Automated fabrication of photopatterned gelatin hydrogels for organ-on-chips applications

被引:46
作者
Nawroth, Janna C. [1 ,3 ]
Scudder, Lisa L. [1 ]
Halvorson, Ryan T. [1 ]
Tresback, Jason [2 ]
Ferrier, John P., Jr. [1 ]
Sheehy, Sean P. [1 ]
Cho, Alex [1 ]
Kannan, Suraj [1 ]
Sunyovszki, Ilona [1 ]
Goss, Josue A. [1 ]
Campbell, Patrick H. [1 ]
Parker, Kevin Kit [1 ]
机构
[1] Harvard Univ, John A Paulson Sch Engn & Appl Sci, Wyss Inst Biol Inspired Engn, Dis Biophys Grp, Cambridge, MA 02138 USA
[2] Harvard Univ, Ctr Nanoscale Syst, Cambridge, MA 02138 USA
[3] Emulate Inc, Boston, MA USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
tissue engineering; heart-on-a-chip; optical patterning; hydrogel fabrication; micropatterning; cell culture substrate; CELL-DERIVED CARDIOMYOCYTES; ENGINEERED CARDIAC TISSUES; CORNEAL CROSS-LINKING; IN-VITRO MODEL; STEM-CELL; DIMENSIONS; HEART; SURFACE; MYOCYTES; MUSCLE;
D O I
10.1088/1758-5090/aa96de
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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 mu m 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 mu m. The standard deviation of feature height was 0.3 mu m, 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.
引用
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页数:15
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