The objective of this study was to develop a collagen/hydroxyapatite (HA) nanocomposite scaffold for bone tissue engineering applications. For this purpose, in situ mineralization of HA was accompanied with formation of collagen hydrogel at condition similar to the physiological condition, pH = 7.4, and 37 C. The physicochemical and biological properties of the in situ scaffold were compared with nanocomposite fabricated by mixing HA powder and collagen hydrogel (powder-mixed scaffold). The HA in this method was formed in the same condition as the in situ method. X-ray diffraction and FTIR analysis of in situ scaffold showed the formation of carbonated HA, similar to bone, while the HA powder in powder-mixed scaffold showed non-carbonated structure. Scanning electron microscopy revealed the formation of fibrillated collagen in both composites. HA was observed in both scaffolds, but with different morphology. The in situ formed HA had a plate-like morphology while the preformed HA showed spherical morphology in the powder-mixed scaffold. The invitro cytocompatibility and osteogenesis activity of scaffolds using osteoblast-like cells (MG-63) showed higher cytocompatibility and more osteogenesis capability of the in situ scaffold in comparison with the powder-mixed scaffold. The results suggest the in situ method as a proper approach for fabrication of HA/collagen scaffolds with similar properties like bone.
The aim of this study was to investigate the effect of developed collagen (Co) hydrogel (CH), powder-mixed hydroxyapatite/collagen (HA/Co) hydrogel and in situ synthesized HA/Co (In/HA/Co) hydrogel with or without mesenchymal stem cell (MSC) and platelet-rich plasma (PRP) on the regeneration of fullthickness critical size bone defect in the rabbit animal model. In the first step of this study, the scaffolds were synthesized and characterized using FTIR spectroscopy, X-ray diffraction, and scanning electron microcopy. In the second step or animal study, the radial bone defects were filled with the synthesized scaffolds with and without MSC and PRP. One hundred sixty one year-old New Zealand white male rabbits were randomly divided in 16 groups of 10 rabbits including control
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