dc.creatorDavid Gara, Pedro Maximiliano
dc.creatorGarabano, Natalia Ines
dc.creatorLlansola Portolés, Manuel Jose
dc.creatorMoreno, Mario Sergio Jesus
dc.creatorDodat, Diego
dc.creatorCasas, Oscar R.
dc.creatorGonzalez, Monica Cristina
dc.creatorKotler, Monica Lidia
dc.date.accessioned2018-09-24T17:55:40Z
dc.date.available2018-09-24T17:55:40Z
dc.date.created2018-09-24T17:55:40Z
dc.date.issued2012-04
dc.identifierDavid Gara, Pedro Maximiliano; Garabano, Natalia Ines; Llansola Portolés, Manuel Jose; Moreno, Mario Sergio Jesus; Dodat, Diego; et al.; ROS enhancement by silicon nanoparticles in X-ray irradiated aqueous suspensions and in glioma C6 cells; Springer; Journal of Nanoparticle Research; 14; 3; 4-2012; 741-754
dc.identifier1388-0764
dc.identifierhttp://hdl.handle.net/11336/60766
dc.identifierCONICET Digital
dc.identifierCONICET
dc.description.abstractThe capability of silicon nanoparticles to increase the yield of reactive species upon 4 MeV X-ray irradiation of aqueous suspensions and C6 glioma cell cultures was investigated. ROS generation was detected and quantified using several specific probes. The particles were characterized by FTIR, XPS, TEM, DLS, luminescence, and adsorption spectroscopy before and after irradiation to evaluate the effect of high energy radiation on their structure. The total concentration of O 2 ·-/HO 2 ·, HO ·, and H 2O 2 generated upon 4-MeV X-ray irradiation of 6.4 μM silicon nanoparticle aqueous suspensions were on the order of 10 μM per Gy, ten times higher than that obtained in similar experiments but in the absence of particles. Cytotoxic 1O 2 was generated only in irradiation experiments containing the particles. The particle surface became oxidized to SiO 2 and the luminescence yield reduced with the irradiation dose. Changes in the surface morphology did not affect, within the experimental error, the yields ofROSgenerated per Gy. X-ray irradiation of glioma C6 cell cultures with incorporated silicon nanoparticles showed a marked production of ROS proportional to the radiation dose received. In the absence of nanoparticles, the cells showed no irradiation- enhanced ROS generation. The obtained results indicate that silicon nanoparticles of <5 nm size have the potential to be used as radiosensitizers for improving the outcomes of cancer radiotherapy. Their capability of producing 1O 2 upon X-ray irradiation opens novel approaches in the design of therapy strategies. © Springer Science+Business Media B.V. 2012.
dc.languageeng
dc.publisherSpringer
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1007/s11051-012-0741-8
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007s11051-012-0741-8
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectGLIOMA C6 CELLS
dc.subjectRADIOTHERAPY
dc.subjectROS
dc.subjectSILICON NANOPARTICLES
dc.subjectSINGLET MOLECULAR OXYGEN
dc.subjectX-RAYS
dc.titleROS enhancement by silicon nanoparticles in X-ray irradiated aqueous suspensions and in glioma C6 cells
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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