Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/327905
Type: Artigo
Title: Pegylation Of Reduced Graphene Oxide Induces Toxicity In Cells Of The Blood-brain Barrier: An In Vitro And In Vivo Study
Author: Padilha Mendonca
Monique Culturato; Soares
Edilene Siqueira; de Jesus
Marcelo Bispo; Ceragioli
Helder Jose; Batista
Angela Giovana; Nyul-Toth
Adam; Molnar
Judit; Wilhelm
Imola; Marostica
Mario Roberto
Jr.; Krizbai
Istvan; da Cruz-Hofling
Maria Alice
Abstract: Polyethylene glycol (PEG) coating has been frequently used to improve the pharmacokinetic behavior of nanoparticles. Studies that contribute to better unravel the effects of PEGylation on the toxicity of nanoparticle formulation are therefore highly relevant. In the present study, reduced graphene oxide (rGO) was functionalized with PEG, and its effects on key components of the blood-brain barrier, such as astrocytes and endothelial cells, were analyzed in culture and in an in vivo rat model. The in vitro studies demonstrated concentration-dependent toxicity. The highest concentration (100 mu g/mL) of non-PEGylated rGO had a lower toxic influence on cell viability in primary cultures of astrocytes and rat brain endothelial cells, while PEGylated rGO induced deleterious effects and cell death. We assessed hippocampal BBB integrity in vivo by evaluating astrocyte activation and the expression of the endothelial tight and adherens junctions proteins. From 1 h to 7 days post-rGO-PEG systemic injection, a notable and progressive down-regulation of protein markers of astrocytes (GFAP, connexin-43), the endothelial tight (occludin), and adherens (beta-catenin) junctions and basal lamina (laminin) were observed. The formation of intracellular reactive oxygen species demonstrated by increases in the enzymatic antioxidant system in the PEGylated rGO samples was indicative of oxidative stress-mediated damage. Under the experimental conditions and design of the present study the PEGylation of rGO did not improve interaction with components of the blood brain barrier. In contrast, the attachment of PEG to rGO induced deleterious effects in comparison with the effects caused by non-PEGylated rGO.
Subject: Pegylation
Graphene-based Nanomaterials
Central Nervous System
Nanotoxicity
Editor: Amer Chemical Soc
Washington
Citation: Molecular Pharmaceutics. Amer Chemical Soc, v. 13, p. 3913 - 3924, 2016.
Rights: fechado
Identifier DOI: 10.1021/acs.molpharmaceut.6b00696
Address: http://www.annualreviews.org/doi/full/10.1146/annurev-arplant-043014-114648?url_ver=Z39.88-2003&rfr_id=ori%3Arid%3Acrossref.org&rfr_dat=cr_pub%3Dpubmed
Date Issue: 2016
Appears in Collections:Unicamp - Artigos e Outros Documentos

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