Biomimetic synthesis of Mg‐substituted hydroxyapatite nanocomposites and three‐dimensional printing of composite scaffolds for bone regeneration. Issue 11 (26th July 2019)

• Record Type: Journal Article
• Authors: Chen, Shangsi; Shi, Yufei; Zhang, Xin; Ma, Jun
• Is Part Of: Journal of biomedical materials research. Volume 107:Issue 11(2019)
• Page Start: 2512
• Page End: 2521
• Publication Date: 2019-07-26
• Subjects: 3D printing -- bone tissue engineering -- composite scaffolds -- hydroxyapatite -- magnesium; Biomedical materials -- Periodicals; 610.28
• DOI: 10.1002/jbm.a.36757
• Languages: English
• ISSNs: 1549-3296

Abstract

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.