壳聚糖
抗菌剂
溶解度
结晶度
抗菌活性
伤口愈合
化学
核化学
细菌
有机化学
外科
医学
生物
结晶学
遗传学
作者
Qifeng Dang,Kai Liu,Chengsheng Liu,Tao Xu,Jingquan Yan,Feilong Yan,Dongsu Cha,Qianqian Zhang,Yachan Cao
标识
DOI:10.1016/j.carbpol.2017.10.019
摘要
This work aims to prepare 3,6-O-N-acetylethylenediamine modified chitosan (AEDMCS) and evaluate its potential use as an antimicrobial wound dressing material. UV, FTIR, and 1H NMR results demonstrated N-acetylethylenediamine groups were successfully grafted to C3OH and C6OH on polysaccharide skeletons. TGA, XRD, and solubility tests indicated that as compared with chitosan, AEDMCS had diminished thermostability, decreased crystallinity, and greatly improved solubility. AEDMCS, with degrees of deacetylation and substitution being respectively 90.3% and 0.72, exhibited higher antibacterial activity than chitosan against six bacteria generally causing wound infections. Meanwhile, AEDMCS had permissible hemolysis and cytotoxicity and low BSA adsorption even at a AEDMCS concentration of 25mg/mL. Acute toxicity tests showed AEDMCS was nontoxic. Moreover, the wound healing property was preliminarily evaluated, illustrating that AEDMCS enhanced wound healing rates as expected and had no significant differences as compared with chitosan. These results suggested AEDMCS might be a potential material used as antibacterial wound dressings.
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