Free radical polymerization is a mature method and can be used for preparing multifunctional hydrogels by simply changing the commercial monomers, but the harsh and timeconsuming initiation conditions restrict its injectable ability, which further limits its application in the biomedical field. Though some catalysts can be used to accelerate the polymerization, their application is restrained by the biotoxicity. Hence, finding a biocompatible catalyzer for in situ free radical polymerization of hydrogels has a great prospect in biomedical application but is still challenging. In this study, we discovered that silver ions could catalyze free radical polymerization under ambient by transforming hydrone into hydroxyl radicals in the presence of ammonium persulfate, and the in situ-formed hydrogels prepared by this way showed great histocompatibility, hemocompatibility, cytocompatibility, and immunocompatibility. Benefitting from its convenience and biocompatibility, the in situ polymerization of polyacrylamide-based hydrogels for tissue adhesion, wound dressing, and conductive materials on the skin could be realized by simply blending diverse ingredients. Furthermore, this discovery may be a step toward the in situ-polymerized hydrogels for biomedical applications.

A bioinspired strategy via self-sacrificing micro-reactors is proposed to prepare hydrogel spheres with ultrahigh adsorption capability within 150 seconds.

Brand new Kevlar/GO composite gel beads assembled by π–π interaction serve as safe and self-anticoagulant absorbents in hemoperfusion fields.

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