Nga Nguyen Kim, Thanh Tam Lai Thi, Ha Nguyen Thu, Hung Viet Pham, Huy Tran Quang
School of Chemical Engineering, Hanoi University of Science and Technology 1 Dai Co Viet Road Hanoi Vietnam
Research Center for Environmental Technology and Sustainable Development, Hanoi University of Science 334 Nguyen Trai Street Hanoi Vietnam.
RSC Adv. 2020 Nov 26;10(70):43045-43057. doi: 10.1039/d0ra09432c. eCollection 2020 Nov 23.
This work presents the enhanced biomineralization and protein adsorption capacity of 3D chitosan/hydroxyapatite (CS/HAp) biomimetic scaffolds synthesized from natural sources applied for bone-tissue engineering (BTE). The scaffolds were prepared by the freeze-drying method, then characterized by X-ray diffraction, scanning electron microscopy, liquid substitution, swelling behavior, and mechanical strength. Fourier transform infrared spectroscopy was also conducted to investigate the interaction between chitosan (CS) and hydroxyapatite (HAp). The biodegradation, biomineralization and protein adsorption capabilities of the scaffolds were evaluated through tests . Results showed that the 3D CS/HAp scaffolds exhibited highly porous structures with an average pore size of 265 μm, and mean porosity of 75.01%, respectively; the tensile strength of the scaffolds was 2.45 MPa, matching well with that of cancellous bone. The addition of HAp into the CS matrix efficiently decreased the swelling percentage of the CS/HAp scaffolds and retained the suitable degradation rate of the composite scaffolds; the degradation percentage of the CS/HAp scaffolds was 46.37% after 28 days immersed in a physiological solution. The CS/HAp scaffolds demonstrated a higher biomineralization capability than that of the CS scaffolds, releasing a bone-like apatite layer on their surface after 15 days of incubation in simulated body fluids. The presence of HAp mimicking biological apatite in the composite scaffolds facilitated a higher protein adsorption capability, compared to that of the CS scaffolds. The obtained results suggest that the CS/HAp scaffolds have great potential as biocompatible materials for BTE applications.
这项工作展示了由天然来源合成的用于骨组织工程(BTE)的三维壳聚糖/羟基磷灰石(CS/HAp)仿生支架增强的生物矿化和蛋白质吸附能力。通过冷冻干燥法制备支架,然后通过X射线衍射、扫描电子显微镜、液体置换、溶胀行为和机械强度对其进行表征。还进行了傅里叶变换红外光谱分析,以研究壳聚糖(CS)与羟基磷灰石(HAp)之间的相互作用。通过测试评估了支架的生物降解、生物矿化和蛋白质吸附能力。结果表明,三维CS/HAp支架呈现出高度多孔的结构,平均孔径分别为265μm,平均孔隙率为75.01%;支架的拉伸强度为2.45MPa,与松质骨的拉伸强度匹配良好。在CS基质中添加HAp有效地降低了CS/HAp支架的溶胀率,并保持了复合支架合适的降解速率;在生理溶液中浸泡28天后,CS/HAp支架的降解率为46.37%。CS/HAp支架表现出比CS支架更高的生物矿化能力,在模拟体液中孵育15天后,其表面释放出一层类骨磷灰石层。与CS支架相比,复合支架中模拟生物磷灰石的HAp的存在促进了更高的蛋白质吸附能力。所得结果表明,CS/HAp支架作为用于BTE应用的生物相容性材料具有巨大潜力。