Abstract
Fish collagen is gaining attention as a sustainable biomaterial for three-dimensional (3D) scaffold fabrication in tissue engineering. In this study, a biomimetic, one-pot crosslinking strategy for native fish skin collagen was developed and compared with a conventional periodate oxidation-Schiff base approach using oxidized maltose. Both approaches increased viscosity and thermal stability while preserving native structural features. The oxidized maltose-crosslinked collagen demonstrated Schiff-base crosslinking, and the one-pot crosslinking method produced a covalent bond that was not a Schiff base. Precrosslinked collagens were processed into microgels and incorporated into calcium alginate to yield a shear-recovering, extrudable ink suitable for 3D extrusion printing. The printed scaffolds maintained structural resilience under physiological conditions, exhibited shear-recovery behavior confirmed by rheological analysis, and supported high cell viability. To enhance biofunctionality, vascular endothelial growth factor was conjugated to the 3D scaffolds, which were subsequently seeded with human bone marrow-derived mesenchymal stem cells. Immunofluorescence staining indicated endothelial lineage differentiation, suggesting that this platform may support the development of vascularized 3D tissue constructs. Impact Statement This study presents a one-pot crosslinking approach to enable three-dimensional extrusion printing of a shear-recovery, precrosslinked fish collagen ink design, eliminating the need for postprinting treatments. Functionalization with vascular endothelial growth factor further enhanced the bioactivity of the printed scaffolds by promoting angiogenic response. Collectively, these findings demonstrate a sustainable and biocompatible strategy that broadens the applicability of fish collagen-based inks for vascularized tissue engineering applications.