Alginate-Based Bioinks for 3D Bioprinting and Fabrication of Anatomically Accurate Bone Grafts

• Published in: Tissue engineering. Part A 2021-09, Vol.27 (17-18), p.1168-1181
• Main Authors: Gonzalez-Fernandez, Tomas, Tenorio, Alejandro J, Campbell, Kevin T, Silva, Eduardo A, Leach, J Kent
• Format: Article
• Language: English
• Subjects: 3-D printers; Alginic acid; Apoptosis; Biocompatibility; Bone marrow; Calcium chloride; Cell culture; Cell survival; Gelatin; Mechanical properties; Mesenchyme; Mineralization; Original; Original Articles; Osteogenesis; Physical properties; Physicochemical properties; Printing; Rheology; Skin & tissue grafts; Stromal cells
• ISSN: 1937-3341; 1937-335X
• DOI: 10.1089/ten.tea.2020.0305

To realize the promise of three-dimensional (3D) bioprinting, it is imperative to develop bioinks that possess the necessary biological and rheological characteristics for printing cell-laden tissue grafts. Alginate is widely used as a bioink because its rheological properties can be modified through precrosslinking or the addition of thickening agents to increase printing resolution. However, modification of alginate's physiochemical characteristics using common crosslinking agents can affect its cytocompatibility. Therefore, we evaluated the printability, physicochemical properties, and osteogenic potential of four common alginate bioinks: alginate-CaCl 2 (alg-CaCl 2 ), alginate-CaSO 4 (alg-CaSO 4 ), alginate-gelatin (alg-gel), and alginate-nanocellulose (alg-ncel) for the 3D bioprinting of anatomically accurate osteogenic grafts. While all bioinks possessed similar viscosity, printing fidelity was lower in the precrosslinked bioinks. When used to print geometrically defined constructs, alg-CaSO 4 and alg-ncel exhibited higher mechanical properties and lower mesh size than those printed with alg-CaCl 2 or alg-gel. The physical properties of these constructs affected the biological performance of encapsulated bone marrow-derived mesenchymal stromal cells (MSCs). Cell-laden constructs printed using alg-CaSO 4 and alg-ncel exhibited greater cell apoptosis and contained fewer living cells 7 days postprinting. In addition, effective cell–matrix interactions were only observed in alg-CaCl 2 printed constructs. When cultured in osteogenic media, MSCs in alg-CaCl 2 constructs exhibited increased osteogenic differentiation compared to the other three bioinks. This bioink was then used to 3D print anatomically accurate cell-laden scaphoid bones that were capable of partial mineralization after 14 days of in vitro culture. These results highlight the importance of bioink properties to modulate cell behavior and the biofabrication of clinically relevant bone tissues.