Disease Biophysics Group, Wyss Institute for Biologically Inspired Engineering, John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, United States of America.
Biofabrication. 2018 Jan 16;10(2):025004. doi: 10.1088/1758-5090/aa96de.
Organ-on-chip platforms aim to improve preclinical models for organ-level responses to novel drug compounds. Heart-on-a-chip assays in particular require tissue engineering techniques that rely on labor-intensive photolithographic fabrication or resolution-limited 3D printing of micropatterned substrates, which limits turnover and flexibility of prototyping. We present a rapid and automated method for large scale on-demand micropatterning of gelatin hydrogels for organ-on-chip applications using a novel biocompatible laser-etching approach. Fast and automated micropatterning is achieved via photosensitization of gelatin using riboflavin-5'phosphate followed by UV laser-mediated photoablation of the gel surface in user-defined patterns only limited by the resolution of the 15 μm wide laser focal point. Using this photopatterning approach, we generated microscale surface groove and pillar structures with feature dimensions on the order of 10-30 μm. The standard deviation of feature height was 0.3 μm, demonstrating robustness and reproducibility. Importantly, the UV-patterning process is non-destructive and does not alter gelatin micromechanical properties. Furthermore, as a quality control step, UV-patterned heart chip substrates were seeded with rat or human cardiac myocytes, and we verified that the resulting cardiac tissues achieved structural organization, contractile function, and long-term viability comparable to manually patterned gelatin substrates. Start-to-finish, UV-patterning shortened the time required to design and manufacture micropatterned gelatin substrates for heart-on-chip applications by up to 60% compared to traditional lithography-based approaches, providing an important technological advance enroute to automated and continuous manufacturing of organ-on-chips.
器官芯片平台旨在改进用于新型药物化合物的器官水平反应的临床前模型。特别是心脏芯片分析需要组织工程技术,这些技术依赖于劳动密集型的光刻制造或分辨率有限的微图案化基底的 3D 打印,这限制了原型制作的周转率和灵活性。我们提出了一种使用新颖的生物相容性激光刻蚀方法对用于器官芯片应用的明胶水凝胶进行大规模按需微图案化的快速自动化方法。通过核黄素-5'磷酸酯对明胶进行光敏化,然后仅通过用户定义的图案的 15μm 宽激光焦点的分辨率限制,使用 UV 激光介导对凝胶表面进行光烧蚀,从而实现快速自动化微图案化。使用这种光图案化方法,我们生成了具有 10-30μm 量级特征尺寸的微尺度表面槽和柱结构。特征高度的标准偏差为 0.3μm,表现出稳健性和可重复性。重要的是,UV 图案化过程是非破坏性的,不会改变明胶的微机械性能。此外,作为质量控制步骤,将 UV 图案化的心脏芯片基底接种大鼠或人心肌细胞,我们验证了所得的心脏组织实现了结构组织、收缩功能和与手动图案化明胶基底相当的长期存活能力。从头到尾,与传统的基于光刻的方法相比,UV 图案化将用于心脏芯片应用的微图案化明胶基底的设计和制造所需的时间缩短了多达 60%,为器官芯片的自动化和连续制造提供了重要的技术进步。