TY - JOUR
T1 - Tunable and Compartmentalized Multimaterial Bioprinting for Complex Living Tissue Constructs
AU - Hassan, Shabir
AU - Gomez-Reyes, Eduardo
AU - Enciso-Martinez, Eduardo
AU - Shi, Kun
AU - Campos, Jorge Gonzalez
AU - Soria, Oscar Yael Perez
AU - Luna-Cerón, Eder
AU - Lee, Myung Chul
AU - Garcia-Reyes, Isaac
AU - Steakelum, Joshua
AU - Jeelani, Haziq
AU - García-Rivera, Luis Enrique
AU - Cho, Minsung
AU - Cortes, Stephanie Sanchez
AU - Kamperman, Tom
AU - Wang, Haihang
AU - Leijten, Jeroen
AU - Fiondella, Lance
AU - Shin, Su Ryon
N1 - Funding Information:
This work was supported by the National Institutes of Health (R01AR074234, R21EB026824, R01AR073822, R01AR077132), AHA Innovative Project Award (19IPLOI34660079), the Gillian Reny Stepping Strong Center for Trauma Innovation, and the Brigham Research Institute Innovation Evergreen Fund (IEF) at Brigham and Women’s Hospital. M.C.L. was supported by Basic Science Research Program through the National Research Foundation of Korea(NRF) funded by the Ministry of Education(NRF-2021R1A6A3A14039720). T.K. acknowledges funding from a Rubicon award (019.183EN.017) by the Dutch Research Council (NWO).
Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022/11/8
Y1 - 2022/11/8
N2 - Recapitulating inherent heterogeneity and complex microarchitectures within confined print volumes for developing implantable constructs that could maintain their structure in vivo has remained challenging. Here, we present a combinational multimaterial and embedded bioprinting approach to fabricate complex tissue constructs that can be implanted postprinting and retain their three-dimensional (3D) shape in vivo. The microfluidics-based single nozzle printhead with computer-controlled pneumatic pressure valves enables laminar flow-based voxelation of up to seven individual bioinks with rapid switching between various bioinks that can solve alignment issues generated during switching multiple nozzles. To improve the spatial organization of various bioinks, printing fidelity with the z-direction, and printing speed, self-healing and biodegradable colloidal gels as support baths are introduced to build complex geometries. Furthermore, the colloidal gels provide suitable microenvironments like native extracellular matrices (ECMs) for achieving cell growths and fast host cell invasion via interconnected microporous networks in vitro and in vivo. Multicompartment microfibers (i.e., solid, core-shell, or donut shape), composed of two different bioink fractions with various lengths or their intravolume space filled by two, four, and six bioink fractions, are successfully printed in the ECM-like support bath. We also print various acellular complex geometries such as pyramids, spirals, and perfusable branched/linear vessels. Successful fabrication of vascularized liver and skeletal muscle tissue constructs show albumin secretion and bundled muscle mimic fibers, respectively. The interconnected microporous networks of colloidal gels result in maintaining printed complex geometries while enabling rapid cell infiltration, in vivo.
AB - Recapitulating inherent heterogeneity and complex microarchitectures within confined print volumes for developing implantable constructs that could maintain their structure in vivo has remained challenging. Here, we present a combinational multimaterial and embedded bioprinting approach to fabricate complex tissue constructs that can be implanted postprinting and retain their three-dimensional (3D) shape in vivo. The microfluidics-based single nozzle printhead with computer-controlled pneumatic pressure valves enables laminar flow-based voxelation of up to seven individual bioinks with rapid switching between various bioinks that can solve alignment issues generated during switching multiple nozzles. To improve the spatial organization of various bioinks, printing fidelity with the z-direction, and printing speed, self-healing and biodegradable colloidal gels as support baths are introduced to build complex geometries. Furthermore, the colloidal gels provide suitable microenvironments like native extracellular matrices (ECMs) for achieving cell growths and fast host cell invasion via interconnected microporous networks in vitro and in vivo. Multicompartment microfibers (i.e., solid, core-shell, or donut shape), composed of two different bioink fractions with various lengths or their intravolume space filled by two, four, and six bioink fractions, are successfully printed in the ECM-like support bath. We also print various acellular complex geometries such as pyramids, spirals, and perfusable branched/linear vessels. Successful fabrication of vascularized liver and skeletal muscle tissue constructs show albumin secretion and bundled muscle mimic fibers, respectively. The interconnected microporous networks of colloidal gels result in maintaining printed complex geometries while enabling rapid cell infiltration, in vivo.
KW - 3D bioprinting
KW - colloidal hydrogels
KW - compartmentalized bioprinting
KW - multimaterial extrusion bioprinting
KW - vascular scaffolds
KW - 2023 OA procedure
UR - http://www.scopus.com/inward/record.url?scp=85141979121&partnerID=8YFLogxK
U2 - 10.1021/acsami.2c12585
DO - 10.1021/acsami.2c12585
M3 - Article
C2 - 36346873
AN - SCOPUS:85141979121
SN - 1944-8244
VL - 14
SP - 51602
EP - 51618
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 46
ER -