1. Ultraviolet radiation and nanoparticle induced intracellular free radicals generation measured in human keratinocytes by electron paramagnetic resonance spectroscopy.
- Author
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Rancan F, Nazemi B, Rautenberg S, Ryll M, Hadam S, Gao Q, Hackbarth S, Haag SF, Graf C, Rühl E, Blume-Peytavi U, Lademann J, Vogt A, and Meinke MC
- Subjects
- Cell Line, Dose-Response Relationship, Drug, Dose-Response Relationship, Radiation, Humans, Keratinocytes drug effects, Keratinocytes radiation effects, Nanoparticles ultrastructure, Particle Size, Radiation Dosage, Electron Spin Resonance Spectroscopy methods, Free Radicals metabolism, Interleukin-6 metabolism, Keratinocytes metabolism, Nanoparticles toxicity, Silicon Dioxide toxicity, Ultraviolet Rays adverse effects
- Abstract
Background: Several nanoparticle-based formulations used in cosmetics and dermatology are exposed to sunlight once applied to the skin. Therefore, it is important to study possible synergistic effects of nanoparticles and ultraviolet radiation., Methods: Electron paramagnetic resonance spectroscopy (EPR) was used to detect intracellular free radicals induced by ultraviolet B (UVB) radiation and amorphous silica nanoparticle and to evaluate the influence of nanoparticle surface chemistry on particle cytotoxicity toward HaCaT cells. Uncoated titanium dioxide nanoparticles served as positive control. In addition, particle intracellular uptake, viability, and induction of interleukin-6 were measured., Results: We found that photo-activated titanium dioxide particles induced a significant amount of intracellular free radicals. On the contrary, no intracellular free radicals were generated by the investigated silica nanoparticles in the dark as well as under UVB radiation. However, under UVB exposure, the non-functionalized silica nanoparticles altered the release of IL-6. At the same concentrations, the amino-functionalized silica nanoparticles had no influence on UVB-induced IL-6 release., Conclusion: EPR spectroscopy is a useful technique to measure nanoparticle-induced intracellular free radicals. Non-toxic concentrations of silica particles enhanced the toxicity of UVB radiation. This synergistic effect was not mediated by particle-generated free radicals and correlated with particle surface charge and intracellular distribution., (© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
- Published
- 2014
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