Journal of Biomaterials Applications · 2012 · 16 citations · 32 references
PharmacyBioengineeringBiotechnologyAnimal BiotechnologyGene DeliveryMolecular BiotechnologyGene Delivery SystemsGene Delivery VectorsIn Vivo Gene DeliveryNanomaterials For Drug DeliveryNucleic Acid DeliveryPlasmid Dna DeliveryGelatin NanoparticlesGene Delivery CarriersGene Delivery NanocarriersGene Delivery NanoparticlesNanocarriersNanoparticlesNonviral Delivery SystemsNonviral Gene Delivery Vectors
To develop a safe and effective nonviral gene delivery system for transgenic chicken manipulation, we developed gelatin nanocarriers using a reporter plasmid (pEGFP-C1; enhanced green fluorescence protein, EGFP) that expressed EGFP. pEGFP-C1-containing gelatin nanoparticles (GP/pEGFP) were prepared using a water-ethanol solvent displacement method and characterized by size, surface charge, DNA loading, and DNA protection ability. For gene delivery, pEGFP-C1 was stably and efficiently encapsulated in GPs that were approximately 300 nm in diameter with a slight negative surface charge, which was prepared from gelatin solution at pH 8.0. Approximately, 85% of the plasmid DNA was encapsulated in the GPs. Electrophoresis results showed that the GPs provided protection against DNase I digestion. We used the GP/pEGFP as a vector to transfect cells and chicken embryos. The vector was nontoxic to cells, and GFP expression was effectively expressed 24 h after HeLa cell transfection. Direct injection was adapted for vector transport to the chicken embryo; injection in the area opaca (Ao) of the egg resulted in the highest hatching rate without affecting embryo development. GFP gene expression in embryo sections was observed 4 days after injection. The results of this study demonstrate that GPs are a suitable nonviral vector for delivering exogenous genes for transgenic chicken manipulation.
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