4.4 Article

A novel natural-derived tilapia skin collagen mineralized with hydroxyapatite as a potential bone-grafting scaffold

期刊

JOURNAL OF BIOMATERIALS APPLICATIONS
卷 37, 期 2, 页码 219-237

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/08853282221086246

关键词

Natural-derived; tilapia skin collagen; hydroxyapatite; scaffold; osteogenesis

资金

  1. National Key R&D Program of China [2018YFC1106100, 2018YFC1106104]
  2. Youth Project of Shaanxi Natural Science Foundation [2020JQ-963]
  3. Basic Scientific Research project of Xi'an Jiaotong University [XZY012020055]
  4. National Natural Science Foundation of China [31870947]

向作者/读者索取更多资源

This study evaluated the potential use of collagen-based biomaterials from non-mammalian donors in bone repair. Tilapia skin collagen-hydroxyapatite scaffolds were successfully fabricated and showed promising microstructure, chemical, physical, and mechanical properties. In vitro studies demonstrated that the collagen/hydroxyapatite ratio of 1:4 had the most significant effect on the proliferation, differentiation, and mineralization of bone mesenchymal stem cells. In vivo experiments showed that the same ratio of scaffolds had excellent osteogenic activities in rat skull critical defections.
Collagen is widely used in medical field because of its excellent biocompatibility and bioactivity. To date, collagen for biomedical use is always derived from bovine or swine. The purpose of this study was to evaluate collagen-based biomaterials from non-mammalian donors for bone repair. Thus, tilapia skin collagen-hydroxyapatite (T-col/HAp) scaffolds were fabricated in three different proportions and then cross-linked with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide-N-hydroxysuccinimide (EDC-NHS). The scaffolds were evaluated for their microstructure, chemical and physical properties, mechanical strength and degradability. Then the in vitro responses of bone mesenchymal stem cells (BMSCs) to the scaffolds were investigated in terms of cellular proliferation, differentiation, and mineralization. At last, the scaffolds were implanted into rat skull critical defections to investigate the potential of osteogenic activities. As a result, the pore sizes and the porosities of the scaffolds were approximately 106.67-196.67 mu m and 81.5%-66.7%. Pure collagen group showed a mechanical strength of 0.065 MPa, and the mechanical strength was significantly enhanced almost 17 times and 32 times in collagen/HAp ratio 1:4 and 1:9 groups. In vitro studies revealed the most prominent and healthy growth of BMSCs in collagen/HAp ratio 1:4 group. All the scaffolds showed certain osteogenic activities and those loaded with small amount of hydroxyapatite showed the strongest bioactivities. The micro-CT showed that the critical bone defect was almost filled with generated bone 6 months after implantation in collagen/HAp ratio 1:4 group. The biomechanics tests further confirmed the highest generated bone strength was in the collagen/HAp ratio 1:4 group. This study indicated aquatic collagen might be a potential alternative for type I collagen from mammals in bone tissue engineering. The combination of collagen and inorganic materials was also important and appropriate inorganic component loading can achieve both osteogenic quality and osteogenic efficiency to a certain extent.

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