生物相容性
抗菌活性
细菌纤维素
嫁接
氯乙烯
纤维素
化学
聚合物
聚合
表面改性
氯化铵
甲壳素
铵
高分子化学
化学工程
核化学
壳聚糖
有机化学
共聚物
细菌
物理化学
工程类
生物
遗传学
作者
Haiyan Liu,Yang Hu,Yongjun Zhu,Xiuping Wu,Xin Zhou,Haobo Pan,Shu Chen,Pengfei Tian
标识
DOI:10.1016/j.ijbiomac.2019.12.052
摘要
Bacterial cellulose (BC) is a biosynthesized carbohydrate polymer with excellent biocompatibility and water holding capability. However, it lacks an inherent antibacterial activity that has limited its in-depth biomedical applications. This study investigated a novel strategy of adopting a simultaneous process to chemically anchor a quaternary ammonium salt (R-N(CH3)+) with a special vinyl group (2-methacryloyloxyethyl trimethylammonium chloride, METAC) onto the BC, and meanwhile, enhance the density of (R-N(CH3)+) via free radical vinyl polymerization. The results have confirmed the transition of BC surface from a negatively-charged surface to a polycationic surface via such a simultaneous reaction. As compared to chitin film (a representative of R-NH3+), the resulting METAC-grafted BC (a representative of high-density R- N(CH3)+) acquired excellent water absorbability (40 times of dry weight of the BC), 99% antibacterial activity against Escherichia coli and Staphylococcus aureus, a satisfactory in-vitro biocompatibility, and a better in-vivo wound healing outcome with an excellent in-vivo antibacterial efficacy. This study has exhibited potential in utilizing a facile method to prepare a bio-safe, adaptive antibacterial surface for various biomedical applications.
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