Wake Forest Institute for Regenerative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
School of Biomedical Engineering and Sciences, Wake Forest University-Virginia Tech, Winston-Salem, NC, United States of America.
Biofabrication. 2021 May 24;13(3). doi: 10.1088/1758-5090/abfd7a.
Digital light processing (DLP) bioprinting, which provides predominant speed, resolution, and adaptability for fabricating complex cell-laden three-dimensional (3D) structures, requires a combination of photoinitiator (PI) and UV absorber (UA) that plays critical roles during the photo-polymerization of bioinks. However, the PI and UA combination has not been highlighted for cell-based DLP bioprinting. In this study, the most used PIs and UAs in cell-based bioprinting were compared to optimize a combination that can ensure the maximum DLP printability, while maintaining the cellular activities during the process. The crosslinking time and printability of PIs were assessed, which are critical in minimizing the cell damage by the UV exposure during the fabrication process. On the other hand, the UAs were evaluated based on their ability to prevent the over-curing of layers beyond the focal layer and the scattering of light, which are required for the desirable crosslinking of a hydrogel and high resolution (25-50ms) to create a complex 3D cell-laden construct. Lastly, the cytotoxicity of PIs and UAs was assessed by measuring the cellular activity of 2D cultured and 3D bioprinted cells. The optimized PI and UA combination provided high initial cell viability (>90%) for up to 14 days in culture and could fabricate complex 3D structures like a perfusable heart-shaped construct with open vesicles and atriums. This combination can provide a potential starting condition when preparing the bioink for the cell-based DLP bioprinting in tissue engineering applications.
数字光处理(DLP)生物打印技术为制造复杂的细胞负载三维(3D)结构提供了卓越的速度、分辨率和适应性,需要光引发剂(PI)和紫外线吸收剂(UA)的组合,这在生物墨水的光聚合过程中起着关键作用。然而,基于细胞的 DLP 生物打印中尚未强调 PI 和 UA 的组合。在这项研究中,比较了用于基于细胞的生物打印的最常用的 PI 和 UA,以优化一种组合,该组合可以确保最大的 DLP 可打印性,同时在该过程中保持细胞活性。评估了 PI 的交联时间和可打印性,这对于最小化制造过程中 UV 暴露对细胞的损伤至关重要。另一方面,根据 UA 防止层间过度固化和光散射的能力进行了评估,这是水凝胶交联和高分辨率(25-50ms)所需的,以创建复杂的 3D 细胞负载结构。最后,通过测量 2D 培养细胞和 3D 生物打印细胞的细胞活性来评估 PI 和 UA 的细胞毒性。优化的 PI 和 UA 组合在培养中提供了高达 14 天的高初始细胞活力(>90%),并且可以制造复杂的 3D 结构,如具有开放小泡和心房的可灌注心形结构。当在组织工程应用中为基于细胞的 DLP 生物打印准备生物墨水时,该组合可以提供一个潜在的起始条件。