OBTAINING AND INVESTIGATION OF THE BIOLOGICAL ACTIVITY OF GUANIDINE COMPLEXES WITH PECTIN POLYSACCHARIDES

O. R. Akhmedov, S. Shomurotov, Anastasiya Vyacheslavovna Sidorenko, A. Turaev
{"title":"OBTAINING AND INVESTIGATION OF THE BIOLOGICAL ACTIVITY OF GUANIDINE COMPLEXES WITH PECTIN POLYSACCHARIDES","authors":"O. R. Akhmedov, S. Shomurotov, Anastasiya Vyacheslavovna Sidorenko, A. Turaev","doi":"10.14258/jcprm.20230412787","DOIUrl":null,"url":null,"abstract":"Pectin polysaccharides, due to the presence of reactive carboxyl functional groups in the structure, have a high complexing ability. This expands the scope of their practical application for the development of new biologically active substances. In this work, we propose the preparation of complex compounds based on sodium pectate and guanidine hydrochloride. By varying the molar amount of guanidine in relation to the acid groups of the polysaccharide matrix, samples were obtained that differ in the degree of substitution, the content of the amino derivative of the compound, and the inherent viscosity. The optimal ratio of the starting compounds was determined, at which the limiting amount of guanidine is bound to -COO- groups of pectin macromolecules. The structure of the resulting complexes was studied by FTIR spectroscopy. It has been established that the interaction of guanidine with polysaccharide carboxyls is accompanied by a change in the intensity of the absorption bands corresponding to the ionized acid group. Also, the binding of guanidine to the polysaccharide matrix through ionic bonds has been proven by carrying out the hydrolytic cleavage of the complex compound in an acidic medium. It is shown that with an increase in the hydrolysis time from 3 to 24 h, a gradual decrease in the initial degree of substitution of the complex compound is observed. The antimicrobial properties of polymer complexes with different characteristics against Staphylococcus aureus and Escherichia coli were studied.","PeriodicalId":9946,"journal":{"name":"chemistry of plant raw material","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"chemistry of plant raw material","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14258/jcprm.20230412787","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Pectin polysaccharides, due to the presence of reactive carboxyl functional groups in the structure, have a high complexing ability. This expands the scope of their practical application for the development of new biologically active substances. In this work, we propose the preparation of complex compounds based on sodium pectate and guanidine hydrochloride. By varying the molar amount of guanidine in relation to the acid groups of the polysaccharide matrix, samples were obtained that differ in the degree of substitution, the content of the amino derivative of the compound, and the inherent viscosity. The optimal ratio of the starting compounds was determined, at which the limiting amount of guanidine is bound to -COO- groups of pectin macromolecules. The structure of the resulting complexes was studied by FTIR spectroscopy. It has been established that the interaction of guanidine with polysaccharide carboxyls is accompanied by a change in the intensity of the absorption bands corresponding to the ionized acid group. Also, the binding of guanidine to the polysaccharide matrix through ionic bonds has been proven by carrying out the hydrolytic cleavage of the complex compound in an acidic medium. It is shown that with an increase in the hydrolysis time from 3 to 24 h, a gradual decrease in the initial degree of substitution of the complex compound is observed. The antimicrobial properties of polymer complexes with different characteristics against Staphylococcus aureus and Escherichia coli were studied.
获得胍与果胶多糖的复合物并研究其生物活性
果胶多糖由于结构中存在活性羧基官能团,因此具有很强的络合能力。这就扩大了它们在开发新的生物活性物质方面的实际应用范围。在这项工作中,我们提出了基于果胶酸钠和盐酸胍的复合物的制备方法。通过改变胍与多糖基质中酸性基团的摩尔量,我们得到了在取代程度、化合物中氨基衍生物的含量和固有粘度方面各不相同的样品。确定了起始化合物的最佳比例,在此比例下,胍与果胶大分子的 -COO- 基团结合的量达到极限。通过傅立叶变换红外光谱法研究了所得复合物的结构。结果表明,胍与多糖羧基的相互作用伴随着电离酸基相应吸收带强度的变化。此外,通过在酸性介质中对复合物进行水解裂解,证明了胍通过离子键与多糖基质结合。结果表明,随着水解时间从 3 小时增加到 24 小时,复合化合物的初始取代度逐渐降低。研究了具有不同特性的聚合物复合物对金黄色葡萄球菌和大肠杆菌的抗菌特性。
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
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信