In situ injectable hydrogels,which have great potential in tissue engineering,are characterized by simple preparation,minimal invasiveness and adaptation to complex shapes.However,injectable hydrogels have higher requirements for biocompatibility and safety due to their use in vivo implantation.Therefore,in this study,a human-like collagen (HLC)-based in situ gel-forming injectable HLC-HPA hydrogel was synthesized by combining the amino group of HLC with the carboxyl group of HPA activated using 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS),followed by crosslinking by horseradish peroxidase (HRP) and H2O2,and used as scaffold material for tissue engineering.The hydrogel stiffness,gel time and biodegradation rate could be easily and independently adjusted by varying the H2O2 and HRP concentrations.Scanning electron microscope (SEM) clarified the homogeneous porous and interconnected internal structures of the hydrogel.In vitro cell viability and in vivo degradation experiments confirmed that the HLC-HPA hydrogel had good biodegradability and excellent biocompatibility.Interestingly,in cultured macrophages,the HLC-HPA hydrogel showed anti-inflammatory activity by reducing the amount of the pro-inflammatory cytokines tumor necrosis factor-α (TNF-α) and interleukin6 (IL-6) and increasing the secretion of the anti-inflammatory cytokine interleukin-10 (IL-10) induced by lipopolysaccharide (LPS).Meanwhile,in animal experiments,HLC-HPA hydrogels exhibit excellent biocompatibility and have properties of hemostasis and reduction of inflammatory response.Therefore,the HLC-HPA hydrogel prepared in this study has great potential for development for use in the biomedical field.