Toxicity of surface-modified copper oxide nanoparticles in a mouse macrophage cell line: Interplay of particles, surface coating and particle dissolution
Language English Country England, Great Britain Media print-electronic
Document type Journal Article
PubMed
29324388
DOI
10.1016/j.chemosphere.2017.12.182
PII: S0045-6535(17)32160-4
Knihovny.cz E-resources
- Keywords
- Cytotoxicity, Macrophages, Nanoparticles, Oxidative stress, Surface coating,
- MeSH
- Antioxidants MeSH
- Cell Death drug effects MeSH
- Cell Line MeSH
- Metal Nanoparticles chemistry toxicity MeSH
- Macrophages metabolism MeSH
- Copper chemistry pharmacokinetics toxicity MeSH
- Mice MeSH
- Surface Properties MeSH
- Reactive Oxygen Species metabolism MeSH
- Solubility MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antioxidants MeSH
- cuprous oxide MeSH Browser
- Copper MeSH
- Reactive Oxygen Species MeSH
The rapid dissolution of copper oxide (CuO) nanoparticles (NPs) with release of ions is thought to be one of the main factors modulating their toxicity. Here we assessed the cytotoxicity of a panel of CuO NPs (12 nm ± 4 nm) with different surface modifications, i.e., anionic sodium citrate (CIT) and sodium ascorbate (ASC), neutral polyvinylpyrrolidone (PVP), and cationic polyethylenimine (PEI), versus the pristine (uncoated) NPs, using a murine macrophage cell line (RAW264.7). Cytotoxicity, reactive oxygen species (ROS) production, and cellular uptake were assessed. The cytotoxicity results were analyzed by the benchmark dose (BMD) method and the NPs were ranked based on BMD20 values. The PEI-coated NPs were found to be the most cytotoxic. Despite the different properties of the coating agents, NP dissolution in cell medium was only marginally affected by surface modification. Furthermore, CuCl2 (used as an ion control) elicited significantly less cytotoxicity when compared to the CuO NPs. We also observed that the antioxidant, N-acetylcysteine, failed to protect against the cytotoxicity of the uncoated CuO NPs. Indeed, the toxicity of the surface-modified CuO NPs was not directly linked to particle dissolution and subsequent Cu burden in cells, nor to cellular ROS production, although CuO-ASC NPs, which were found to be the least cytotoxic, yielded lower levels of ROS in comparison to pristine NPs. Hierarchical cluster analysis suggested, instead, that the toxicity in the current in vitro model could be explained by synergistic interactions between the NPs, their dissolution, and the toxicity of the coating agents.
Institute of Experimental Medicine Academy of Sciences of the Czech Republic Prague Czech Republic
Institute of Science and Technology for Ceramics National Research Council of Italy Faenza Italy
References provided by Crossref.org
The negative effect of magnetic nanoparticles with ascorbic acid on peritoneal macrophages
