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Toxicol Appl Pharmacol ; 280(3): 484-92, 2014 Nov 01.
Article in English | MEDLINE | ID: mdl-25168427

ABSTRACT

Nanotechnology has been proven to be increasingly compatible with pharmacological and biomedical applications. Therefore, we evaluated the biological interactions of single-wall carbon nanotubes functionalized with polyethylene glycol (SWNT-PEG). For this purpose, we analyzed biochemical, histological, behavioral and biodistribution parameters to understand how this material behaves in vitro and in vivo using the fish Danio rerio (zebrafish) as a biological model. The in vitro results for fish brain homogenates indicated that SWNT-PEG had an effect on lipid peroxidation and GSH (reduced glutathione) content. However, after intraperitoneal exposure, SWNT-PEG proved to be less biocompatible and formed aggregates, suggesting that the PEG used for the nanoparticle functionalization was of an inappropriate size for maintaining product stability in a biological environment. This problem with functionalization may have contributed to the low or practically absent biodistribution of SWNT-PEG in zebrafish tissues, as verified by Raman spectroscopy. There was an accumulation of material in the abdominal cavity that led to inflammation and behavioral disturbances, as evaluated by a histological analysis and an open field test, respectively. These results provide evidence of a lack of biocompatibility of SWNTs modified with short chain PEGs, which leads to the accumulation of the material, tissue damage and behavioral alterations in the tested subjects.


Subject(s)
Brain/metabolism , Nanotubes, Carbon/toxicity , Polyethylene Glycols/pharmacology , Zebrafish/metabolism , Animals , Behavior, Animal/drug effects , Glutathione/analysis , Histocytochemistry , Male , Microscopy, Electron, Transmission , Nanotubes, Carbon/ultrastructure , Spectrum Analysis, Raman , Thiobarbituric Acid Reactive Substances/analysis , Tissue Distribution/physiology
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