Cationic Lipid-Coated Gold Nanoparticles as Efficient and Non-Cytotoxic Intracellular siRNA Delivery Vehicles

ABSTRACT Purpose Cationic lipid-coated gold nanoparticles were developed for efficient intracellular delivery of therapeutic siRNA. Methods Particle formation was characterized by UV-visible spectroscopy, atomic force microscopy, and dynamic light scattering analysis. Cellular uptake, gene silencing...

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Published inPharmaceutical research Vol. 29; no. 2; pp. 362 - 374
Main Authors Kong, Won Ho, Bae, Ki Hyun, Jo, Sung Duk, Kim, Jee Seon, Park, Tae Gwan
Format Journal Article
LanguageEnglish
Published Boston Springer US 01.02.2012
Springer
Springer Nature B.V
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Summary:ABSTRACT Purpose Cationic lipid-coated gold nanoparticles were developed for efficient intracellular delivery of therapeutic siRNA. Methods Particle formation was characterized by UV-visible spectroscopy, atomic force microscopy, and dynamic light scattering analysis. Cellular uptake, gene silencing effect, and cytotoxicity were investigated in multiple human cancer cell lines. Results Nanoparticles had a spherical nanostructure with highly cationic surface charge and could form stable nanosized polyelectrolyte complexes with siRNA via electrostatic interactions; complexes exhibited efficient intracellular uptake and significant gene silencing effect with markedly low cytotoxicity compared to the widely used polycationic carrier, linear polyethyleneimine. Conclusions We demonstrated that cationic lipid-coated gold nanoparticles could be widely utilized as efficient and safe siRNA nanocarriers for diverse therapeutic and diagnostic applications.
ISSN:0724-8741
1573-904X
DOI:10.1007/s11095-011-0554-y