Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5156350 | Carbohydrate Polymers | 2018 | 42 Pages |
Abstract
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 25Â mg/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.
Keywords
MTT (PubChem CID: 64965)Chitin (PubChem CID: 6857375)Ethylenediamine (PubChem CID: 3301)Monochloroacetic acid (PubChem CID: 300)Ethanol (PubChem CID: 702)Acetic acid (PubChem CID: 176)Isopropanol (PubChem CID: 3776)CharacterizationBiocompatibilitySodium dodecyl sulfate (PubChem CID: 3423265)Antibacterial activityChitosan derivativeSodium hydroxide (PubChem CID: 14798)
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Qifeng Dang, Kai Liu, Chengsheng Liu, Tao Xu, Jingquan Yan, Feilong Yan, Dongsu Cha, Qianqian Zhang, Yachan Cao,