Scientists develop a method to print stable biological structures; could be applied to printing human organs in future

Scientists have developed a way to print stable biological structures using bio-ink, an advance that may someday lead to printed human organ replacements. [caption id=“attachment_4278925” align=“alignleft” width=“380”] This is a photograph of a 3-D hydrogel construct obtained through drop-on-drop multi-material bioprintinig. Osaka University[/caption] Before any real applications, “bioprinting” still faces many technical challenges. Processing the bio-ink and making it stick to itself and hold the desired printed gel structure have been proving particularly difficult especially in inkjet printing. Few methods currently exist for gluing bio-ink droplets together and these do not work for every kind of cell, motivating new alternative approaches. Building on their previous work, researchers at Osaka University in Japan have now refined an enzyme-driven approach to sticking biological ink droplets together, enabling complex biological structures to be printed. “Printing any kind of tissue structure is a complex process. The bio-ink must have low enough viscosity to flow through the inkjet printer, but also needs to rapidly form a highly viscose gel-like structure when printed,” said Shinji Sakai, from Osaka University. “Our new approach meets these requirements while avoiding sodium alginate. In fact, the polymer we used offers excellent potential for tailoring the scaffold material for specific purposes,” said Sakai, lead author of the study published in the journal Macromolecular Rapid Communications. Currently, sodium alginate is the main gelling agent used for inkjet bioprinting, but has some compatibility problems with certain cell types. The researcher’s new approach is based on hydrogenation mediated by an enzyme, horseradish peroxidase, which can create cross-links between phenyl groups of an added polymer in the presence of the oxidant hydrogen peroxide. Although hydrogen peroxide itself can also damage cells, the researchers carefully tuned the delivery of cells and hydrogen peroxide in separate droplets to limit their contact and keep the cells alive. More than 90 percent of the cells were viable in biological test gels prepared in this way. A number of complex test structures could also be grown from different types of cells. “Advances in induced pluripotent stem cell technologies have made it possible for us to induce stem cells to differentiate in many different ways,” said Makoto Nakamura, from Osaka University. “Now we need new scaffolds so we can print and support these cells to move closer to achieving full 3D printing of functional tissues. Our new approach is highly versatile and should help all groups working to this goal,” Nakamura said.