| Popis: |
There is a high demand for in vitro intestinal models towards studying intestinal disfunctions, such as gastrointestinal diseases (Crohn's disease, irritable bowel syndrome, colorectal cancer, etc.) which are commonly diagnosed in modern society. In parallel, in vitro models are utilized for the evaluation of novel food supplements and pharmaceuticals in the intestinal micro-environment. Gelatin-based hydrogels can offer appropriate mechanical cues (down to G’ < 10 kPa) and cell interactivity to obtain physiologically relevant soft tissue models. Therefore, the current paper focused on the development of a novel, gelatin-methacryloyl-aminoethyl-methacrylate (gel-MA-AEMA)-based in vitro intestinal model, which also provides sufficient permeability towards nutrients and drugs. Moreover, the effect of the hydrogel morphology on the cell response was assessed by comparing the formation of a functional intestinal cell monolayer on flat hydrogel films versus 3D hydrogel scaffolds maintaining a close morphological resemblance with the intestinal architecture.A gel-MA-AEMA-based biomaterial ink was formulated and processed towards flat hydrogel films, while digital light processing was exploited to replicate the intestinal microarchitecture. The mechanical assessment of the 2D films confirmed physiologically relevant scaffold stiffness (G’ = 3.30±1.07 kPa). To evaluate the permeability of the hydrogels towards a medium size marker molecule (FITC-dextran 4 kg·mol−1), a static diffusion setup was exploited with custom-made adjustable inserts, which evidenced that both the 2D films and 3D constructs exhibited sufficient permeability. Finally, the combination of the hydrogels with a Caco-2/HT29-MTX co-culture evidenced hydrogel biocompatibility, enabling the formation of a functional cell monolayer after 21 days on the 2D hydrogel films, proven by transepithelial electrical resistance measurements and immunohistochemistry, while the 3D hydrogel constructs did not achieve confluency within 35 days. |
