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Titanium dioxide nanoparticles oral exposure to pregnant rats and its distribution

BACKGROUND: Titanium dioxide (TiO(2)) nanoparticles are among the most manufactured nanomaterials in the industry, and are used in food products, toothpastes, cosmetics and paints. Pregnant women as well as their conceptuses may be exposed to TiO(2) nanoparticles; however, the potential effects of t...

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Detalles Bibliográficos
Autores principales: Lee, Jinsoo, Jeong, Ji-Seong, Kim, Sang Yun, Park, Min-Kyu, Choi, Sung-Deuk, Kim, Un-Jung, Park, Kwangsik, Jeong, Eun Ju, Nam, Sang-Yoon, Yu, Wook-Joon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639912/
https://www.ncbi.nlm.nih.gov/pubmed/31319864
http://dx.doi.org/10.1186/s12989-019-0313-5
Descripción
Sumario:BACKGROUND: Titanium dioxide (TiO(2)) nanoparticles are among the most manufactured nanomaterials in the industry, and are used in food products, toothpastes, cosmetics and paints. Pregnant women as well as their conceptuses may be exposed to TiO(2) nanoparticles; however, the potential effects of these nanoparticles during pregnancy are controversial, and their internal distribution has not been investigated. Therefore, in this study, we investigated the potential effects of oral exposure to TiO(2) nanoparticles and their distribution during pregnancy. TiO(2) nanoparticles were orally administered to pregnant Sprague-Dawley rats (12 females per group) from gestation days (GDs) 6 to 19 at dosage levels of 0, 100, 300 and 1000 mg/kg/day, and then cesarean sections were conducted on GD 20. RESULTS: In the maternal and embryo-fetal examinations, there were no marked toxicities in terms of general clinical signs, body weight, food consumption, organ weights, macroscopic findings, cesarean section parameters and fetal morphological examinations. In the distribution analysis, titanium contents were increased in the maternal liver, maternal brain and placenta after exposure to high doses of TiO(2) nanoparticles. CONCLUSION: Oral exposure to TiO(2) during pregnancy increased the titanium concentrations in the maternal liver, maternal brain and placenta, but these levels did not induce marked toxicities in maternal animals or affect embryo-fetal development. These results could be used to evaluate the human risk assessment of TiO(2) nanoparticle oral exposure during pregnancy, and additional comprehensive toxicity studies are deemed necessary considering the possibility of complex exposure scenarios and the various sizes of TiO(2) nanoparticles.