Protein adsorption and cellular uptake of cerium oxide nanoparticles as a function of zeta potential

被引:852
作者
Patil, Swanand
Sandberg, Amanda
Heckert, Eric
Self, William
Seal, Sudipta [1 ]
机构
[1] Univ Cent Florida, Nanosci Technol Ctr, Adv Mat Proc & Anal Ctr, Orlando, FL 32816 USA
[2] Univ Cent Florida, Dept Mech Mat & Aerosp Engn, Orlando, FL 32816 USA
[3] Univ Florida, Dept Chem Engn, Gainesville, FL 32611 USA
[4] Univ Cent Florida, Dept Mol Biol & Microbiol, Orlando, FL 32816 USA
关键词
cerium oxide nanoparticles; protein adsorption; cellular uptake; zeta potential; electrostatic interactions;
D O I
10.1016/j.biomaterials.2007.07.029
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The surface chemistry of biomaterials can have a significant impact on their performance in biological applications. Our recent work suggests that cerium oxide nanoparticles are potent antioxidants in cell culture models and we have evaluated several therapeutic applications of these nanoparticles in different biological systems. Knowledge of protein adsorption and cellular uptake will be very useful in improving the beneficial effects of cerium oxide nanoparticles in biology. In the present study, we determined the effect of zeta potential of cerium oxide nanoparticles on adsorption of bovine serum albumin (BSA) and cellular uptake in adenocarcinoma lung cells (A549). The zeta potential of the nanoparticles was varied by dispersing them in various acidic and basic pH solutions. UV-visible spectroscopy and inductively coupled plasma mass spectrometry (ICP-MS) were used for the protein adsorption and cellular uptake studies, respectively. Nanoceria samples having positive zeta potential were found to adsorb more BSA while the samples with negative zeta potential showed little or no protein adsorption. The cellular uptake studies showed preferential uptake for the negatively charged nanoparticles. These results demonstrate that electrostatic interactions can play an important factor in protein adsorption and cellular uptake of nanoparticles. Published by Elsevier Ltd.
引用
收藏
页码:4600 / 4607
页数:8
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