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Synthesis and screening of N-acyl thiolated chitosans for antibacterial applications

机译:抗菌应用N-酰基硫醇壳聚糖的合成及筛选

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摘要

Low-molecular weight chitosan-thioglycolic acid has shown significant antibacterial properties against different microorganisms. In order to explore the potential and structure-activity relationships of newly synthesized alkyl thiomers, chitosan has been functionalized with a series of thio-acids with increasing alkyl chain length. All thiomers were characterized with special emphasis on the determination of their degree of deacetylation and substitution, as well as on their molecular weight and amount of thiol groups. The pre-screened chitosan-thiomers were further investigated with plate counting on Pseudomonas aeruginosa, Streptococcus sobrinus and Streptococcus mutans. Furthermore, LIVE/DEAD assays supported the efficiency of chitosan-thiomers against the above microorganisms. All fully characterized chitosan-thiomers showed comparable or enhanced antimicrobial activity compared to pristine chitosan. Our comprehensive approach paves the way to detailed explorations of much sought-after structure activity relationships in the complex chitosan parameter room, starting from correlations between alkyl chain length and antimicrobial activity.
机译:低分子量壳聚糖 - 硫代乙酰吡啶酸对不同微生物的显着抗菌性能显示出显着的抗菌性质。为了探讨新合成的烷基硫聚物的潜在和结构 - 活性关系,壳聚糖已用一系列硫酸碳酸官能团官能化,随着烷基链长度的增加。所有巯基的特征在于特别强调测定其脱乙酰化和取代度,以及它们的分子量和硫醇基的量。进一步研究预筛选的壳聚糖巯基,用铜绿假单胞菌,链球菌和链球菌异常计数。此外,活/死导支持壳聚糖 - 巯基的效率对上述微生物。与原始壳聚糖相比,所有完全表征的壳聚糖晶体表现出可比或增强的抗菌活性。我们的综合方法铺设了在复杂的壳聚糖参数室中大量寻求的结构活动关系的详细探索,从烷基链长度与抗微生物活性之间的相关性开始。

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