Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/327757
Type: Artigo
Title: Reduced Graphene Oxide: Nanotoxicological Profile In Rats
Author: Padilha Mendonca
Monique Culturato; Soares
Edilene Siqueira; de Jesus
Marcelo Bispo; Ceragioli
Helder Jose; Irazusta
Silvia Pierre; Batista
Angela Giovana; Ramirez Vinolo
Marco Aurelio; Marostica Junior
Mario Roberto; da Cruz-Hofling
Maria Alice
Abstract: We have previously demonstrated that reduced graphene oxide (rGO) administered intravenously in rats was detected inside the hippocampus after downregulation of the tight and adherens junction proteins of the blood-brain barrier. While down-regulators of junctional proteins could be useful tools for drug delivery through the paracellular pathway, concerns over toxicity must be investigated before clinical application. Herein, our purpose was to trace whether the rGO inside the hippocampus triggered toxic alterations in this brain region and in target organs (blood, liver and kidney) of rats at various time points (15 min, 1, 3 h and 7 days). Results: The assessed rGO-treated rats (7 mg/kg) were clinically indistinguishable from controls at all the time points. Hematological, histopathological (neurons and astrocytes markers), biochemical (nephrotoxicity and hepatotoxicity assessment) and genotoxicological based tests showed that systemic rGO single injection seemed to produce minimal toxicological effects at the time points assessed. Relative to control, the only change was a decrease in the blood urea nitrogen level 3 h post-treatment and increases in superoxide dismutase activity 1 h and 7 days post-treatment. While no alteration in leukocyte parameters was detected between control and rGO-treated animals, time-dependent leukocytosis (rGO-1 h versus rGO-3 h) and leukopenia (rGO-3 h versus rGO-7 days) was observed intra-treated groups. Nevertheless, no inflammatory response was induced in serum and hippocampus at any time. Conclusions: The toxic effects seemed to be peripheral and transitory in the short-term analysis after systemic administration of rGO. The effects were self-limited and non-significant even at 7 days post-rGO administration.
Subject: Nanoparticles
Blood-brain Barrier
Toxicity
Editor: Biomed Central Ltd
London
Rights: aberto
Identifier DOI: 10.1186/s12951-016-0206-9
Address: https://jnanobiotechnology.biomedcentral.com.ez88.periodicos.capes.gov.br/articles/10.1186/s12951-016-0206-9
Date Issue: 2016
Appears in Collections:Unicamp - Artigos e Outros Documentos

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