High-resolution lithographic biofabrication of hydrogels with complex microchannels from low-temperature-soluble gelatin bioresins

• Published in: Materials today bio 2021-09, Vol.12, p.100162-100162, Article 100162
• Main Authors: Levato, Riccardo, Lim, Khoon S., Li, Wanlu, Asua, Ane Urigoitia, Peña, Laura Blanco, Wang, Mian, Falandt, Marc, Bernal, Paulina Nuñez, Gawlitta, Debby, Zhang, Yu Shrike, Woodfield, Tim B.F., Malda, Jos
• Format: Article
• Language: English
• Subjects: Biofabrication and bioprinting; Bioresin; Digital light processing; Full Length; Hydrogel; Lithography
• ISSN: 2590-0064; 2590-0064
• DOI: 10.1016/j.mtbio.2021.100162

Biofabrication via light-based 3D printing offers superior resolution and ability to generate free-form architectures, compared to conventional extrusion technologies. While extensive efforts in the design of new hydrogel bioinks lead to major advances in extrusion methods, the accessibility of lithographic bioprinting is still hampered by a limited choice of cell-friendly resins. Herein, we report the development of a novel set of photoresponsive bioresins derived from ichthyic-origin gelatin, designed to print high-resolution hydrogel constructs with embedded convoluted networks of vessel-mimetic channels. Unlike mammalian gelatins, these materials display thermal stability as pre-hydrogel solutions at room temperature, ideal for bioprinting on any easily-accessible lithographic printer. Norbornene- and methacryloyl-modification of the gelatin backbone, combined with a ruthenium-based visible light photoinitiator and new coccine as a cytocompatible photoabsorber, allowed to print structures resolving single-pixel features (∼50 ​μm) with high shape fidelity, even when using low stiffness gels, ideal for cell encapsulation (1–2 ​kPa). Moreover, aqueous two-phase emulsion bioresins allowed to modulate the permeability of the printed hydrogel bulk. Bioprinted mesenchymal stromal cells displayed high functionality over a month of culture, and underwent multi-lineage differentiation while colonizing the bioresin bulk with tissue-specific neo-deposited extracellular matrix. Importantly, printed hydrogels embedding complex channels with perfusable lumen (diameter