Comparison of the Mechanism of Toxicity of Zinc Oxide and Cerium Oxide Nanoparticles Based on Dissolution and Oxidative Stress Properties
By Tian Xia, M. Kovochich, M. Liong, Lutz Mädler, B. Gilbert, Haibin Shi, Joanne I. Yeh, J. Zink, A. Nel. ACS Nano, 2008
2,383 citations recorded by the source corpus.
Nanomaterials (NM) exhibit novel physicochemical properties that determine their interaction with biological substrates and processes. Three metal oxides nanoparticles that are currently being produced in high tonnage, TiO2, ZnO and CeO2, were synthesized by flame spray pyrolysis process and compared in a mechanistic study to elucidate the physicochemical characteristics that determine cellular uptake, subcellular localization, and toxic effects based on a test paradigm that was originally developed for oxidative stress and cytotoxicity in RAW 264.7 and BEAS-2B cell lines. ZnO induced toxicity in both cells, leading to the generation of reactive oxygen species (ROS), oxidant injury, excitation of inflammation and cell death. Using ICP-MS and fluorescent-labeled ZnO, it is found that ZnO dissolution could happen in culture medium and endosomes. Non-dissolved ZnO nanoparticles enter caveolae in BEAS-2B, but enter lysosomes in RAW 264.7 cells in which smaller particle remnants dissolve. In contrast, fluorescent-labeled CeO2 nanoparticles were taken up intact into caveolin-1 and LAMP-1 positive endosomal compartments, respectively, in BEAS-2B and RAW 264.7 cells, without inflammation or cytotoxicity. Instead, CeO2 suppressed ROS production and induced cellular resistance to an exogenous source of oxidative stress. Fluorescent-labeled TiO2 was processed by the same uptake pathways as CeO2 but did not elicit any adverse or protective effects. These results demonstrate that metal oxide nanoparticles induce a range of biological responses that vary from cytotoxic to cytoprotective and can only be properly understood by using a tiered test strategy such as we developed for oxidative stress and adapted to study other aspects of nanoparticle toxicity.
Subfields: Materials Chemistry
View Paper: https://www.semanticscholar.org/paper/095bb288529644790c6b62a9d8c6499d5a0b65d5
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Materials Chemistry
Citations in the corpus
- Interaction of nanoparticles with proteins: relation to bio-reactivity of the nanoparticle (2013, background): “For detecting elemental composition of the nanomaterial [90]”
- The Toxic Effects and Mechanisms of CuO and ZnO Nanoparticles (2012, background): “abundance of ROS production, the type of cellular pathways, and the antioxidant response element that are engaged in oxidative stress [108].”
- Emerging patterns for engineered nanomaterials in the environment: a review of fate and toxicity studies (2014, background): “With the exception of ZnO in seawater (Fairbairn et al. 2011; Li et al. 2013; Miller et al. 2010; Xia et al. 2008) and freshwater (Franklin et al.”
- Interactions between nanoparticles and plants: phytotoxicity and defense mechanisms (2017, background): “Compared to high-solubility NPs such as ZnONPs and Ag NPs (Xia et al. 2008; Oukarroum et al. 2013), CeO2 NPs are generally regarded as stable regardless of the biological or environmental systems involved, which were always used as a model material to study the phytotoxicity mechanisms of NPs.”
- ZnO nanoparticles (ZnO-NPs) and their antifungal activity against coffee fungus Erythricium salmonicolor (2017, background): “Recent work indicates that the nanoparticles induce oxidative stress (Xia et al. 2008).”
- Polyethyleneimine coating enhances the cellular uptake of mesoporous silica nanoparticles and allows safe delivery of siRNA and DNA constructs. (2009, methodology): “To conduct biological experimentation, particle size and potential were measured in water as well as tissue culture media.(31) For the purposes of this study, we used DMEM supplemented with 10% fetal calf serum (FCS) or BEGM as is or supplemented with 2 mg/mL BSA (Table 1).”
- The Targeted Delivery of Multicomponent Cargos to Cancer Cells via Nanoporous Particle-Supported Lipid Bilayers (2011, background): “, and the composition of the SLB was optimized to reduce nonspecific binding associated with cationic and, to a lesser extent, anionic lipids”