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J Phys Chem B ; 117(6): 1550-5, 2013 Feb 14.
Article in English | MEDLINE | ID: mdl-22746541

ABSTRACT

The transfer of genetic information into living cells is a powerful tool to manipulate their protein expression by the regulation of protein synthesis. This can be used for the treatment of genetically caused diseases (gene therapy). However, the systemic application of genes is associated with a number of problems, such as a targeted gene delivery and potential side effects. Here we present a method for the spatial application of nanoparticle-based gene therapy. Titanium was electrophoretically coated with DNA-functionalized calcium phosphate nanoparticles. NIH3T3 cells and HeLa cells were transfected with pcDNA3-EGFP. We monitored the transfection in vitro by fluorescence microscopy, flow cytometry, and Western Blot analysis. By coating a transparent substrate, i.e., indium tin oxide (ITO), with nanoparticles, we followed the transfection by live cell imaging.


Subject(s)
Metals/chemistry , Nanoparticles/chemistry , Animals , Gene Transfer Techniques , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , HeLa Cells , Humans , Mice , Microscopy, Fluorescence , NIH 3T3 Cells , Plasmids/genetics , Plasmids/metabolism , Surface Properties , Tin Compounds/chemistry , Transfection
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