Open AccessUltraviolet radiation and nanoparticle induced intracellular free radicals generation measured in human keratinocytes by electron paramagnetic resonance spectroscopy
Author(s) -
Rancan F.,
Nazemi B.,
Rautenberg S.,
Ryll M.,
Hadam S.,
Gao Q.,
Hackbarth S.,
Haag S. F.,
Graf C.,
Rühl E.,
BlumePeytavi U.,
Lademann J.,
Vogt A.,
Meinke M. C.
Publication year - 2014
Publication title -
skin research and technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.521
H-Index - 69
eISSN - 1600-0846
pISSN - 0909-752X
DOI - 10.1111/srt.12104
Subject(s) - radical , nanoparticle , electron paramagnetic resonance , intracellular , photochemistry , chemistry , titanium dioxide , spectroscopy , biophysics , ultraviolet , materials science , nanotechnology , nuclear magnetic resonance , organic chemistry , biochemistry , optoelectronics , physics , quantum mechanics , metallurgy , biology
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.