银纳米粒子
体内
毒性
化学
核化学
电感耦合等离子体质谱法
纳米颗粒
银染
纳米毒理学
脾脏
放射化学
色谱法
材料科学
内科学
分子生物学
生物
纳米技术
质谱法
医学
有机化学
生物技术
作者
Meike van der Zande,Rob J. Vandebriel,Elke Van Doren,Evelien Kramer,Zahira Herrera Rivera,Cecilia S. Serrano-Rojero,Eric R. Gremmer,Jan Mast,Ruud Peters,P.C.H. Hollman,Peter J.M. Hendriksen,H.J.P. Marvin,Ad Peijnenburg,Hans Bouwmeester
出处
期刊:ACS Nano
[American Chemical Society]
日期:2012-08-09
卷期号:6 (8): 7427-7442
被引量:600
摘要
We report the results of a 28-day oral exposure study in rats, exposed to <20 nm noncoated, or <15 nm PVP-coated silver nanoparticles ([Ag] = 90 mg/kg body weight (bw)), or AgNO3 ([Ag] = 9 mg/kg bw), or carrier solution only. Dissection was performed at day 29, and after a wash-out period of 1 or 8 weeks. Silver was present in all examined organs with the highest levels in the liver and spleen for all silver treatments. Silver concentrations in the organs were highly correlated to the amount of Ag+ in the silver nanoparticle suspension, indicating that mainly Ag+, and to a much lesser extent silver nanoparticles, passed the intestines in the silver nanoparticle exposed rats. In all groups silver was cleared from most organs after 8 weeks postdosing, but remarkably not from the brain and testis. Using single particle inductively coupled plasma mass spectrometry, silver nanoparticles were detected in silver nanoparticle exposed rats, but, remarkably also in AgNO3 exposed rats, hereby demonstrating the formation of nanoparticles from Ag+in vivo that are probably composed of silver salts. Biochemical markers and antibody levels in blood, lymphocyte proliferation and cytokine release, and NK-cell activity did not reveal hepatotoxicity or immunotoxicity of the silver exposure. In conclusion, oral exposure to silver nanoparticles appears to be very similar to exposure to silver salts. However, the consequences of in vivo formation of silver nanoparticles, and of the long retention of silver in brain and testis should be considered in a risk assessment of silver nanoparticles.
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