4.8 Article

Tunable and Compartmentalized Multimaterial Bioprinting for Complex Living Tissue Constructs

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 14, 期 46, 页码 51602-51618

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c12585

关键词

compartmentalized bioprinting; 3D bioprinting; multimaterial extrusion bioprinting; vascular scaffolds; colloidal hydrogels

资金

  1. National Institutes of Health [R01AR077132, R01AR074234, R21EB026824, R01AR073822]
  2. AHA Innovative Project Award [19IPLOI34660079]
  3. Gillian Reny Stepping Strong Center for Trauma Innovation
  4. Brigham Research Institute Innovation Evergreen Fund (IEF) at Brigham and Women's Hospital
  5. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [NRF-2021R1A6A3A14039720]
  6. Dutch Research Council (NWO) [019.183EN.017]

向作者/读者索取更多资源

A combinational multimaterial and embedded bioprinting approach is used to develop implantable constructs that can maintain their structure in vivo. Self-healing and biodegradable colloidal gels are introduced as support baths to improve printing fidelity and provide suitable microenvironments for cell growth and infiltration.
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. Multicompart-ment 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.

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