Your browser doesn't support javascript.
loading
3D Bioprinting using UNIversal Orthogonal Network (UNION) Bioinks.
Hull, Sarah M; Lindsay, Christopher D; Brunel, Lucia G; Shiwarski, Daniel J; Tashman, Joshua W; Roth, Julien G; Myung, David; Feinberg, Adam W; Heilshorn, Sarah C.
Affiliation
  • Hull SM; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
  • Lindsay CD; Department of Materials Science & Engineering, Stanford University, Stanford, CA 94305, USA.
  • Brunel LG; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
  • Shiwarski DJ; Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
  • Tashman JW; Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
  • Roth JG; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, CA 94305, USA.
  • Myung D; Department of Ophthalmology, Stanford University, Stanford, CA 94305, USA.
  • Feinberg AW; Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
  • Heilshorn SC; Department of Materials Science & Engineering, Stanford University, Stanford, CA 94305, USA.
Adv Funct Mater ; 31(7)2021 Feb 10.
Article in En | MEDLINE | ID: mdl-33613150
ABSTRACT
Three-dimensional (3D) bioprinting is a promising technology to produce tissue-like structures, but a lack of diversity in bioinks is a major limitation. Ideally each cell type would be printed in its own customizable bioink. To fulfill this need for a universally applicable bioink strategy, we developed a versatile, bioorthogonal bioink crosslinking mechanism that is cell compatible and works with a range of polymers. We term this family of materials UNIversal, Orthogonal Network (UNION) bioinks. As demonstration of UNION bioink versatility, gelatin, hyaluronic acid (HA), recombinant elastin-like protein (ELP), and polyethylene glycol (PEG) were each used as backbone polymers to create inks with storage moduli spanning 200 to 10,000 Pa. Because UNION bioinks are crosslinked by a common chemistry, multiple materials can be printed together to form a unified, cohesive structure. This approach is compatible with any support bath that enables diffusion of UNION crosslinkers. Both matrix-adherent human corneal mesenchymal stromal cells and non-matrix-adherent human induced pluripotent stem cell-derived neural progenitor spheroids were printed with UNION bioinks. The cells retained high viability and expressed characteristic phenotypic markers after printing. Thus, UNION bioinks are a versatile strategy to expand the toolkit of customizable materials available for 3D bioprinting.
Key words