Enhanced bioactivity and osteoinductivity of carboxymethyl chitosan/nanohydroxyapatite/graphene oxide nanocomposites.
Enhanced bioactivity and osteoinductivity of carboxymethyl chitosan/nanohydroxyapatite/graphene oxide nanocomposites.
复制标题
羧甲基壳聚糖/纳米羟基磷灰石/氧化石墨烯纳米复合材料增强的生物活性和骨诱导性
DOI:
10.1039/c8ra00383a
复制
发表时间:
2018-05-14
期刊:
影响因子:
3.9
通讯作者:
Fan, Xianqun
中科院分区:
文献类型:
--
作者:
Yu, Zhang;Xiao, Caiwen;Huang, Yazhuo;Chen, Mingjiao;Wei, Wei;Yang, Xiaoxuan;Zhou, Huifang;Bi, Xiaoping;Lu, Linna;Ruan, Jing;Fan, Xianqun
Tissue engineering approaches combine a bioscaffold with stem cells to provide biological substitutes that can repair bone defects and eventually improve tissue functions. The prospective bioscaffold should have good osteoinductivity. Surface chemical and roughness modifications are regarded as valuable strategies for developing bioscaffolds because of their positive effects on enhancing osteogenic differentiation. However, the synergistic combination of the two strategies is currently poorly studied. In this work, a nanoengineered scaffold with surface chemistry (oxygen-containing groups) and roughness (Rq = 74.1 nm) modifications was fabricated by doping nanohydroxyapatite (nHA), chemically crosslinked graphene oxide (GO) and carboxymethyl chitosan (CMC). The biocompatibility and osteoinductivity of the nanoengineered CMC/nHA/GO scaffold was evaluated in vitro and in vivo, and the osteogenic differentiation mechanism of the nanoengineered scaffold was preliminarily investigated. Our data demonstrated that the enhanced osteoinductivity of CMC/nHA/GO may profit from the surface chemistry and roughness, which benefit the β1 integrin interactions with the extracellular matrix and activate the FAK–ERK signaling pathway to upregulate the expression of osteogenic special proteins. This study indicates that the nanocomposite scaffold with surface chemistry and roughness modifications could serve as a novel and promising bone substitute for tissue engineering.
登录
查看更多内容
影响因子:
12.7
作者:
Cai X;Xie J;Yao Y;Cun X;Lin S;Tian T;Zhu B;Lin Y
通讯作者:
Lin Y
影响因子:
14.8
作者:
通讯作者:
--
影响因子:
10
作者:
Genchi, Giada Graziana;Marino, Attilio;Ciofani, Gianni
通讯作者:
Ciofani, Gianni
影响因子:
2.4
作者:
Fujisaki, Kazuhiro;Tadano, Shigeru
通讯作者:
Tadano, Shigeru
影响因子:
12.7
作者:
Liao J;Tian T;Shi S;Xie X;Ma Q;Li G;Lin Y
通讯作者:
Lin Y