Enhanced physiochemical and mechanical performance of chitosan‐grafted graphene oxide for superior Osteoinductivity

J Ruan, X Wang, Z Yu, Z Wang, Q Xie… - Advanced Functional …, 2016 - Wiley Online Library
J Ruan, X Wang, Z Yu, Z Wang, Q Xie, D Zhang, Y Huang, H Zhou, X Bi, C Xiao, P Gu, X Fan
Advanced Functional Materials, 2016Wiley Online Library
The regeneration of artificial bone substitutes is a potential strategy for repairing bone
defects. However, the development of substitutes with appropriate osteoinductivity and
physiochemical properties, such as water uptake and retention, mechanical properties, and
biodegradation, remains challenging. Therefore, there is a motivation to develop new
synthetic grafts that possess good biocompatibility, physiochemical properties, and
osteoinductivity. Here, we fabricate a biocompatible scaffold through the covalent …
The regeneration of artificial bone substitutes is a potential strategy for repairing bone defects. However, the development of substitutes with appropriate osteoinductivity and physiochemical properties, such as water uptake and retention, mechanical properties, and biodegradation, remains challenging. Therefore, there is a motivation to develop new synthetic grafts that possess good biocompatibility, physiochemical properties, and osteoinductivity. Here, we fabricate a biocompatible scaffold through the covalent crosslinking of graphene oxide (GO) and carboxymethyl chitosan (CMC). The resulting GO‐CMC scaffold shows significant high water retention (44% water loss) compared with unmodified CMC scaffolds (120% water loss) due to a steric hindrance effect. The modulus and hardness of the GO‐CMC scaffold are 2.75‐ and 3.51‐fold higher, respectively, than those of the CMC scaffold. Furthermore, the osteoinductivity of the GO‐CMC scaffold is enhanced due to the π–π stacking interactions of the GO sheets, which result in striking upregulation of osteogenesis‐related genes, including osteopontin, bone sialoprotein, osterix, osteocalcin, and alkaline phosphatase. Finally, the GO‐CMC scaffold exhibits excellent reparative effects in repairing rat calvarial defects via the synergistic effects of GO and bone morphogenetic protein‐2. This study provides new insights for developing bone substitutes for tissue engineering and regenerative medicine.
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