to deliver siRNA efficiently into HEK cells, resulting in similar to 70% suppression of the targetted gene (GFP). (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:835 / 841
页数:7
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