Cytocompatibility and cellular internalization mechanisms of SiC/SiO 2 nanowires (Articolo in rivista)

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  • Cytocompatibility and cellular internalization mechanisms of SiC/SiO 2 nanowires (Articolo in rivista) (literal)
Anno
  • 2014-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1021/nl501255m (literal)
Alternative label
  • A. Cacchioli,1 F. Ravanetti,1 R. Alinovi,2 S. Pinelli,2 F. Rossi,3 M. Negri,3 E. Bedogni,4 M. Campanini,3 M. Galetti,5-6 M. Goldoni,2 P. Lagonegro,3 R. Alfieri,5 F. Bigi,4 and G. Salviati3 (2014)
    Cytocompatibility and cellular internalization mechanisms of SiC/SiO 2 nanowires
    in Nano letters (Print); American Chemical Society, Washington, DC (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • A. Cacchioli,1 F. Ravanetti,1 R. Alinovi,2 S. Pinelli,2 F. Rossi,3 M. Negri,3 E. Bedogni,4 M. Campanini,3 M. Galetti,5-6 M. Goldoni,2 P. Lagonegro,3 R. Alfieri,5 F. Bigi,4 and G. Salviati3 (literal)
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  • 4368 (literal)
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  • http://pubs.acs.org/doi/abs/10.1021/nl501255m (literal)
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  • 14 (literal)
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  • 1 Department of Veterinary Science, Unit of Normal Veterinary Anatomy, University of Parma, Parma 43126, Italy 2 Department of Clinical and Experimental Medicine, Laboratory of Industrial Toxicology, University of Parma, Parma 43126, Italy 3 IMEM-CNR Institute, Parco Area delle Scienze 37/A, Parma 43124, Italy 4 Department of Chemistry, University of Parma, Parma 43124, Italy 5 Department of Clinical and Experimental Medicine, Experimental Oncology Unit, University of Parma, Parma 43126, Italy 6 Italian Workers' Compensation Authority (INAIL) Research Center, Parma 43126, Italy (literal)
Titolo
  • Cytocompatibility and cellular internalization mechanisms of SiC/SiO 2 nanowires (literal)
Abstract
  • First evidence of in vitro cytocompatibility of SiC/SiO2 core-shell nanowires is reported. Different internalization mechanisms by adenocarcinomic alveolar basal epithelial cells, monocytic cell line derived from an acute monocytic leukemia, breast cancer cells, and normal human dermal fibroblasts are shown. The internalization occurs mainly for macropinocytosis and sporadically by direct penetration in all cell models considered, whereas it occurred for phagocytosis only in monocytic leukemia cells. The cytocompatibility of the nanowires is proved by the analysis of cell proliferation, cell cycle progression, and oxidative stress on the cells treated with NWs as compared to controls. Reactive oxygen species generation was detected as an early event that then quickly run out with a rapid decrease only in adenocarcinomic alveolar basal epithelial and human dermal fibroblasts cells. In all the cell lines, the intracellular presence of NWs induce the same molecular events but to a different extent: peroxidation of membrane lipids and oxidation of proteins. The NWs do not elicit either midterm (72 h) or long-term (10 days) cytotoxic activity leading to irreversible cellular damages or death. Our results are important in view of a possible use of SiC/SiO2 core-shell structures acting as biomolecule-delivery vectors or intracellular electrodes. (literal)
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