Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2008 Oct;3(5):637-45.
doi: 10.2217/17435889.3.5.637.

Reactive oxygen species scavenging properties of ZrO2-CeO2 solid solution nanoparticles

Affiliations

Reactive oxygen species scavenging properties of ZrO2-CeO2 solid solution nanoparticles

Yi-Yang Tsai et al. Nanomedicine (Lond). 2008 Oct.

Abstract

Aims: The hypothesis that an increase in defects in cerium oxide (CeO(2)) nanoparticles induced by solid solutions with differences in valency and ionic radius of the solute will yield superior reactive oxygen species (ROS) scavengers at room temperature will be tested.

Methods: Solid solutions of zirconium in CeO(2), that is, Ce(x)Zr(1-x)O(2) nanoparticles, were synthesized by a reverse micelle method. Their crystal structures, particle sizes and level of agglomeration were characterized. The nanoparticles' activities to scavenge ROS were tested in response to hydrogen peroxide at physiological levels and room temperature using an enzyme peroxidase-based assay.

Results: Solid solutions of Zr in CeO(2) nanoparticles enhanced ROS scavenging fourfold. The hypothesis is confirmed that more defects are formed and that the scavenging activities of Ce(x)Zr(1-x)O(2) correlate to the nanoparticles' oxygen-storage capacity.

Conclusions: The antioxidant efficacy of CeO(2) nanoparticles can be enhanced by dissolving zirconium in the CeO(2) lattice. The Ce(x)Zr(1-x)O(2) nanoparticles act as an enhanced catalyst at room temperature that scavenges ROS. Increased efficacy will enable lower nanoparticle dosages to protect cells from ROS, thus increasing the therapeutic width of these compounds.

PubMed Disclaimer

Publication types

LinkOut - more resources