Low toxicity and accumulation of zinc oxide nanoparticles in mice after 270-day consecutive dietary supplementation.

Toxicol Res (Camb)

Beijing National Laboratory for Molecular Sciences , College of Chemistry and Molecular Engineering , Peking University, Beijing 100871 , China . Email:

Published: March 2017

The toxicity and accumulation of zinc oxide nanoparticles (ZnO-NPs), ZnO microparticles (ZnO-MPs) and Zn ions were evaluated after long-term feeding with zinc-replenished food (1600 mg zinc equivalent per kg food) for 270 consecutive days. It was difficult for ZnO-NPs, ZnO-MPs and Zn ions were difficult to pass through the intestine barrier, and most of them were excreted mainly through feces. The distribution results showed that there was no noticeable difference among the distribution profiles of ZnO-NPs, ZnO-MPs and Zn ions in mice. Zn accumulated only in the digestive tract organs after the exposure to all three samples. However, the biomedical parameters and pathological investigations showed liver lesions induced by ZnO-MPs, but fewer by ZnO-NPs or Zn ions. The reason for the remarkably low toxicity of ZnO-NPs is discussed. Our findings suggest that ZnO-NPs are relatively biocompatible as the nutritional additive at the commonly used dose.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6062400PMC
http://dx.doi.org/10.1039/c6tx00370bDOI Listing

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Low toxicity and accumulation of zinc oxide nanoparticles in mice after 270-day consecutive dietary supplementation.

Toxicol Res (Camb)

March 2017

Beijing National Laboratory for Molecular Sciences , College of Chemistry and Molecular Engineering , Peking University, Beijing 100871 , China . Email:

The toxicity and accumulation of zinc oxide nanoparticles (ZnO-NPs), ZnO microparticles (ZnO-MPs) and Zn ions were evaluated after long-term feeding with zinc-replenished food (1600 mg zinc equivalent per kg food) for 270 consecutive days. It was difficult for ZnO-NPs, ZnO-MPs and Zn ions were difficult to pass through the intestine barrier, and most of them were excreted mainly through feces. The distribution results showed that there was no noticeable difference among the distribution profiles of ZnO-NPs, ZnO-MPs and Zn ions in mice.

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Abstract Understanding tissue biodistribution and clearance of zinc oxide nanoparticles (ZnO-NPs) is necessary for its risk assessment. Both fed and intraperitoneally injected ZnO-NPs (2.5 g/kg) were absorbed into circulation (within 30 min post-dosing), then biodistributed to the liver, spleen, and kidney.

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