Keywords

Nanotechnology; Regenerative Medicine; Tissue Engineering; Biomedical Therapeutics; Biomaterials; Bone Tissue Regeneration

Abstract

Improper healing of bone fractures and limited regeneration of bone following bone tumor resection remain a prevalent complication worldwide. Long-term effects of this include joint instability, limited movement, and arthritis. Bone infections (osteomyelitis), reactive oxygen species (ROS) generation via excessive inflammation, and underlying conditions such as osteoporosis can contribute to suboptimal bone tissue regeneration. ROS accumulation stimulates osteoblast apoptosis, while promoting osteoclast differentiation. These processes inhibit mineralization and osteogenesis. Conventional therapeutics involve the utilization of drugs and bone grafts. However, these approaches pose limitations and can result in subsequent complications. Microbial infections, ROS accumulation, and excessive inflammations are factors that hinder endogenous bone tissue regeneration mechanisms. Thus, research has been focused on investigating interventional systems that promote osteoblast activity, combat microbial infections, stimulate free radical scavenging, and modulate inflammation. Recent studies with polycaprolactone revealed its potential to serve as an osteoinductive material due to its ability to support cell adhesion, migration, differentiation, and proliferation. Furthermore, silver exhibits antimicrobial activity, directs collagen and fibroblast formation, and enhances bone healing. Cerium oxide nanoparticles (CNPs) facilitate bone tissue regeneration by scavenging free radicals, mitigating inflammation, and preventing oxidative stress, thereby inhibiting apoptosis. Noting these properties, we integrated silver-doped CNPs within the polycaprolactone matrix to fabricate nanocomposite scaffolds. Comprehensive studies confirmed successful fabrication of nanocomposite scaffolds. In vitro cell viability assays revealed the nanocomposite scaffolds exhibited negligible cytotoxicity to human macrophages. Degradation assays showed favorable degradation of scaffolds under conditions mimicking the physiological environment. Superoxide dismutase assays confirmed the scaffolds’ free radical scavenging abilities. Bacterial inhibition assays showed the scaffolds posed bactericidal activity against Pseudomonas aeruginosa. Alkaline phosphatase assays, alizarin red stain, and qPCR will be utilized to assess the potential for the scaffolds to induce human mesenchymal stem cell differentiation into functional osteoblasts.

Thesis Completion Year

2025

Thesis Completion Semester

Spring

Thesis Chair

Seal, Sudipta

College

College of Engineering and Computer Science

Department

Materials Science and Engineering; Burnett School of Biomedical Sciences

Thesis Discipline

Biomaterials; Tissue Engineering

Language

English

Access Status

Open Access

Length of Campus Access

1 year

Campus Location

Orlando (Main) Campus

Available for download on Saturday, April 25, 2026

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Rights Statement

In Copyright