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Toxicita magnetických nanočástic
[Toxicity of magnetic nanoparticles]
Lucie Kučírková, Karel Královec, Radim Havelek, Lenka Brůčková, Miloš Sedlák
Language Czech Country Czech Republic
Document type Research Support, Non-U.S. Gov't
- Keywords
- MNPs, SPIONs,
- MeSH
- Metal Nanoparticles chemistry adverse effects therapeutic use toxicity MeSH
- Humans MeSH
- Magnetite Nanoparticles * chemistry adverse effects therapeutic use toxicity MeSH
- Oxidative Stress MeSH
- In Vitro Techniques MeSH
- Toxicity Tests * MeSH
- Cell Survival MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Research Support, Non-U.S. Gov't MeSH
In recent years, Fe oxide nanoparticles have been increasingly used in a wide range of biomedical applications, including magnetic resonance imaging, magnetic hyperthermia, targeted drug and gene delivery, cell tracking and magnetic cell separation. Although the number of studies examining the toxicity of Fe oxide nanoparticles is growing exponentially, the in-depth toxicity studies are scanty and the mechanisms underlying their cytotoxicity remain still mostly unclear. This review focuses on the assessment of the in vitro and in vivo toxicity of Fe oxide nanoparticles and discusses the biological processes underlying their toxicity including cellular uptake, production of reactive O species, modulation of actin and microtubular cytoskeleton, DNA damage and activation of intracellular signalling pathways. The significance of the proteins associated with Fe oxide nanoparticles and assays for assessing their cytotoxicity are also considered. We have tested cytotoxic effects of silica-coated Fe oxide nanoparticles on human lung adenocarcinoma, epithelial cell line A549 using the xCELLigence system for label-free and real-time monitoring of cell viability.
Toxicity of magnetic nanoparticles
Literatura
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- $a In recent years, Fe oxide nanoparticles have been increasingly used in a wide range of biomedical applications, including magnetic resonance imaging, magnetic hyperthermia, targeted drug and gene delivery, cell tracking and magnetic cell separation. Although the number of studies examining the toxicity of Fe oxide nanoparticles is growing exponentially, the in-depth toxicity studies are scanty and the mechanisms underlying their cytotoxicity remain still mostly unclear. This review focuses on the assessment of the in vitro and in vivo toxicity of Fe oxide nanoparticles and discusses the biological processes underlying their toxicity including cellular uptake, production of reactive O species, modulation of actin and microtubular cytoskeleton, DNA damage and activation of intracellular signalling pathways. The significance of the proteins associated with Fe oxide nanoparticles and assays for assessing their cytotoxicity are also considered. We have tested cytotoxic effects of silica-coated Fe oxide nanoparticles on human lung adenocarcinoma, epithelial cell line A549 using the xCELLigence system for label-free and real-time monitoring of cell viability.
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