State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences , 1295 Dingxi Road, Shanghai 200050, China.
Xuhui District Central Hospital , 966 Middle Huaihai Road, Shanghai 200031, China.
ACS Appl Mater Interfaces. 2017 Feb 22;9(7):5757-5767. doi: 10.1021/acsami.6b14297. Epub 2017 Feb 8.
Silicate bioactive materials have been widely studied for bone regeneration because of their eminent physicochemical properties and outstanding osteogenic bioactivity, and different methods have been developed to prepare porous silicate bioactive ceramics scaffolds for bone-tissue engineering applications. Among all of these methods, the 3D-printing technique is obviously the most efficient way to control the porous structure. However, 3D-printed bioceramic porous scaffolds need high-temperature sintering, which will cause volume shrinkage and reduce the controllability of the pore structure accuracy. Unlike silicate bioceramic, bioactive silicate cements such as tricalcium silicate (CaSiO and CS) can be self-set in water to obtain high mechanical strength under mild conditions. Another advantage of using CS to prepare 3D scaffolds is the possibility of simultaneous drug loading. Herein, we, for the first time, demonstrated successful preparation of uniform 3D-printed CS bone cement scaffolds with controllable 3D structure at room temperature. The scaffolds were loaded with two model drugs and showed a loading location controllable drug-release profile. In addition, we developed a surface modification process to create controllable nanotopography on the surface of pore wall of the scaffolds, which showed activity to enhance rat bone-marrow stem cells (rBMSCs) attachment, spreading, and ALP activities. The in vivo experiments revealed that the 3D-printed CS bone cement scaffolds with nanoneedle-structured surfaces significantly improved bone regeneration, as compared to pure CS bone cement scaffolds, suggesting that 3D-printed CS bone cement scaffolds with controllable nanotopography surface are bioactive implantable biomaterials for bone repair.
硅酸盐水凝胶生物活性材料由于其优异的物理化学性能和出色的成骨生物活性而被广泛研究,为了满足骨组织工程应用的需要,已经开发出不同的方法来制备多孔硅酸盐水凝胶生物活性陶瓷支架。在所有这些方法中,3D 打印技术显然是控制多孔结构最有效的方法。然而,3D 打印的生物陶瓷多孔支架需要高温烧结,这会导致体积收缩,降低孔结构精度的可控性。与硅酸盐生物陶瓷不同,硅酸三钙(CaSiO 和 CS)等生物活性硅酸盐水泥可以在水中自凝固,在温和的条件下获得高机械强度。使用 CS 来制备 3D 支架的另一个优点是可以同时进行药物负载。在此,我们首次在室温下成功制备了均匀的 3D 打印 CS 骨水泥支架,其 3D 结构具有可控性。支架中负载了两种模型药物,并显示出具有负载位置可控释药特性的药物释放曲线。此外,我们开发了一种表面改性工艺,在支架的孔壁表面上创建了可控的纳米形貌,结果显示其对大鼠骨髓基质细胞(rBMSCs)黏附、铺展和碱性磷酸酶(ALP)活性有促进作用。体内实验表明,与纯 CS 骨水泥支架相比,具有纳米针状结构表面的 3D 打印 CS 骨水泥支架显著改善了骨再生,表明具有可控纳米形貌表面的 3D 打印 CS 骨水泥支架是一种用于骨修复的生物活性可植入生物材料。