| Literature DB >> 31430428 |
Xu Yan1, Wei-Wei Fang1, Jingzhe Xue2, Tian-Ci Sun1, Liang Dong2, Zhengbao Zha3, Haisheng Qian3, Yong-Hong Song1, Min Zhang4, Xinglong Gong2, Yang Lu1, Tao He1.
Abstract
An in situ forming hydrogel has emerged as a promising wound dressing recently. As physically cross-linked hydrogels are normally unstable, most in situ forming hydrogels are chemically cross-linked. However, big concerns have remained regarding the slow gelation and the potential toxicity of residual functional groups from cross-linkers or the polymer matrix. Herein, we report a sprayable in situ forming hydrogel composed of poly(N-isopropylacrylamide166-co-n-butyl acrylate9)-poly(ethylene glycol)-poly(N-isopropylacrylamide166-co-n-butyl acrylate9) copolymer (P(NIPAM166-co-nBA9)-PEG-P(NIPAM166-co-nBA9), denoted as PEP) and silver-nanoparticles-decorated reduced graphene oxide nanosheets (Ag@rGO, denoted as AG) in response to skin temperature. This thermoresponsive hydrogel exhibits intriguing sol-gel irreversibility at low temperatures for the stable dressing of a wound, which is attributed to the inorganic/polymeric dual network and abundant coordination interactions between Ag@rGO nanosheets and PNIPAM. The biocompatibility and antibacterial ability against methicillin-resistant Staphylococcus aureus (MRSA) of this PEP-AG hydrogel wound dressing are confirmed in vitro and in vivo, which could transparently promote the healing of a MRSA-infected skin defect.Entities:
Keywords: hydrogel; in situ forming; irreversibility; methicillin-resistant Staphylococcus aureus; sol−gel transition; thermoresponsive; wound closure
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Year: 2019 PMID: 31430428 DOI: 10.1021/acsnano.9b02845
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881