4.8 Article

Digital Assembly of Spherical Viscoelastic Bio-Ink Particles

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 32, Issue 6, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202109004

Keywords

human islets; insulin release; multiscale porosity; viscoelastic bio-ink particles; voxelated bioprinting

Funding

  1. UVA Center for Advanced Biomanufacturing
  2. NSF CAREER [DMR-1944625]
  3. ACS PRF [6132047-DNI]
  4. UVA LaunchPad for Diabetes
  5. Virginia's Commonwealth Health Research Board

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A voxelated bioprinting technique, DASP, has been developed for the digital assembly of spherical particles, enabling the generation and assembly of bio-ink droplets. Using DASP, mechanically robust porous scaffolds have been created for encapsulating human pancreatic islets to achieve sustained insulin release. The study shows the potential for engineering tissue constructs with highly heterogeneous yet tightly organized structures for therapeutic applications.
3D bioprinting additively assembles bio-inks to manufacture tissue-mimicking biological constructs, but with the typical building blocks limited to 1D filaments. Here, it is developed a voxelated bioprinting technique for the digital assembly of spherical particles (DASP), which are effectively 0D voxels-the basic unit of 3D structures. It is shown that DASP enables on-demand generation, deposition, and assembly of viscoelastic bio-ink droplets. A two-parameter diagram is developed to outline the viscoelasticity of bio-inks required for printing spherical particles of good fidelity. Moreover, a strategy is developed for engineering bio-inks with independently controllable viscoelasticity and mesh size, two of the most important yet intrinsically coupled physical properties of biomaterials. Using DASP, mechanically robust, multiscale porous scaffolds composed of interconnected yet distinguishable hydrogel particles are created. Finally, it is demonstrated the application of the scaffolds in encapsulating human pancreatic islets for sustained responsive insulin release. Together with the knowledge of bio-ink design, DASP might be used to engineer highly heterogeneous, yet tightly organized tissue constructs for therapeutic applications.

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