Thermodynamic 2D Silicene for Sequential and Multistage Bone Regeneration

被引:18
|
作者
Ni, Ni [1 ,2 ]
Ge, Min [3 ,4 ]
Huang, Rui [1 ,2 ]
Zhang, Dandan [1 ,2 ]
Lin, Han [3 ]
Ju, Yahan [1 ,2 ]
Tang, Zhimin [1 ,2 ]
Gao, Huiqin [1 ,2 ]
Zhou, Huifang [1 ,2 ]
Chen, Yu [5 ]
Gu, Ping [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Dept Ophthalmol, Sch Med, Shanghai 200011, Peoples R China
[2] Shanghai Key Lab Orbital Dis & Ocular Oncol, Shanghai 200011, Peoples R China
[3] Chinese Acad Sci, State Key Lab High Performance Ceram & Superfine M, Shanghai Inst Ceram, Shanghai 200050, Peoples R China
[4] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[5] Shanghai Univ, Sch Life Sci, Materdicine Lab, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
angiogenesis; proliferation; sequential bone repair; silicene; thermodynamics; CELL-PROLIFERATION; DIFFERENTIATION; NANOSHEETS; DELIVERY; REPAIR; LIGHT;
D O I
10.1002/adhm.202203107
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Bone healing is a multistage process involving the recruitment of cells, revascularization, and osteogenic differentiation, all of which are modulated in the temporal sequence to maximize cascade bone regeneration. However, insufficient osteoblast cells, poor blood supply, and limited bone induction at the site of critical-sized bone defect broadly impede bone repair. 2D SiO2-silicene@2,2 '-,azobis(2-[2-imidazolin-2-yl] propane) (SNSs@AIPH) with inherent thermodynamic property and osteoinductive activity is therefore designed and engineered for sequentially efficient bone repair. By means of controllable NIR-II irradiation, the integrated SNSs@AIPH stimulates the generation of appropriate intracellular reactive oxygen species, which accelerates early bone marrow mesenchymal stem cells (BMSCs) proliferation and angiogenesis remarkably. Importantly, as silicon-based 2D nanoparticles, the engineered SNSs@AIPH with high biocompatibility features distinct bioactivity to significantly promote BMSCs osteogenesis differentiation by activating TGF beta and BMP pathways. In a rat cranial defect model, SNSs@AIPH-NIR-II leads to a comparable increase of BMSCs proliferation and local vascularization at an early stage, followed by significant osteogenic differentiation, synergically resulting in a highly effective bone repair. Collectively, the fascinating characteristics and exceptional bone repair efficiency of NIR-II-mediated SNSs@AIPH allow it to be a promising bionic-oriented strategy for bone regeneration, broadening a new perspective in the application of cell-instructive biomaterials in bone tissue engineering.
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页数:17
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