细菌纤维素
生物活性玻璃
纳米复合材料
材料科学
脚手架
生物相容性
碱性磷酸酶
介孔材料
间质细胞
生物医学工程
化学
纤维素
纳米技术
复合材料
生物化学
医学
冶金
催化作用
酶
病理
作者
Jian Xiao,Qianghua Wei,Jinhong Xue,Zhicong Liu,Zhen Li,Zifa Zhou,Fu Chen,Fulai Zhao
标识
DOI:10.1016/j.colsurfa.2022.128693
摘要
In this study, a nanocomposite scaffold composed of mesoporous bioactive glass/bacterial cellulose (MBG/BC) has been synthesized using an in situ membrane-liquid interface culture. In the resulting MBG/BC nanocomposites, MBG is homogeneously distributed in the three-dimensional BC matrix. In vitro mineralization experiments revealed that incorporating MBG into BC scaffolds enhanced their bioactivity. Subsequently, human bone marrow stromal cells (hMBSCs) were seeded onto MBG/BC scaffolds, and the effect of MBG on biocompatibility and bone regeneration was evaluated by analyzing the cell morphology, measuring cell viability, alkaline phosphatase (ALP) activity, and osteogenic-related gene expression. The results showed that MBG/BC nanocomposite scaffolds exhibited an increase in hMBSC proliferation, ALP activity, and osteogenic-related gene expression compared to bare BC scaffolds. We believe that the scalable and simple green method can be used in fabricating other BC-based nanocomposite scaffolds, and that the MBG/BC scaffolds are considered a promising candidate for treatment of bone defects. In this study, a novel membrane-liquid interface culturing method for the preparation of 3D MBG/BC nanocomposite scaffolds has been proposed. Unlike conventional static culture method, this method can not only produce thick MBG/BC nanocomposites but also ensure the uniform distribution of MBG nanofibers throughout the samples at any arbitrary thickness. Furthermore, it is a scalable, versatile, and ecofriendly method. • A novel three-dimensional scaffold was prepared by the layer-by-layer (LBL) interface culture method. • This scaffold was composed of mesoporous bioactive glass and bacterial cellulose nanofibers. • The scaffold possessed excellent in vitro bioactivity. • The nanocomposite scaffold showed improved cell proliferation, ALP activity and osteogenic-related gene expression.
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