A Psychrophilic GelMA: Breaking Technical and Immunological Barriers for Multimaterial High-Resolution 3D Bioprinting

Zaupa, Alessandro; Terraza, Claudia; Abarzua-Illanes, Phammela N.; Byres, Nicholas; Zavala, Gabriela; Cuenca, Jimena; Hidalgo, Carmen; Viafara-Garcia, Sergio M.; Wolf, Bettina; Pino-Lagos, Karina; Blaker, Jonny J.; Rumbak, Mayan; Khoury, Maroun; Enrione, Javier; Pablo Acevedo, Juan

Abstract

The increasing demand for tissue replacement has encouraged scientists worldwide to focus on developing new biofabrication technologies. Multimaterials/cells printed with stringent resolutions are necessary to address the high complexity of tissues. Advanced inkjet 3D printing can use multimaterials and attain high resolution and complexity of printed structures. However, a decisive yet limiting aspect of translational 3D bioprinting is selecting the befitting material to be used as bioink; there is a complete lack of cytoactive bioi n k s with adequate rheological, mechanical, and reactive properties. This work strives to achieve the right balance between resolution and cell support through methacrylamide functionalization of a psychrophilic gelatin and new fluorosurfactants used to engineer a photo-cross-linkable and immunoevasive bioink . The syntonized parameters following optimal formulation conditions allow proficient printability in a PolyJet 3D printer comparable in resolution to a commercial synthetic ink (similar to 150 mu m). The bioink formulation achieved the desired viabi l i t y (similar to 80%) and proliferation of co-printed cells w h i l e demonstrating in vivo immune tolerance of printed structures. The practical usage of existing high-resolution 3D printing systems using a novel bioink is shown here, allowing 3D bioprinted structures with potentially unprecedented complexity.

Más información

Título según WOS: ID WOS:000904597200001 Not found in local WOS DB
Título de la Revista: BIOMACROMOLECULES
Volumen: 24
Número: 1
Editorial: AMER CHEMICAL SOC
Fecha de publicación: 2023
Página de inicio: 150
Página final: 165
DOI:

10.1021/acs.biomac.2c01019

Notas: ISI