Light-cured conductive hydrogels have attracted immense
interest
in the regeneration of electroactive tissues and bioelectronic interfaces.
Despite the unique properties of MXene (MX), its light-blocking effect
in the range of 300–600 nm hinders the efficient cross-linking
of photocurable hydrogels. In this study, we investigated the photo-cross-linking
process of MX-gelatin methacrylate (GelMa) composites with different
types of photoinitiators and MX concentrations to prepare biocompatible,
injectable, conductive, and photocurable composite hydrogels. The
examined photoinitiators were Eosin Y, Irgacure 2959 (Type I), and
lithium phenyl-2,4,6-trimethylbenzoyl phosphinate (Type II). The light-blocking
effect of MX strongly affected the thickness, pore structure, swelling
ratio, degradation, and mechanical properties of the light-cured hydrogels.
Uniform distribution of MX in the hydrogel matrix was achieved at
concentrations up to 0.04 wt % but the film thickness and curing times
varied depending on the type of photoinitiator. It was feasible to
prepare thin films (0.5 mm) by employing Type I photoinitiators under
a relatively long light irradiation (4–5 min) while thick films
with centimeter sizes could be rapidly cured by using Type II photoinitiator
(<60 s). The mechanical properties, including elastic modulus,
toughness, and stress to break for the Type II hydrogels were significantly
superior (up to 300%) to those of Type I hydrogels depending on the
MX concentration. The swelling ratio was also remarkably higher (648–1274%).
A conductivity of about 1 mS/cm was attained at 0.1 mg/mL MX for the
composite hydrogel cured by the Type I photoinitiator. In vitro cytocompatibility
assays determined that the hydrogels promoted cell viability, metabolic
activity, and robust proliferation of C2C12 myoblasts, which indicated
their potential to support muscle cell growth during myogenesis. The
developed photocurable GelMa-MX hydrogels have the potential to serve
as bioactive and conductive scaffolds to modulate cellular functions
and for tissue-device interfacing.