4.6 Article

Poly(L-lactic acid)/polyethylenimine nanoparticles as plasmid DNA carriers

Journal

ARCHIVES OF PHARMACAL RESEARCH
Volume 31, Issue 1, Pages 96-102

Publisher

PHARMACEUTICAL SOC KOREA
DOI: 10.1007/s12272-008-1126-5

Keywords

nanoparticles; poly(L-lactic acid); polyethylenimine; transfection; non-viral gene delivery

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Non-viral vectors such as liposomes, polycations, and nanoparticles have been used as gene delivery systems. In this study, we prepared and characterized biodegradable poly(L-lactic acid) (PLA)/polyethylenimine (PEI) nanoparticles as gene carriers. pCMV/beta-gal and pEGFP-C1 were utilized as model plasmid DNAs (pDNA). Nanoparticles were prepared using a double emulsion-solvent evaporation technique, and their pDNA binding capacity was assessed by agarose gel electrophoresis. Transfection was studied in HEK 293 and HeLa cell lines, and the transfection efficiencies were determined by beta-galactosidase assay or flow cytometry. Three kinds of PLA/PEI systems were studied by varying the molecular weight of PEI. The PLA/PEl 25K system had a higher transfection efficiency than the PLA/PEI 0.8K or PLA/PEl 750K systems. The transfection efficiency was found to be dependent on the ratio of PLA/PEl nanoparticles to pDNA with an optimum ratio of 60:1 (w/w). The cytotoxicity was dependent on the quantity of PLA/PEl nanoparticles used, but it was comparable to that of commercial Lipofectin (TM). These results demonstrate the potential of PLA/PEI nanoparticles as gene carriers.

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