Acute toxicity and biodistribution of different sized titanium dioxide particles in mice after oral administration

Wang, JX; Zhou, GQ; Chen, CY; Yu, HW; Wang, TC; Ma, YM; Jia, G; Gao, YX; Li, B; Sun, J; Li, YF; Jiao, F; Zhao, YL; Chai, ZF

HERO ID

90290

Reference Type

Journal Article

Year

2007

Language

English

PMID

17197136

HERO ID 90290
In Press No
Year 2007
Title Acute toxicity and biodistribution of different sized titanium dioxide particles in mice after oral administration
Authors Wang, JX; Zhou, GQ; Chen, CY; Yu, HW; Wang, TC; Ma, YM; Jia, G; Gao, YX; Li, B; Sun, J; Li, YF; Jiao, F; Zhao, YL; Chai, ZF
Journal Toxicology Letters
Volume 168
Issue 2
Page Numbers 176-185
Abstract In order to evaluate the toxicity of TiO2 particles, the acute toxicity of nano-sized TiO2 particles (25 and 80 nm) on adult mice was investigated compared with fine TiO2 particles (155 nm). Due to the low toxicity, a fixed large dose of 5 g/kg body weight of TiO2 suspensions was administrated by a single oral gavage according to the OECD procedure. In 2 weeks, TiO2 particles showed no obvious acute toxicity. However, the female mice showed high coefficients of liver in the nano-sized (25 and 80 nm) groups. The changes of serum biochemical parameters (ALT/AST, LDH) and pathology (hydropic degeneration around the central vein and the spotty necrosis of hepatocytes) of liver indicated that the hepatic injury was induced after exposure to mass different-sized TiO2 particles. In addition, the nephrotoxicity like increased BUN level and pathology change of kidneys was also observed in the experimental groups. The significant change of serum LDH and alpha-HBDH in 25 and 80 nm groups showed the myocardial damage compared with the control group. However, there are no abnormal pathology changes in the heart, lung, testicle (ovary), and spleen tissues. Biodistribution experiment showed that TiO2 mainly retained in the liver, spleen, kidneys, and lung tissues, which indicated that TiO2 particles could be transported to other tissues and organs after uptake by gastrointestinal tract.
Doi 10.1016/j.toxlet.2006.12.001
Pmid 17197136
Wosid WOS:000244059300010
Is Certified Translation No
Dupe Override No
Comments ECRIB.Toxicol. Lett. 168: 176-185.
Is Public Yes
Language Text English
Keyword acute toxicity; fixed dose procedure; titanium dioxide; nanoparticles; mice
Is Qa No
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