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Authors
Advisor(s)
Abstract(s)
Metal nanoparticles (M-NP) have application in several areas such as industry, environment,
agriculture, and biomedicine. Consequently, human exposure to these nanosized materials is
increasing, which raises serious concerns regarding their safety to the human health and the
environment. Biological barriers are important lines of defence to xenobiotics, thus expected
targets for M-NP. The present study investigated the in vitro toxicity of different types of M-NP
in two cell models of biological barriers: human intestinal (Caco-2) and trophoblastic (BeWo clone
b30) epithelial cells. Cells were exposed for 24 h to varied concentrations (0.8-48 µg/cm2) of M NP of different chemical composition (Au, Ag, TiO2), primary size (10, 30 and 60 nm), capping
(citrate, PEG) and crystal structure (rutile, anatase) and toxicity assessed by determining changes
in cell morphology, metabolic activity, plasma membrane integrity, generation of intracellular
reactive oxygen species (ROS) and intracellular ATP levels. Our data show that the potential
toxicity of the tested M-NPs is similar for both cell lines with AgNPs > AuNPs > TiO2NPs, being the
effects more visible at higher concentrations. The influence of the size in the cytotoxic-induced
effects was more evident for AgNP than for AuNP, with the smaller NP causing more toxicity,
being the BeWo cells more sensitive to these M-NP. In addition, PEG-capping effectively
attenuated AuNP-induced toxicity both in Caco-2 and BeWo cells. Only cells exposed to AgNP
exhibited significant increased levels of ROS. Thus, our data support that the physicochemical
properties of the nanomaterials, in this particular case of M-NP, is an important determinant of
their cytotoxicity and that intestinal and trophoblastic cells exhibit different sensitivity to the
tested M-NP. Future studies would be useful to further explore the effects of M-NP in the human
barriers
Description
Keywords
Metal Nanoparticles Genotoxicity Genotoxicidade Ambiental
