Calcium Condensation of DNA Complexed with Cell-Penetrating Peptides Offers Efficient, Noncytotoxic Gene Delivery

被引:32
作者
Baoum, Abdulgader A. [1 ]
Berkland, Cory [1 ,2 ]
机构
[1] Univ Kansas, Dept Pharmaceut Chem, Lawrence, KS 66045 USA
[2] Univ Kansas, Dept Chem & Petr Engn, Lawrence, KS 66045 USA
关键词
gene delivery; plasmid DNA; cell-penetrating peptides; A549; cells; stability; nanoparticles; cytotoxicity; LOW-MOLECULAR-WEIGHT; CARBOHYDRATE-CONTAINING POLYCATIONS; HIV-1 TAT PROTEIN; NONVIRAL VECTOR; TRANSFECTION; POLYETHYLENIMINE; SYSTEMS; POLY(ETHYLENIMINE); POLYMERIZATION; BIOMATERIALS;
D O I
10.1002/jps.22407
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Drug delivery strategies using cell-penetrating peptides (CPPs) have been widely explored to improve the intracellular delivery of a large number of cargo molecules. Electrostatic complexation of plasmid DNA using CPPs has been less explored due to the relatively large complexes formed and the low levels of gene expression achieved when using these low-molecular-weight polycations as DNA condensing agents. Here, condensing nascent CPP polyplexes using CaCl2 produced small and stable nanoparticles leading to gene expression levels higher than observed for control polyethylenimine gene vectors. This simple formulation approach showed negligible cytotoxicity in A549 lung epithelial cells and maintained particle size and transfection efficiency even in the presence of serum. (C) 2010Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 100:1637-1642, 2011
引用
收藏
页码:1637 / 1642
页数:6
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