Literature DB >> 32070523

Preparation of 2,6-diurea-chitosan oligosaccharide derivatives for efficient antifungal and antioxidant activities.

Jingjing Zhang1, Xueqi Sun1, Yuan Chen1, Yingqi Mi1, Wenqiang Tan2, Qin Miao2, Qing Li2, Fang Dong2, Zhanyong Guo3.   

Abstract

In this study, 2-urea-chitosan oligosaccharide derivatives (2-urea-COS derivatives) and 2,6-diurea-chitosan oligosaccharide derivatives (2,6-diurea-COS derivatives) were successfully designed and synthesized via intermediate 2-methoxyformylated chitosan oligosaccharide. All samples were characterized and compared based on FT-IR, 1H NMR spectroscopy, and elemental analysis. The antifungal effects of COS derivatives were tested against Fusarium oxysporum f. sp. niveum, Phomopsis asparagus, and Botrytis cinereal. Their antioxidant properties, including superoxide radicals' scavenging activity, hydroxyl radicals' scavenging activity, and DPPH radicals' scavenging activity were also explored within different concentrations. COS derivatives bearing urea groups showed improved bioactivity compared with pristine COS and 2,6-diurea-COS derivatives had a higher biological activity than 2-urea-COS derivatives in tested concentrations. Additionally, L929 cells were used to carry out cytotoxicity test of COS and COS derivatives by CCK-8 assay. The results indicated that some of samples showed low cytotoxicity. These findings offered a suggestion that COS derivatives bearing urea groups are promising biological materials.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Antifungal activity; Antioxidant activity; Chitosan oligosaccharide derivatives; Cytotoxicity; Urea groups

Year:  2020        PMID: 32070523     DOI: 10.1016/j.carbpol.2020.115903

Source DB:  PubMed          Journal:  Carbohydr Polym        ISSN: 0144-8617            Impact factor:   9.381


  4 in total

1.  [Islet biomimetic microenvironment constructed by chitosan oligosaccharide protects islets from hypoxia-induced damage by reducing intracellular reactive oxygen species].

Authors:  Dongzhi Wang; Yibing Guo; Yan Huang; Biwen Zhu; Haopeng Pan; Zhiwei Wang
Journal:  Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi       Date:  2022-05-15

2.  Synthesis of Hydroxypropyltrimethyl Ammonium Chitosan Derivatives Bearing Thioctate and the Potential for Antioxidant Application.

Authors:  Wenqiang Tan; Conghao Lin; Jingjing Zhang; Qing Li; Zhanyong Guo
Journal:  Molecules       Date:  2022-04-21       Impact factor: 4.927

3.  A temperature-induced chitosanase bacterial cell-surface display system for the efficient production of chitooligosaccharides.

Authors:  Qianqian Li; Tuantuan Wang; Yangzhi Ye; Shimin Guan; Baoguo Cai; Shuo Zhang; Shaofeng Rong
Journal:  Biotechnol Lett       Date:  2021-05-16       Impact factor: 2.461

Review 4.  The Microstructure, Antibacterial and Antitumor Activities of Chitosan Oligosaccharides and Derivatives.

Authors:  Dawei Yu; Jiayao Feng; Huimin You; Shipeng Zhou; Yan Bai; Jincan He; Hua Cao; Qishi Che; Jiao Guo; Zhengquan Su
Journal:  Mar Drugs       Date:  2022-01-13       Impact factor: 5.118

  4 in total

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