TY - GEN
T1 - Fast stereolithographic printing of large-scale vascularized tissue
AU - Anandakrishnan, Nanditha
AU - Ye, Hang
AU - Zhou, Chi
AU - Zhao, Ruogang
N1 - Publisher Copyright:
© 2019 Omnipress - All rights reserved.
PY - 2019
Y1 - 2019
N2 - Statement of Purpose: Large size engineered soft tissues hold great promise for tissue repair and organ transplantation, but their fabrication is faced with challenges in vascularization and achieving clinically-relevant size and shape. 3D bioprinting is an emerging technology for tissue fabrication; however, its application in large tissue fabrication is limited due to the difficulty to fabricate at multiple length scales and the slow printing speed1. Recently, the development of stereolithography (SLA)-based continuous liquid interface production (CLIP) technology enabled rapid printing of centimeter-thick parts in UV-curable resin2. However, the high viscosity of the resin along with the large suction force at the printing interface limited the printing capacity of the CLIP to only thin-walled parts. The fabrication of large-sized solid tissue is currently not achievable using CLIP. In this work, we present a Fast hydrogeL prOjection stereolithogrAphy Technology (FLOAT) that allows high speed fabrication of human scale solid hydrogel tissues containing perfusable vascular networks through a single, rapid printing process. We demonstrate the compatibility of the process with multiple photocurable hydrogel materials and the approaches to optimize the printing material for improved tissue regeneration, such as the endothelialization of pre-fabricated vascular channels while maintaining high encapsulated cell viability.
AB - Statement of Purpose: Large size engineered soft tissues hold great promise for tissue repair and organ transplantation, but their fabrication is faced with challenges in vascularization and achieving clinically-relevant size and shape. 3D bioprinting is an emerging technology for tissue fabrication; however, its application in large tissue fabrication is limited due to the difficulty to fabricate at multiple length scales and the slow printing speed1. Recently, the development of stereolithography (SLA)-based continuous liquid interface production (CLIP) technology enabled rapid printing of centimeter-thick parts in UV-curable resin2. However, the high viscosity of the resin along with the large suction force at the printing interface limited the printing capacity of the CLIP to only thin-walled parts. The fabrication of large-sized solid tissue is currently not achievable using CLIP. In this work, we present a Fast hydrogeL prOjection stereolithogrAphy Technology (FLOAT) that allows high speed fabrication of human scale solid hydrogel tissues containing perfusable vascular networks through a single, rapid printing process. We demonstrate the compatibility of the process with multiple photocurable hydrogel materials and the approaches to optimize the printing material for improved tissue regeneration, such as the endothelialization of pre-fabricated vascular channels while maintaining high encapsulated cell viability.
UR - http://www.scopus.com/inward/record.url?scp=85065419189&partnerID=8YFLogxK
M3 - Conference contribution
AN - SCOPUS:85065419189
T3 - Transactions of the Annual Meeting of the Society for Biomaterials and the Annual International Biomaterials Symposium
SP - 424
BT - Society for Biomaterials Annual Meeting and Exposition 2019
PB - Society for Biomaterials
T2 - 42nd Society for Biomaterials Annual Meeting and Exposition 2019: The Pinnacle of Biomaterials Innovation and Excellence
Y2 - 3 April 2019 through 6 April 2019
ER -