4.7 Article

Homogeneous and Reproducible Mixing of Highly Viscous Biomaterial Inks and Cell Suspensions to Create Bioinks

Journal

GELS
Volume 7, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/gels7040227

Keywords

bioprinting; plotting; highly viscous bioink; alginate; methylcellulose; plasma; gellan gum; static mixer

Funding

  1. German Research Foundation (DFG) [LO 1939/3-1]
  2. ministry of Science, Research, and the Arts Baden Wuerttemberg [IP2019]
  3. Paul Hartmann AG
  4. Avina Foundation (Switzerland)

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Highly viscous bioinks are beneficial for three-dimensional fabrication of cell-laden constructs, and a novel method using a mixing unit connecting two syringes has been developed for homogeneous and reproducible mixing of high viscosity biomaterial ink and cell suspension. This method showed improved viability of cells and homogeneity of bioink compared to manual mixing method, providing a reliable comparison of mixing quality.
Highly viscous bioinks offer great advantages for the three-dimensional fabrication of cell-laden constructs by microextrusion printing. However, no standardised method of mixing a high viscosity biomaterial ink and a cell suspension has been established so far, leading to non-reproducible printing results. A novel method for the homogeneous and reproducible mixing of the two components using a mixing unit connecting two syringes is developed and investigated. Several static mixing units, based on established mixing designs, were adapted and their functionality was determined by analysing specific features of the resulting bioink. As a model system, we selected a highly viscous ink consisting of fresh frozen human blood plasma, alginate, and methylcellulose, and a cell suspension containing immortalized human mesenchymal stem cells. This bioink is crosslinked after fabrication. A pre-crosslinked gellan gum-based bioink providing a different extrusion behaviour was introduced to validate the conclusions drawn from the model system. For characterisation, bioink from different zones within the mixing device was analysed by measurement of its viscosity, shape fidelity after printing and visual homogeneity. When taking all three parameters into account, a comprehensive and reliable comparison of the mixing quality was possible. In comparison to the established method of manual mixing inside a beaker using a spatula, a significantly higher proportion of viable cells was detected directly after mixing and plotting for both bioinks when the mixing unit was used. A screw-like mixing unit, termed HighVisc, was found to result in a homogenous bioink after a low number of mixing cycles while achieving high cell viability rates.

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