Department of Cardiothoracic Surgery and Stanford University, Stanford, California, USA.
Department of Bioengineering, Stanford University, Stanford, California, USA.
Tissue Eng Part C Methods. 2023 Mar;29(3):85-94. doi: 10.1089/ten.TEC.2022.0214. Epub 2023 Mar 2.
Three-dimensional (3D) bioprinting demonstrates technology that is capable of producing structures comparable to native tissues in the human body. The freeform reversible embedding of suspended hydrogels (FRESH) technique involves hydrogel-based bio-inks printed within a thermo-reversible support bath to provide mechanical strength to the printed construct. Smaller and more uniform microsphere sizes of FRESH were reported to aid in enhancing printing resolution and construct accuracy. Therefore, we sought to optimize the FRESH generation protocol, particularly by varying stir speed and stir duration, in hopes to further improve microsphere size and uniformity. We observed optimal conditions at a stir speed of 600 rpm and stir duration for 20 h that generated the smallest microspheres with the best uniformity. Comparison of using the optimized FRESH to the commercial FRESH LifeSupport to bioprint single filament and geometrical constructs revealed reduced single filament diameters and higher angular precision in the optimized FRESH bio-printed constructs compared with those printed in the commercial FRESH. Overall, our refinement of the FRESH manufacturing protocol represents an important step toward enhancing 3D bioprinting resolution and construct fidelity. Improving such technologies allows for the fabrication of highly accurate constructs with anatomical properties similar to native counterparts. Such work has significant implications in the field of tissue engineering for producing accurate human organ model systems. Impact statement Freeform reversible embedding of suspended hydrogels (FRESH) is a method of sacrificial three-dimensional (3D) bioprinting that offers support to reinforce bio-ink extrusion during printing. During FRESH generation, the stir speed and stir duration of the mixture can significantly impact FRESH microsphere characteristics. In this study, we optimized FRESH microspheres to significantly improve resolution and accuracy in bioprinting. This advancement in FRESH-based 3D bioprinting technologies allows for the fabrication of highly accurate constructs with anatomical properties similar to native counterparts and has significant implications in the field of tissue engineering and translational medicine.
三维(3D)生物打印技术能够制造出与人体组织相似的结构。自由可逆嵌入悬浮水凝胶(FRESH)技术涉及基于水凝胶的生物墨水打印在热可逆支撑浴中,为打印结构提供机械强度。据报道,更小且更均匀的 FRESH 微球尺寸有助于提高打印分辨率和构建精度。因此,我们试图优化 FRESH 生成方案,特别是通过改变搅拌速度和搅拌时间,希望进一步改善微球尺寸和均匀性。我们观察到在搅拌速度为 600 rpm 和搅拌时间为 20 h 的最佳条件下,生成的微球最小且均匀性最好。将优化后的 FRESH 与商用 FRESH LifeSupport 进行生物打印单丝和几何结构的比较表明,与商用 FRESH 打印的结构相比,优化后的 FRESH 生物打印的单丝直径更小,角精度更高。总体而言,我们对 FRESH 制造方案的改进是提高 3D 生物打印分辨率和构建保真度的重要步骤。此类技术的改进可以制造出具有与天然对应物相似解剖特性的高度精确的结构。这项工作在制造精确的人体器官模型系统方面对组织工程领域具有重要意义。