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Long-term exposure to commercially available sunscreens containing nanoparticles of TiO(2) and ZnO revealed no biological impact in a hairless mouse model

BACKGROUND: The application of sunscreen is a critical component of a sun-safe strategy, however the possibility of unexpected, adverse outcomes resulting from long-term use of sunscreens containing nanoparticles of titanium dioxide (TiO(2)) and zinc oxide (ZnO) has not yet been examined. Here, immu...

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Detalles Bibliográficos
Autores principales: Osmond-McLeod, Megan J., Oytam, Yalchin, Rowe, Anthony, Sobhanmanesh, Fariborz, Greenoak, Gavin, Kirby, Jason, McInnes, Elizabeth F., McCall, Maxine J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989375/
https://www.ncbi.nlm.nih.gov/pubmed/27534937
http://dx.doi.org/10.1186/s12989-016-0154-4
Descripción
Sumario:BACKGROUND: The application of sunscreen is a critical component of a sun-safe strategy, however the possibility of unexpected, adverse outcomes resulting from long-term use of sunscreens containing nanoparticles of titanium dioxide (TiO(2)) and zinc oxide (ZnO) has not yet been examined. Here, immune-competent hairless mice were exposed over a 36-week period to weekly topical applications of sunscreens containing nanoparticles of ZnO or TiO(2), or no metal oxide nanoparticles, with or without subsequent exposure to ultraviolet radiation (UVR). Control groups received no sunscreen applications, with or without UVR. RESULTS: Mice exposed to UVR in the absence of sunscreen developed statistically significant incidences of histologically-diagnosed malignant and benign skin neoplasms, whereas no statistically significant adverse biological outcomes were found in mice treated with the sunscreens containing ZnO or TiO(2) nanoparticles. Elevated levels of Ti were detected in the livers of mice treated with sunscreen containing TiO(2) nanoparticles compared to untreated control, but total Zn concentrations did not significantly alter in any major organs except for the skin of mice treated with ZnO sunscreen. Exposure to UVR did not have a significant impact on examined tissue concentrations of Zn or Ti. Few to no transcriptional changes were found in ZnO or TiO(2)-treated groups, but mice treated with the sunscreen containing only organic filters showed substantial gene disregulation. CONCLUSIONS: Taken together with previous work, this long-term study provided no basis to avoid the use of sunscreens containing metal oxide nanoparticles.