生物相容性
材料科学
碱性磷酸酶
纳米复合材料
运行x2
结晶度
复合数
明胶
壳聚糖
骨钙素
核化学
化学工程
纳米技术
复合材料
化学
生物化学
冶金
工程类
酶
作者
Shangsi Chen,Yufei Shi,Xin Zhang,Jun Ma
摘要
Abstract In this study, we have successfully fabricated magnesium (Mg) substituted hydroxyapatite nanocomposites (Mg‐HA) by utilizing type I collagen (COL I) and citric acid (CA) through a bitemplate‐induced biomimetic mineralization approach. The obtained composite nanoparticles were subsequently mixed with chitosan (CHI) and gelatin (Gel) to prepare porous scaffolds with interconnected structures by three‐dimensional (3D) printing technique. The Mg‐HA powders and composite scaffolds were characterized. The results showed that the substitution of Mg for Ca ions reduced the crystallinity of HA crystals, but did not significantly affect the size and structure of the nanocomposites. The morphology of Mg‐HA scaffolds turned smoother compared with the HA scaffolds with Mg substitution. Furthermore, the biocompatibility of Mg‐HA composite scaffolds was evaluated by metal ion release, cell attachment, proliferation, and differentiation of MC3T3‐E1 cells. According to the results, as the more Ca 2+ was substituted by Mg 2+ , the more Mg 2+ was released from the samples and the pH in cultured medium was more acidic. It was suggested that Mg‐HA scaffolds presented higher cell attachment, proliferation rate, increased expression of alkaline phosphatase (ALP) activity and osteogenic related gene, including osteocalcin (OCN), runt‐related transcription factor 2 (RUNX2), and COL I. Therefore, it was indicated that the 3D printed Mg‐HA composite scaffolds with excellent biocompatibility and bioactivity were a potential candidate in bone tissue engineering.
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