Biocompatible dual network bovine serum albumin-loaded hydrogel-accelerates wound healing

[Display omitted] •BSA-PCDN hydrogels were prepared by copolymerizing BSA with polymerizable monomers by utilizing the binding ability of albumin to drugs.•BSA-PCDN hydrogel improved the mechanical strength of natural protein hydrogel with a maximum stress of 1.17 MPa.•BSA-PCDN hydrogel has good bio...

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Veröffentlicht in:European polymer journal 2023-02, Vol.185, p.111820, Article 111820
Hauptverfasser: Liu, Dongmei, Zhao, Susu, Jiang, Yujie, Gao, Chuanhui, Wu, Yumin, Liu, Yuetao
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Sprache:eng
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Zusammenfassung:[Display omitted] •BSA-PCDN hydrogels were prepared by copolymerizing BSA with polymerizable monomers by utilizing the binding ability of albumin to drugs.•BSA-PCDN hydrogel improved the mechanical strength of natural protein hydrogel with a maximum stress of 1.17 MPa.•BSA-PCDN hydrogel has good biocompatibility and wound closure performance in mouse skin incision model. Hydrogels with good biocompatibility and the ability to maintain a moist environment at the wound site, as well as good drug-carrying capacity and slow-release properties, can be used as medical materials for wound dressings. Albumin is the primary plasma protein and the physiological carrier of a wide range of compounds, including drugs. To exploit the binding ability of albumin to drugs, we prepared bovine serum albumin-P (Acrylic acid-co-Acrylamide-co-N-Vinylpyrrolidone-co-Hydroxyethyl methacrylate-co-γ-(methacryloyloxy) propyltrimethoxysilane) double network hydrogels by copolymerizing BSA with various easy-to-polymerize monomers. The synthesized double network hydrogels can substantially improve the mechanical strength of natural protein-based hydrogels with a maximum stress of 1.17 MPa. Due to the good biocompatibility and stable drug release properties of BSA, in vitro evaluation in a mouse skin incision model showed that the hydrogels had a high wound closure effect, providing a feasible strategy for rapid skin wound healing.
ISSN:0014-3057
1873-1945
DOI:10.1016/j.eurpolymj.2023.111820