3D gel printing of magnetic hydrogel scaffolds assisted by in-situ gelation in a water level-controlled crosslinker bath

被引:4
作者
Duan, Jing [1 ]
Lin, Tao [1 ]
Liu, Hongyuan [1 ]
Xu, Jing [1 ]
Shao, Huiping [1 ]
机构
[1] Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Beijing 100083, Peoples R China
关键词
3D printing; Magnetic hydrogels; Bone tissue; Scaffolds; CHITOSAN; NANOPARTICLES;
D O I
10.1016/j.ceramint.2023.01.160
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Polyvinylalcohol/chitosan (PVA/CS) is an excellent dual-network hydrogel material, but some significant challenges remain in fabricating composites with specific structures. In this study, 3D gel printing (3DGP) combined with a water-level controlled crosslinker bath was proposed for the rapid in-situ prototyping of PVA/ CS/Fe3O4 magnetic hydrogel scaffolds. Specifically, the PVA/CS/Fe3O4 hydrogels were extruded into the crosslinker water to achieve rapid in-situ gelation, improving the printability of hydrogel scaffolds. The effect of the PVA/CS ratio on the rheological and mechanical properties of dual-network magnetic hydrogels was eval-uated. The printing parameters were systematically optimized to facilitate the coordination between the cross -linking water bath and printer. The different crosslinking water baths were investigated to improve the printability of PVA/CS/Fe3O4 hydrogels. The results showed that the printability of the sodium hydroxide (NaOH) crosslinker was significantly better than that of sodium tripolyphosphate (TPP). The magnetic hydrogels (PVA: CS= 1: 1) crosslinked by NaOH had better compressive strength, swelling rate, and saturation magneti-zation of 1.17 MPa, 92.43%, and 22.19 emu/g, respectively. The MC3T3-E1 cell culture results showed that the PVA/CS/Fe3O4 scaffolds promoted cell adhesion and proliferation, and the scaffolds crosslinked by NaOH had superior cytocompatibility. 3DGP combined with a water-level controlled crosslinker bath offers a promising approach to preparing magnetic hydrogel materials.
引用
收藏
页码:15680 / 15688
页数:9
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