Savoji Houman, Davenport Huyer Locke, Mohammadi Mohammad Hossein, Lun Lai Benjamin Fook, Rafatian Naimeh, Bannerman Dawn, Shoaib Mohammad, Bobicki Erin R, Ramachandran Arun, Radisic Milica
Institute of Biomaterials and Biomedical Engineering, University of Toronto, 170 College Street, Toronto, Ontario M5S 3G9, Canada.
Toronto General Research Institute, University Health Network, University of Toronto, 200 Elizabeth Street, Toronto, Ontario M5G 2C4, Canada.
ACS Biomater Sci Eng. 2020 Mar 9;6(3):1333-1343. doi: 10.1021/acsbiomaterials.9b00676. Epub 2020 Feb 11.
Bioelastomers have been extensively used in tissue engineering applications because of favorable mechanical stability, tunable properties, and chemical versatility. As these materials generally possess low elastic modulus and relatively long gelation time, it is challenging to 3D print them using traditional techniques. Instead, the field of 3D printing has focused preferentially on hydrogels and rigid polyester materials. To develop a versatile approach for 3D printing of elastomers, we used freeform reversible embedding of suspended prepolymers. A family of novel fast photocrosslinakble bioelastomer prepolymers were synthesized from dimethyl itaconate, 1,8-octanediol, and triethyl citrate. Tensile testing confirmed their elastic properties with Young's moduli in the range of 11-53 kPa. These materials supported cultivation of viable cells and enabled adhesion and proliferation of human umbilical vein endothelial cells. Tubular structures were created by embedding the 3D printed microtubes within a secondary hydrogel that served as a temporary support. Upon photocrosslinking and porogen leaching, the polymers were permeable to small molecules (TRITC-dextran). The polymer microtubes were assembled on the 96-well plates custom made by hot-embossing, as a tool to connect multiple organs-on-a-chip. The endothelialization of the tubes was performed to confirm that these microtubes can be utilized as vascular tubes to support parenchymal tissues seeded on them.
生物弹性体因其良好的机械稳定性、可调性能和化学多功能性,已在组织工程应用中得到广泛使用。由于这些材料通常具有低弹性模量和相对较长的凝胶化时间,使用传统技术对其进行3D打印具有挑战性。相反,3D打印领域优先关注水凝胶和刚性聚酯材料。为了开发一种用于弹性体3D打印的通用方法,我们使用了悬浮预聚物的自由形式可逆嵌入。由衣康酸二甲酯、1,8 - 辛二醇和柠檬酸三乙酯合成了一系列新型的快速光交联生物弹性体预聚物。拉伸测试证实了它们的弹性性能,杨氏模量在11 - 53 kPa范围内。这些材料支持活细胞的培养,并能使人脐静脉内皮细胞粘附和增殖。通过将3D打印的微管嵌入用作临时支撑的二次水凝胶中来创建管状结构。经过光交联和致孔剂浸出后,聚合物对小分子(TRITC - 葡聚糖)具有渗透性。聚合物微管被组装在通过热压印定制的96孔板上,作为连接多个芯片上器官的工具。对微管进行内皮化处理,以确认这些微管可作为血管微管来支持接种在其上的实质组织。