Additive manufacturing of hydroxyapatite–chitosan–genipin composite scaffolds for bone tissue engineering applications

京尼平 生物相容性 材料科学 组织工程 明胶 生物医学工程 自愈水凝胶 多孔性 壳聚糖 脚手架 复合数 复合材料 纳米技术 化学工程 化学 高分子化学 冶金 工程类 医学 生物化学
作者
Konstantinos Zafeiris,D. Brasinika,Anna Karatza,Elias P. Koumoulos,Ioannis K. Karoussis,Kyriaki Kyriakidou,Costas A. Charitidis
出处
期刊:Materials Science and Engineering: C [Elsevier BV]
卷期号:119: 111639-111639 被引量:93
标识
DOI:10.1016/j.msec.2020.111639
摘要

Additive manufacturing holds promise for the fabrication of three-dimensional scaffolds with precise geometry, to serve as substrates for the guided regeneration of natural tissue. In this work, a bioinspired approach is adopted for the synthesis of hybrid hydroxyapatite hydrogels, which were subsequently printed to form 3D scaffolds for bone tissue engineering applications. These hydrogels consist of hydroxyapatite nanocrystals, biomimetically synthesized in the presence of both chitosan and l -arginine. To improve their mechanical properties, chemical crosslinking was performed using a natural crosslinking agent (genipin), and their rheology was modified by employing an acetic acid/gelatin solution. Regarding the 3D printing process, several parameters (flow, infill and perimeter speed) were studied in order to accurately produce scaffolds with predesigned geometry and micro-architecture, while also applying low printing temperature (15 °C). Following the printing procedure, the 3D scaffolds were freeze dried in order to remove the entrapped solvents and therefore, obtain a porous interconnected network. Evaluation of porosity was performed using micro-computed tomography and nanomechanical properties were assessed through nanoindentation. Results of both characterization techniques, showed that the scaffolds' porosity as well as their modulus values, fall within the corresponding range of the respective values of cancellous bone. The biocompatibility of the 3D printed scaffolds was assessed using MG63 human osteosarcoma cells for 7 days of culturing. Cell viability was evaluated by MTT assay as well as double staining and visualized under fluorescence microscopy, while cell morphology was analyzed through scanning electron microscopy. Biocompatibility tests, revealed that the scaffolds constitute a cell-friendly environment, allowed them to adhere on the scaffolds' surface, increase their population and maintain high levels of viability.
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