Polylactic-co-glycolic acid (PLGA) has widely been used as a biodegradable material for three-dimensional (3D) printed scaffolds. However, the lack of surface chemicals and poor wettability limit the application of the polymer. Therefore, we modified the 3D scaffold surface using plasma surface modifications and evaluated its biocompatibility. To introduce amine functional groups on the 3D PLGA scaffold surface, amine plasma-polymerization was performed using 1, 2-diaminocyclohexane (DACH) monomers. Then, Fibroblast Growth Factor (FGF) was immobilized on the amine-functionalized 3D PLGA scaffold surface using a 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and N-hydroxysuccinimide. Human Gingival Fibroblast (HGF-1) cell behaviors were evaluated through cell adhesion, migration, proliferation, and western blot. The results showed that DACH plasma-polymerization provided the amine-functionalized surface which is capable of immobilizing FGF bioactive molecules on the 3D PLGA scaffold. Cell adhesion, proliferation, and migration on plasma surface-modified scaffolds have greatly improved compared to pristine 3D PLGA scaffolds. Notably, FGF-immobilized groups demonstrated the highest proliferation. These results suggest that the FGF-immobilized scaffold surface had a significant effect on accelerating oral gingival cell proliferation. In the future, 3D PLGA scaffolds with surface functionalized by plasma-polymerization and biomolecule immobilization can be used as a good alternative to autogenous soft tissue grafts for damaged soft tissue restoration.
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