There is a growing
need to develop novel well-characterized biological
inks (bioinks) that are customizable for three-dimensional (3D) bioprinting
of specific tissue types. Gelatin methacryloyl (GelMA) is one such
candidate bioink due to its biocompatibility and tunable mechanical
properties. Currently, only low-concentration GelMA hydrogels (≤5%
w/v) are suitable as cell-laden bioinks, allowing high cell viability,
elongation, and migration. Yet, they offer poor printability. Herein,
we optimize GelMA bioinks in terms of concentration and cross-linking
time for improved skeletal muscle C2C12 cell spreading in 3D, and
we augment these by adding gold nanoparticles (AuNPs) or a two-dimensional
(2D) transition metal carbide (MXene nanosheets) for enhanced printability
and biological properties. AuNP and MXene addition endowed GelMA with
increased conductivity (up to 0.8 ± 0.07 and 0.9 ± 0.12
S/m, respectively, compared to 0.3 ± 0.06 S/m for pure GelMA).
Furthermore, it resulted in an improvement of rheological properties
and printability, specifically at 10 °C. Improvements in electrical
and rheological properties led to enhanced differentiation of encapsulated
myoblasts and allowed for printing highly viable (97%) stable constructs.
Taken together, these results constitute a significant step toward
fabrication of 3D conductive tissue constructs with physiological
relevance.