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This study aimed to investigate the suitability of a photo\u2010crosslinkable tyraminated poly(vinyl alcohol)\u2010gelatin (PVA\u2010GT) polymer network as an injectable platform for tissue engineering and growth factor delivery. Two formulations were developed by varying the concentration of ruthenium\/sodium persulfate (Ru\/SPS), resulting in formulation\u2010specific physical properties with fast (18 days) and slow (36 days) degradation rates. Their injectability was confirmed across a range of needle sizes (14 to 22G), ensuring versatility for multiple applications. Cytokine release from peripheral blood mononuclear cells and THP\u20101 demonstrated no inflammatory response due to residual ruthenium. When injected subcutaneously into a mouse model, the fast\u2010degrading formulation exhibited greater cellular and vascular infiltration compared to the slow\u2010degrading one. 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