Novel synthesis of cerium oxide nanoparticles for free radical scavenging

被引:86
|
作者
Tsai, Yi-Yang
Oca-Cossio, Jose
Agering, Kristina
Simpson, Nicholas E.
Atkinson, Mark A.
Wasserfall, Clive H.
Constantinidis, Ioannis
Sigmund, Wolfgang [1 ]
机构
[1] Univ Florida, Dept Mat Sci & Engn, Gainesville, FL USA
[2] Univ Florida, Dept Med, Div Endocrinol, Gainesville, FL USA
[3] Univ Florida, Coll Med, Dept Pathol, Gainesville, FL USA
关键词
antioxidant; cerium oxide; free radical scavenging; nanoparticles; reverse micelle method;
D O I
10.2217/17435889.2.3.325
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: The aim of this article is to present a novel synthetic route to form CeO2 nanoparticles that protects against the detrimental influence of oxidative stress in mammalian cells. Methods: The noncytotoxic surfactant lecithin was used to synthesize CeO2 nanoparticles and the products were colloidally stabilized in a biocompatible tri-sodium citrate buffer. These nanoparticles were delivered into murine insulinoma beta TC-tet cells, and intracellular free radical concentrations responding to exposure to hydroquinone were measured in a variety of extracellular CeO2 concentrations. Results: Well-dispersed, highly crystallized CeO2 nanoparticles of 3.7 nm in size were achieved that are chemically and colloidally stable in Dulbecco's modified Eagle's medium for extended periods of time. Treating beta TC-tet cells with these nanoparticles alleviated detrimental intracellular free radical levels down to the primary level. Conclusion: CeO2 nanoparticles synthesized from this route are demonstrated to be effective free radical scavengers within beta TC-tet cells. Furthermore, it is shown that CeO2 nanoparticles provide an effective means to improve cellular survival in settings wherein cell loss due to oxidative stress limits native function.
引用
收藏
页码:325 / 332
页数:8
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