Fullerol-reinforced antioxidantive 3D-printed bredigite scaffold for accelerating bone healing.

Mater Today Bio

Department of Orthopedics, Shanghai Institute of Traumatology and Orthopaedics, Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases, Ruijin Hospital, Shanghai Jiao Tong University, Shanghai, 200025, PR China.

Published: August 2024

AI Article Synopsis

  • Reactive oxygen species (ROS) are crucial for tissue repair, but an imbalance in redox homeostasis can hinder bone healing, necessitating better bone scaffold materials.
  • The study developed a 3D-printed biodegradable bio-scaffold (FPBS) using mussel-inspired polydopamine and nanoparticles that effectively scavenges ROS while promoting bone formation in a stressed environment.
  • FPBS demonstrated strong biocompatibility, enhanced stem cell osteogenesis, and significantly improved bone regeneration in a rat model, indicating its potential for effective bone defect repair.

Article Abstract

Reactive oxygen species play a vital role in tissue repair, and nonequilibrium of redox homeostasis around bone defect can compromise osteogenesis. However, insufficient antioxidant capacity and weak osteogenic performance remain major obstacles for bone scaffold materials. Herein, integrating the mussel-inspired polydopamine (PDA) coating and 3D printing technologies, we utilized the merits of both osteogenic bredigite and antioxidative fullerol to construct 3D-printed porous, biodegradable acid-buffering, reactive oxygen species (ROS) -scavenging and robust osteogenic bio-scaffold (denoted "FPBS") for in situ bone defect restoration under oxidative stress microenvironment. Initially, fullerol nanoparticles were attached to the surface of the bredigite scaffold covalently inter-crosslinking with PDA. Upon injury, extracellular ROS capturing triggered the oxidative degradation of PDA, releasing fullerol nanoparticles to enter into cells for further intracellular ROS scavenging. , FPBS had good biocompatibility and excellent antioxidative capability. Furthermore, FPBS promoted the osteogenesis of stem cells with significant elevation of osteogenic markers. Finally, implantation of FPBS remarkably enhanced new bone formation in a rat critical calvarial defect model. Overall, with amelioration of the ROS microenvironment of injured tissue and enhancement of osteogenic differentiation of stem cells simultaneously, FPBS may hold great potential towards bone defect repair.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11225861PMC
http://dx.doi.org/10.1016/j.mtbio.2024.101120DOI Listing

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