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The aim of the present work was to prepare a well-defined hydrogel of chemically cross-linked and organ-metallic complexed interpenetrating PEG networks. The hydrogel was synthesized via the reaction of copper(I)- catalyzed 1,3-dipolar azide-alkyne cycloaddition(CuA AC) with poly(ethylene glycol)-dopamine(PEG-DA)(“Click Chemistry”) followed by complexation with Fe~(3+) ions to crosslink the polymeric network. The chemical composition and morphology of the resulting hydrogels were characterized by Fourier transform infrared spectroscopy(FTIR), ~1H-NMR and scanning electron microscopy(SEM). Swelling ratio, mechanical strength, conductivity, and degradation behaviors of the hydrogels were also studied. The effect of the polymer chain length on properties of hydrogels was explored. The compressive strength of hydrogels could reach as high as 13.1 MPa with a conductivity of 2.2 × 10~(-5) S·cm~(-1). The hydrogels also exhibited excellent thermal stability even at a temperature of 300 °C, whereas degradation of the hydrogel after 7 weeks was observed under a physiological condition. In addition, the hydrogel exhibited a good biocompatibility based on its in vivo performance through an in vivo subcutaneous implantation model. No inflammation and no obvious abnormality of the surrounding tissue were observed when the hydrogel was subcutaneously implanted for 2 weeks. This work is a step towards creating a new pathway to synthesize hydrogels of interpenetrating networks which could be of important applications in the future research.
The aim of the present work was to prepare a well-defined hydrogel of chemically cross-linked and organ-metallic complexed interpenetrating PEG networks. The hydrogel was synthesized via the reaction of copper (I) - catalyzed 1,3-dipolar azide-alkyne The chemical composition and morphology of the cycloaddition (CuA AC) with poly (ethylene glycol) -dopamine (PEG-DA) (“Click Chemistry ”) followed by complexation with Fe ~ (3+) ions to crosslink the polymeric network resulting hydrogels were characterized by Fourier transform infrared spectroscopy (FTIR), ~ 1H-NMR and scanning electron microscopy (SEM). Swelling ratio, mechanical strength, conductivity, and degradation behaviors of the hydrogels were also studied. The effect of the polymer chain length The hydrogels also exhibited excellent thermal stability even at a. The compressive strength of hydrogels could reach as high as 13.1 MPa with a conductivity of 2.2 × 10 -5 S · cm -1. temperature of 300 ° C , while degradation of the hydrogel after 7 weeks was observed under a physiological condition. In addition, the hydrogel exhibited a good biocompatibility based on its in vivo performance through an in vivo subcutaneous implantation model. No inflammation and no obvious abnormality of the surrounding tissue were observed when the hydrogel was subcutaneously implanted for 2 weeks. This work is a step towards creating a new pathway to synthesize hydrogels of interpenetrating networks which could be of important applications in the future research.