In vitro toxicity of nanoceria: effect of coating and stability in biofluids

被引:44
|
作者
Ould-Moussa, Nawel [1 ]
Safi, Malak [1 ]
Guedeau-Boudeville, Marie-Alice [1 ]
Montero, David [2 ]
Conjeaud, Helene [1 ]
Berret, Jean-Francois [1 ]
机构
[1] Univ Paris 07, UMR CNRS 7057, F-75205 Paris, France
[2] Univ Paris 06, FR CNRS 2482, Inst Mat Paris Ctr, Paris, France
关键词
nanoparticles; interfaces; cells; spectrometry; toxicity; CERIUM OXIDE NANOPARTICLES; VASCULAR ENDOTHELIAL-CELLS; OXIDATIVE STRESS; ENGINEERED NANOMATERIAL; CEO2; NANOPARTICLES; DIOXIDE NANOPARTICLES; CELLULAR-RESPONSES; EPITHELIAL-CELLS; MAMMALIAN-CELLS; CYTOTOXICITY;
D O I
10.3109/17435390.2013.831501
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Due to the increasing use of nanometric cerium oxide in applications, concerns about the toxicity of these particles have been raised and have resulted in a large number of studies. We report here on the interactions between 7 nm anionically charged cerium oxide particles and living mammalian cells. By a modification of the particle coating including low-molecular weight ligands and polymers, two generic behaviours are compared: particles coated with citrate ions that precipitate in biofluids and particles coated with poly(acrylic acid) that are stable and remain nanometric. We find that nanoceria covered with both coating agents are taken up by mouse fibroblasts and localized into membrane-bound compartments. However, flow cytometry and electron microscopy reveal that as a result of their precipitation, citrate-coated particles interact more strongly with cells. At cerium concentration above 1 mM, only citratecoated nanoceria (and not particles coated with poly(acrylic acid)) display toxicity and moderate genotoxicity. The results demonstrate that the control of the surface chemistry of the particles and its ability to prevent aggregation can affect the toxicity of nanomaterials.
引用
收藏
页码:799 / 811
页数:13
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