School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, China; National Engineering Research Centre for Tissue Restoration and Reconstruction, Guangzhou 510006, China.
School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, China; Guangdong Province Key Laboratory of Biomedical Engineering, South China University of Technology, Guangzhou 510006, China.
Carbohydr Polym. 2018 Oct 1;197:183-193. doi: 10.1016/j.carbpol.2018.05.086. Epub 2018 May 30.
Sol-gel derived organic/inorganic hybrids, in which organic and inorganic components form co-networks at the molecular level, have demonstrated great potential for providing improved mechanical properties and biological functions in tissue engineering applications. Here, a novel bioactive hydroxyapatite-chitosan-silica hybrid (HA-CSH) scaffold was successfully fabricated by combining the sol-gel method and 3D plotting technique. Physiochemical characterization confirmed that chitosan was hybridized homogeneously with the inorganic phase on nanoscale. The obtained scaffolds possessed precisely controllable and interconnected porous structures. The nano-sized HA formed in situ and dispersed uniformly in the hybrid network, which reduced the water absorption and increased the mechanical strength of the hybrid scaffold under humidity condition as compared to chitosan-silica hybrid (CSH) scaffold. Compression tests showed that the 3D plotted hybrid scaffolds under wet conditions had compressive strengths of 10-13 MPa and elastic moduli of 21-27 MPa and thus met the mechanical requirements of human trabecular bone. Studies on the mineralization process under simulated body fluid (SBF) conditions confirmed that the introduction of HA obviously increased the biological activity of hybrid scaffolds. In vitro cell results indicated that the HA-CSH scaffold not only supported adhesion and proliferation of mouse bone mesenchymal stem cells (mBMSCs), but also improved the osteoinductivity. The alkaline phosphatase activity and mineral deposition on the HA-CSH scaffold were higher than those on the CSH scaffold. These results suggested that the 3D plotted HA-CSH scaffold may be a promising bioactive material for bone tissues regeneration.
溶胶-凝胶衍生的有机/无机杂化材料,其中有机和无机成分在分子水平上形成共网络,在组织工程应用中显示出提供改善的机械性能和生物功能的巨大潜力。在这里,通过结合溶胶-凝胶法和 3D 绘图技术,成功制备了一种新型的生物活性羟基磷灰石-壳聚糖-硅杂化(HA-CSH)支架。物理化学特性证实壳聚糖在纳米尺度上与无机相均匀地杂化。所获得的支架具有精确可控和相互连通的多孔结构。原位形成的纳米级 HA 均匀分散在杂化网络中,与壳聚糖-硅杂化(CSH)支架相比,在湿度条件下降低了水吸收并提高了杂化支架的机械强度。压缩测试表明,在湿条件下 3D 绘制的杂化支架具有 10-13 MPa 的压缩强度和 21-27 MPa 的弹性模量,因此满足了人小梁骨的机械要求。在模拟体液(SBF)条件下的矿化过程研究证实,HA 的引入明显提高了杂化支架的生物活性。体外细胞结果表明,HA-CSH 支架不仅支持小鼠骨髓间充质干细胞(mBMSCs)的黏附和增殖,而且还提高了成骨诱导性。HA-CSH 支架上的碱性磷酸酶活性和矿化沉积高于 CSH 支架上的。这些结果表明,3D 绘制的 HA-CSH 支架可能是一种有前途的用于骨组织再生的生物活性材料。