García-García Ane, Pérez-Álvarez Leyre, Ruiz-Rubio Leire, Larrea-Sebal Asier, Martin Cesar, Vilas-Vilela José Luis
Grupo de Química Macromolecular (LABQUIMAC), Departamento de Química Física, Facultad de Ciencia y Tecnología, Universidad del País Vasco (UPV/EHU), 48940 Leioa, Spain.
BCMaterials, Basque Center for Materials, Applications and Nanostructures, UPV/EHU Science Park, 48940 Leioa, Spain.
Gels. 2024 Feb 4;10(2):126. doi: 10.3390/gels10020126.
Photocuring of chitosan has shown great promise in the extrusion-based 3D printing of scaffolds for advanced biomedical and tissue engineering applications. However, the poor mechanical stability of methacrylated chitosan photocuring ink restricts its applicability. The inclusion of co-networks by means of simultaneous polycomplex formation is an effective method by which to solve this drawback, but the formed hydrogel inks are not printable. This work aims to develop new photocurable chitosan inks based on the simultaneous photocrosslinking of methacrylated chitosan (CHIMe) with N,N'-methylenebisacrylamide, polyethylene glycol diacrylate, and acrylic acid to be applied in extrusion 3D printing. Interestingly, the polycomplex co-network corresponding to the acrylic-acid-based ink could be successfully printed by the here-presented simultaneous photocuring strategy. Further, the conversion of photocrosslinking was studied via photo-DSC analyses that revealed a clear dependence on the chemical structure of the employed crosslinking agents (from 40 to ~100%). In addition, the mechanical and rheological properties of the photocured hydrogels were comparatively studied, as well as the printing quality of the extruded scaffolds. The newly developed chitosan photocurable inks demonstrated extrusion printability (squareness ~0.90; uniformity factor ~0.95) and tunable mechanical properties (Young modulus 14-1068 Pa) by means of different crosslinking approaches according to the chemical architecture of the reactive molecules employed. This work shows the great potential of photocrosslinkable chitosan inks.
壳聚糖的光固化在用于先进生物医学和组织工程应用的基于挤出的支架3D打印中显示出巨大的前景。然而,甲基丙烯酸化壳聚糖光固化油墨较差的机械稳定性限制了其适用性。通过同时形成聚络合物来引入共网络是解决这一缺点的有效方法,但形成的水凝胶油墨不可打印。这项工作旨在开发基于甲基丙烯酸化壳聚糖(CHIMe)与N,N'-亚甲基双丙烯酰胺、聚乙二醇二丙烯酸酯和丙烯酸同时光交联的新型光固化壳聚糖油墨,用于挤出3D打印。有趣的是,通过本文提出的同时光固化策略,可以成功打印出与丙烯酸基油墨对应的聚络合物共网络。此外,通过光DSC分析研究了光交联的转化率,结果表明其明显依赖于所用交联剂的化学结构(从40%到100%)。此外,还对光固化水凝胶的力学和流变性能以及挤出支架的打印质量进行了比较研究。新开发的壳聚糖光固化油墨通过根据所用反应分子的化学结构采用不同的交联方法,展示了挤出可打印性(方形度0.90;均匀性因子~0.95)和可调的力学性能(杨氏模量14-1068 Pa)。这项工作展示了光交联壳聚糖油墨的巨大潜力。