Nanoporous diopside modulates biocompatibility, degradability and osteogenesis of bioactive scaffolds of gliadin-based composites for new bone formation

被引:18
作者
Ba, Zhaoyu [1 ]
Chen, Zhaoxiong [1 ]
Huang, Yufeng [1 ]
Feng, Du [2 ]
Zhao, Qinghui [3 ]
Zhu, Jianguang [1 ]
Wu, Desheng [1 ]
机构
[1] Tongji Univ, Sch Med, Shanghai East Hosp, Dept Spinal Surg, 150th Jimo Rd, Shanghai 200120, Peoples R China
[2] Guangzhou Med Univ, Inst Guangzhou Med Univ, Affiliated Canc Hosp, Sch Basic Med Sci,Key Lab Prot Modificat & Degrad, Guangzhou, Guangdong, Peoples R China
[3] Tongji Univ, Shanghai East Hosp, Biobank, Sch Med, Shanghai, Peoples R China
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2018年 / 13卷
基金
中国国家自然科学基金;
关键词
nanoporous diopside bioglass; gliadin; macro-nanoporous; MC3T3-E1; osteogenesis; DRUG-DELIVERY; STEM-CELLS; IN-VITRO; REPAIR; NANOCOMPOSITE; DIFFERENTIATION; PROPERTY; GRAPHENE; ZEIN;
D O I
10.2147/IJN.S162262
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Introduction: It is predicted that with increased life expectancy in the whole world, there will be a greater demand for synthetic biomedical materials to repair or regenerate lost, injured or diseased tissues. Natural polymers, as biomedical materials, have been widely applied in the field of regenerative medicine. Materials and methods: By incorporation of nanoporous diopside bioglass (nDPB) into gliadin (GL) matrix, macro-nanoporous scaffolds of nDPB/GL composites (DGC) were fabricated by method of solution compressing and particles leaching. Results: The results revealed that the DGC scaffolds possessed well-interconnected macropores of 200-500 mu m and nanopores of 4 nm, and the porosity and degradability of DGC scaffolds remarkably increased with the increase in nDPB content. In addition, in vitro cell experiments revealed that the adhesion and growth of MC3T3-E1 cells on DGC scaffolds were significantly promoted, which depended on nDPB content. Moreover, the results of histological evaluations confirmed that the osteogenic properties and degradability of DGC scaffolds in vivo significantly improved, which were nDPB content dependent. Furthermore, the results of immunohistochemical analysis demonstrated that, with the increase in nDPB content, the type I collagen expression in DGC scaffolds in vivo obviously enhanced, indicating excellent osteogenesis. Discussion and conclusion: The results demonstrated that the DGC scaffolds containing 30 wt% nDPB (30nDGC) exhibited good biocompatibility and new bone formation ability, which might have a great potential for applications in bone regeneration.
引用
收藏
页码:3883 / 3896
页数:14
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