Keywords

Cerium; Wound Healing; Reactive Oxygen Species; Material doping

Abstract

Ceria nanoparticles' capabilities to defend cells against oxidative stress through superoxide dismutase activity are well-documented. Ceria nanoparticles demonstrate a ratio between 3+/4+ oxidative states on the surface of the particles to exhibit oxygen vacancies, a feature that allows these particles to scavenge Reactive Oxygen Species (ROS) in times of Oxidative Stress. Oxidative stress arises from many wounds in the body, such as wounds in the skin, and can have significant impacts on the health of an individual. Even when receiving treatment for the skin wound, ROS can circulate from around the wound, be generated from an imbalance in antioxidants, or enter from the environment. These ROS can further delay the healing of wounds or exacerbate issues, causing irreparable harm to cells and DNA around the wound site. Ceria nanoparticles have been utilized in the past to perform targeted drug delivery into the body and have been vastly investigated for their ability to scavenge ROS. To utilize both the drug-delivery and scavenging aspects of ceria nanoparticles, this paper will investigate the ability of metal-doped ceria nanoparticles to scavenge ROS during times of oxidative stress. The experimentation will involve Gold (Au), Zinc (Zn), Iron (Fe), Copper (Cu), and Strontium (Sr) utilized as the metals for doping the ceria nanoparticles. This topic poses a novel approach to wound healing, as utilizing a dual-use approach to CNP drug delivery can provide significant therapeutic advances.

Thesis Completion Year

2025

Thesis Completion Semester

Spring

Thesis Chair

Seal, Sudipta

College

College of Engineering and Computer Science

Department

Materials Science and Engineering

Thesis Discipline

Materials Science

Language

English

Access Status

Open Access

Length of Campus Access

None

Campus Location

Orlando (Main) Campus

Available for download on Saturday, April 25, 2026

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Rights Statement

In Copyright