期刊
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
卷 192, 期 -, 页码 407-416出版社
ELSEVIER
DOI: 10.1016/j.ijbiomac.2021.09.036
关键词
Bone defect; Hydrogel scaffold; Osteogenesis; Hydroxyapatite; Stem cells; Bone Morphogenic protein
This study developed a dopamine adhesive chemistry-based silk fibroin hydrogel with nano-hydroxyapatite-graphene oxide hybrid nanofillers and immobilized bone morphogenic protein-2, which effectively promoted in vitro compatibility with rabbit bone marrow derived mesenchymal stem cells and in vivo new bone regrowth. Bone-specific hydrogel scaffolds with upgraded structural features and mechanical properties were achieved, showing promising results for new generation bone regeneration therapies.
Bone defect repair and tissue engineering is specifically challenging process because of the distinctive morphological and structural behaviours of natural bone with complex healing and biochemical mechanisms. In the present investigation, we designed dopamine adhesive chemistry-based fabrication of silk fibroin hydrogel (SFD) with incorporation of nano-hydroxyapatite (nHA)-graphene oxide (GO) hybrid nanofillers with wellarranged porous morphology immobilized with bone morphogenic protein-2 (BMP-2) for the effective in vitro rabbit bone marrow derived mesenchymal stem cells loading compatibility and in vivo new bone regrowth and collagen deposition ability. We have achieved bone-specific hydrogel scaffolds with upgraded structural features, mechanical properties and particularly promoted in vitro osteogenic differentiation and compatibility of rabbit bone marrow mesenchymal stem cells (rBMSCs). Structural and microscopic analyses established greater distributions of components and well-ordered and aligned porous structure of the hydrogel network. In vivo result of new bone regrowth was promisingly higher in the Bm@nHG-SFD hydrogel (85%) group as compared to the other treatment groups of nHG-SFD (77%) and nH-SFD (64%) hydrogel. Overall, we summarized that morphologically improved hydrogel material with immobilization of BMP-2 could be have more attentions for new generation bone regeneration therapies.
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