Affiliation:
1. School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, P. R. China
2. National Engineering Research Center for Nanotechnology, Shanghai 200241, P. R. China
Abstract
In recent years, with the widespread use of zinc oxide (ZnO) nanoparticles (NPs), more and more attentions are being given to its biological toxicity, the toxicity of ZnO NPs under different exposure methods is necessary to investigate. In this study, we prepared two ZnO dispersions
with different particle sizes, namely small-size ZnO (S-ZnO) and Bigsize ZnO (B-ZnO), using polycarboxylic acid as dispersant. Mice were poisoned by intravenous injection and inhalation, respectively. The respiration coefficient, superoxide dismutase (SOD), Zn content in the organs of the
mice were detected. It was discovered that ZnO NPs with smaller particle diameter can cause more serious toxicity in vivo after intravenous exposure and respiratory exposure. In addition, the mice showed symptoms of dyspnea after respiratory exposure and a massive number of fibroblasts
were found in the alveolar structure of the lungs. In the intravenous injection group, the content of Zn in the liver and spleen of mice increased significantly, resulting in organ edema, and the organ coefficient of mice increased. Finally, the increase of GSH/GSSG indicated that cells were
regulated under the antioxidant mechanism, which accelerated the removal of H2O2 from cells. In addition, the increase of GSH+GSSG content also indicated that ZnO NPs stimulated the creation of reactive oxygen species (ROS) in organs of experimental animals.
Publisher
American Scientific Publishers
Subject
Pharmaceutical Science,General Materials Science,Biomedical Engineering,Medicine (miscellaneous),Bioengineering
Cited by
1 articles.
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