Carbon nanoparticles for gene transfection In eukaryotic cell lines
H. Zanin, L.M. Hollanda, H.J. Ceragioli, M.S. Ferreira, D. Machado, M. Lancellotti R.R. Catharino, V. Baranauskas, A.O. Lobo
ARTIGO
Inglês
Agradecimentos: The authors would like to thank Brazilians agencies CNPq (202439/2012-7); CAPES and FAPESP (2011/17195-3) and (2011/17877-7) for financial support. Our sincere acknowledgements to Dr. Elaine Minatel, who helped us with the fluorescence images. The electron microscopy work was...
Ver mais
Agradecimentos: The authors would like to thank Brazilians agencies CNPq (202439/2012-7); CAPES and FAPESP (2011/17195-3) and (2011/17877-7) for financial support. Our sincere acknowledgements to Dr. Elaine Minatel, who helped us with the fluorescence images. The electron microscopy work was performed with a HRSEM (FEI-Inspect) microscope at the LME/LNLS-Campinas
Ver menos
For the first time, oxygen terminated cellulose carbon nanoparticles (CCN) was synthesised and applied in gene transfection of pIRES plasmid. The CCN was prepared from catalytic of polyaniline by chemical vapour deposition techniques. This plasmid contains one gene that encodes the green fluorescent...
Ver mais
For the first time, oxygen terminated cellulose carbon nanoparticles (CCN) was synthesised and applied in gene transfection of pIRES plasmid. The CCN was prepared from catalytic of polyaniline by chemical vapour deposition techniques. This plasmid contains one gene that encodes the green fluorescent protein (GFP) in eukaryotic cells, making them fluorescent. This new nanomaterial and pIRES plasmid formed π-stacking when dispersed in water by magnetic stirring. The frequencies shift in zeta potential confirmed the plasmid strongly connects to the nanomaterial. In vitro tests found that this conjugation was phagocytised by NG97, NIH-3T3 and A549 cell lines making them fluorescent, which was visualised by fluorescent microscopy. Before the transfection test, we studied CCN in cell viability. Both MTT and Neutral Red uptake tests were carried out using NG97, NIH-3T3 and A549 cell lines. Further, we use metabolomics to verify if small amounts of nanomaterial would be enough to cause some cellular damage in NG97 cells. We showed two mechanisms of action by CCN-DNA complex, producing an exogenous protein by the transfected cell and metabolomic changes that contributed by better understanding of glioblastoma, being the major finding of this work. Our results suggested that this nanomaterial has great potential as a gene carrier agent in non-viral based therapy, with low cytotoxicity, good transfection efficiency, and low cell damage in small amounts of nanomaterials in metabolomic tests
Ver menos
CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO - CNPQ
202439/2012-7
FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESP
2011/17195-3; 2011/17877-7
COORDENAÇÃO DE APERFEIÇOAMENTO DE PESSOAL DE NÍVEL SUPERIOR - CAPES
Fechado
Carbon nanoparticles for gene transfection In eukaryotic cell lines
H. Zanin, L.M. Hollanda, H.J. Ceragioli, M.S. Ferreira, D. Machado, M. Lancellotti R.R. Catharino, V. Baranauskas, A.O. Lobo
Carbon nanoparticles for gene transfection In eukaryotic cell lines
H. Zanin, L.M. Hollanda, H.J. Ceragioli, M.S. Ferreira, D. Machado, M. Lancellotti R.R. Catharino, V. Baranauskas, A.O. Lobo
Fontes
|
Materials science and engineering C: materials for biological applications (Fonte avulsa) |