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

被引:0
|
作者
Yang, Jielai [1 ]
Zhan, Zihang [2 ]
Li, Xingchen [1 ]
Hu, Mu [1 ]
Zhu, Yuan [1 ]
Xiao, Yunchao [2 ]
Xu, Xiangyang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Ruijin Hosp, Shanghai Inst Traumatol & Orthopaed, Sch Med,Dept Orthopaed,Shanghai Key Lab Prevent &, Shanghai 200025, Peoples R China
[2] Jiaxing Univ, Coll Mat & Text Engn, Jiaxing 314001, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
3D-printing; Bredigite scaffold; Fullerol nanoparticle; Reactive oxygen species; Bone regeneration; OSTEOGENIC DIFFERENTIATION; CELL-INTERACTIONS; OSTEOCLASTOGENESIS; INHIBITION; MODULATION; IMPLANT; PROTEIN; REPAIR;
D O I
10.1016/j.mtbio.2024.101120
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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 via 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. In vitro, FPBS had good biocompatibility and excellent antioxidative capability. Furthermore, FPBS promoted the osteogenesis of stem cells with significant elevation of osteogenic markers. Finally, in vivo 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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页数:12
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