Effect of the structure of chitosan quaternary ammonium salts with different spacer groups on antibacterial and antibiofilm activities

IF 8.5 1区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
{"title":"Effect of the structure of chitosan quaternary ammonium salts with different spacer groups on antibacterial and antibiofilm activities","authors":"","doi":"10.1016/j.ijbiomac.2024.133777","DOIUrl":null,"url":null,"abstract":"<div><p>In this study, three types of dodecyl chitosan quaternary ammonium salts, each with different spacer groups were synthesized. These chitosan derivatives are <em>N′</em>,<em>N′</em>-dimethyl-<em>N′-</em>dodecyl-ammonium chloride-<em>N</em>-amino-acetyl chitosan (DMDAC), <em>N′-</em>dodecyl-<em>N</em>-isonicotinyl chitosan chloride (DINCC) and <em>N′</em>,<em>N′</em>-dimethyl-<em>N′-</em>dodecyl-ammonium chloride-<em>N</em>-benzoyl chitosan (DMDBC). The synthesized products were characterized using Fourier transform infrared spectrometers, nuclear magnetic resonance, thermogravimetric analysis, and elemental analysis. The antibacterial and antibiofilm activities against <em>Escherichia coli</em> (<em>E. coli</em>) and <em>Staphylococcus aureus</em> (<em>S. aureus</em>) were investigated. The experimental results indicated that the introduction of hydrophobic groups of spacer groups could enhance the antibacterial and antibiofilm activities of the chitosan derivatives. The antibacterial rates of the chitosan derivatives were over 90 % for both <em>E. coli</em> and <em>S. aureus</em> at a concentration of 0.5 mg/mL. The chitosan derivatives removed &gt;50 % of the mature biofilm of <em>E. coli</em> and over 90 % of the mature biofilm of <em>S. aureus</em> at a concentration of 2.5 mg/mL. Further, the synthesized chitosan derivatives were determined to be non-toxic to L929 cells. Among them, DMDBC exhibited the most promising overall performance and show potential for wide-ranging applications in food preservation, disinfectants, medical, and other fields.</p></div>","PeriodicalId":333,"journal":{"name":"International Journal of Biological Macromolecules","volume":"276 ","pages":"Article 133777"},"PeriodicalIF":8.5000,"publicationDate":"2024-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Biological Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0141813024045823","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

In this study, three types of dodecyl chitosan quaternary ammonium salts, each with different spacer groups were synthesized. These chitosan derivatives are N′,N′-dimethyl-N′-dodecyl-ammonium chloride-N-amino-acetyl chitosan (DMDAC), N′-dodecyl-N-isonicotinyl chitosan chloride (DINCC) and N′,N′-dimethyl-N′-dodecyl-ammonium chloride-N-benzoyl chitosan (DMDBC). The synthesized products were characterized using Fourier transform infrared spectrometers, nuclear magnetic resonance, thermogravimetric analysis, and elemental analysis. The antibacterial and antibiofilm activities against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) were investigated. The experimental results indicated that the introduction of hydrophobic groups of spacer groups could enhance the antibacterial and antibiofilm activities of the chitosan derivatives. The antibacterial rates of the chitosan derivatives were over 90 % for both E. coli and S. aureus at a concentration of 0.5 mg/mL. The chitosan derivatives removed >50 % of the mature biofilm of E. coli and over 90 % of the mature biofilm of S. aureus at a concentration of 2.5 mg/mL. Further, the synthesized chitosan derivatives were determined to be non-toxic to L929 cells. Among them, DMDBC exhibited the most promising overall performance and show potential for wide-ranging applications in food preservation, disinfectants, medical, and other fields.

具有不同间隔基团的壳聚糖季铵盐结构对抗菌和抗生物膜活性的影响
本研究合成了三种十二烷基壳聚糖季铵盐,每种季铵盐都带有不同的间隔基团。这些壳聚糖衍生物分别是 N',N'-二甲基-N'-十二烷基氯化铵-N-氨基乙酰壳聚糖(DMDAC)、N'-十二烷基-N-异烟酸基壳聚糖氯化物(DINCC)和 N',N'-二甲基-N'-十二烷基氯化铵-N-苯甲酰基壳聚糖(DMDBC)。利用傅立叶变换红外光谱仪、核磁共振、热重分析和元素分析对合成产品进行了表征。对大肠杆菌(E. coli)和金黄色葡萄球菌(S. aureus)的抗菌和抗生物膜活性进行了研究。实验结果表明,引入疏水基团的间隔基团可增强壳聚糖衍生物的抗菌和抗生物膜活性。浓度为 0.5 毫克/毫升时,壳聚糖衍生物对大肠杆菌和金黄色葡萄球菌的抗菌率均超过 90%。在 2.5 毫克/毫升的浓度下,壳聚糖衍生物可去除超过 50% 的大肠杆菌成熟生物膜和超过 90% 的金黄色葡萄球菌成熟生物膜。此外,经测定,合成的壳聚糖衍生物对 L929 细胞无毒。在这些衍生物中,DMDBC 的整体性能最为突出,有望在食品保鲜、消毒剂、医疗等领域得到广泛应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
International Journal of Biological Macromolecules
International Journal of Biological Macromolecules 生物-生化与分子生物学
CiteScore
13.70
自引率
9.80%
发文量
2728
审稿时长
64 days
期刊介绍: The International Journal of Biological Macromolecules is a well-established international journal dedicated to research on the chemical and biological aspects of natural macromolecules. Focusing on proteins, macromolecular carbohydrates, glycoproteins, proteoglycans, lignins, biological poly-acids, and nucleic acids, the journal presents the latest findings in molecular structure, properties, biological activities, interactions, modifications, and functional properties. Papers must offer new and novel insights, encompassing related model systems, structural conformational studies, theoretical developments, and analytical techniques. Each paper is required to primarily focus on at least one named biological macromolecule, reflected in the title, abstract, and text.
文献相关原料
公司名称
产品信息
索莱宝
Dialysis membranes
阿拉丁
1-chlorododecane
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信