Institute for Medical Devices Control, National Institutes for Food and Drug Control, Beijing 102629, PR China; School of Materials Science and Engineering, Beihang University, Beijing 100191, PR China.
Department of Biomedical Engineering, School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, PR China; National Engineering Research Center for Tissue Restoration and Reconstruction, South China University of Technology, Guangzhou 510006, PR China.
Mater Sci Eng C Mater Biol Appl. 2020 Nov;116:111148. doi: 10.1016/j.msec.2020.111148. Epub 2020 Jun 2.
Three-dimensional (3D) printing technology has attracted considerable focus for preparing porous bone repair scaffolds to promote bone regeneration. Inspired by organic-inorganic components and the porous structure of natural bone, novel porous degradable scaffolds have been printed using hydroxyapatite (HA), carboxymethyl chitosan (CMCS), and polydopamine (PDA). The well-designed HA/CMCS/PDA scaffolds exhibited a porous structure with 60.5 ± 4.6% porosity and 415 ± 87 μm in mode pore diameter. The weight loss percentage (WL%) of the HA/CMCS/PDA scaffolds reached about 17% during a 10-week degradation in vitro. The degradation process between the CMCS and HA induced the release of calcium ions. Using commercial product as the contrast material, the osteogenic properties of the scaffolds were assessed in vivo. The implantation and degradation of HA/CMCS/PDA scaffolds had no adverse effects on the kidney and liver of rabbits with no inflammatory response in the implantation sites. The micro-CT and histology data suggested that the HA/CMCS/PDA scaffolds could effectively stimulate new bone formation within the femoral lacuna defect region of rabbits versus blank control at 12 weeks after implantation. Surface cortical bone was generated in the defect area in the HA/CMCS/PDA group; the defect in the blank group remained obvious. HA/CMCS/PDA scaffolds had excellent biodegradability matching the formation of new bone during implantation. In conclusion, 3D-printed HA/CMCS/PDA scaffolds have remarkable potential as a new material for repairing bone defects.
三维(3D)打印技术因其能够制备促进骨再生的多孔骨修复支架而受到广泛关注。受有机-无机成分和天然骨多孔结构的启发,使用羟基磷灰石(HA)、羧甲基壳聚糖(CMCS)和聚多巴胺(PDA)打印了新型多孔可降解支架。设计良好的 HA/CMCS/PDA 支架具有多孔结构,孔隙率为 60.5±4.6%,模式孔径为 415±87μm。在体外 10 周的降解过程中,HA/CMCS/PDA 支架的重量损失百分比(WL%)达到约 17%。CMCS 和 HA 之间的降解过程诱导钙离子释放。使用商业产品作为对照材料,评估了支架的体内成骨性能。HA/CMCS/PDA 支架的植入和降解对兔的肾脏和肝脏没有不良影响,植入部位也没有炎症反应。微 CT 和组织学数据表明,与空白对照组相比,植入后 12 周,HA/CMCS/PDA 支架可有效刺激兔股骨腔隙缺损区域的新骨形成。在 HA/CMCS/PDA 组的缺损区域生成了表面皮质骨,而空白组的缺损仍然很明显。HA/CMCS/PDA 支架具有优异的生物降解性,与植入过程中形成的新骨相匹配。总之,3D 打印的 HA/CMCS/PDA 支架作为修复骨缺损的新材料具有显著的潜力。