Serum proteins prevent aggregation of Fe2O3 and ZnO nanoparticles

被引:73
|
作者
Wells, Mark A. [1 ]
Abid, Aamir [1 ]
Kennedy, Ian M. [1 ]
Barakat, Abdul I. [1 ,2 ]
机构
[1] Univ Calif Davis, Dept Mech & Aerosp Engn, Davis, CA 95616 USA
[2] Ecole Polytech, Hydrodynam Lab LadHyX, CNRS UMR7646, F-91128 Palaiseau, France
基金
美国国家环境保护局;
关键词
Metal oxide nanoparticles; particle aggregation; particle aging; dynamic light scattering; zeta potential; fluid shear; METAL-OXIDE NANOPARTICLES; TIO2; NANOPARTICLES; ADSORPTION; PARTICLES; FIBRILLATION; MACROPHAGES; EXPOSURE; PH;
D O I
10.3109/17435390.2011.625131
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Aggregation of metal oxide nanoparticles in aqueous media complicates interpretation of in vitro studies of nanoparticle-cell interactions. We used dynamic light scattering to investigate the aggregation dynamics of iron oxide and zinc oxide nanoparticles. Our results show that iron oxide particles aggregate more readily than zinc oxide particles. Pretreatment with serum stabilises iron oxide and zinc oxide nanoparticles against aggregation. Serum-treated iron oxide is stable only in pure water, while zinc oxide is stable in water or cell culture media. These findings, combined with zeta potential measurements and quantification of proteins adsorbed on particle surface, suggest that serum stabilisation of iron oxide particles occurs primarily through protein adsorption and resulting net surface charge. Zinc oxide stabilisation, however, also involves steric hindrance of particle aggregation. Fluid shear at levels used in flow experiments breaks up iron oxide particle aggregates. These results enhance our understanding of nanoparticle aggregation and its consequences for research on the biological effects of nanomaterials.
引用
收藏
页码:837 / 846
页数:10
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