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基于壳聚糖的源自乙酰基三唑基尿嘧啶的席夫碱聚合物:合成、表征、抗菌和抗氧化活性评估以及密度泛函理论计算

Chitosan-based Schiff base polymer derived from acetyl triazolyl uracil: Synthesis, characterization, evaluation of antimicrobial and antioxidant activities, and density functional theory calculations.

作者信息

Abdalla Taghreed Hassan, Ibrahim Ahmed G, Elabbady Samia, Nassar Ekhlass, Hamed Ahmed A, Aboelnaga Asmaa

机构信息

Chemistry Department, Faculty of Women of Arts, Science and Education, Ain Shams University, Heliopolis 11757, Egypt.

Department of Chemistry, Faculty of Science (Boys), Al-Azhar University, Nasr City 11884, Cairo, Egypt.

出版信息

Int J Biol Macromol. 2025 Apr;300:140327. doi: 10.1016/j.ijbiomac.2025.140327. Epub 2025 Jan 27.

Abstract

This work aimed to synthesize a new acetyl triazolyl uracil (UT) compound and subsequently utilize it to obtain a new chitosan-based Schiff base polymer (CH-UT). The new derivative was characterized using elemental analysis, FTIR, H NMR, XRD, TGA, DSC, and SEM analyses. Both UT and CH-UT were evaluated for their antibacterial activities against various Gram-positive and Gram-negative bacteria. The results demonstrated that the CH-UT displayed significant antibacterial activity against E. coli and L. monocytogenes, with inhibition ability of 44 % and 53 %, respectively, and low minimum inhibitory concentration (MIC) values of 31 μg/mL for E. coli and 15 μg/mL for L. monocytogenes. Additionally, the biofilm inhibitory activity showed that chitosan alone reduced E. coli biofilms by 10.25 %, whereas the combination of chitosan with UT in CH-UT increased inhibition to 43.00 %. The maximum biofilm inhibition for S. aureus was 42.02 % with UT alone, surpassing both chitosan and CH-UT. Furthermore, the CH-UT derivative showed notable antioxidant activity, with a value of 72.76 %. Results from frontier molecular orbitals (FMOs) analysis indicated that CH-UT exhibits higher reactivity due to its lower HOMO-LUMO energy gap and modified structure. The triazole group in CH-UT contributes to its potential antibacterial activity through hydrogen bonding and electronic properties.

摘要

本研究旨在合成一种新型乙酰基三唑基尿嘧啶(UT)化合物,并随后利用它制备一种新型壳聚糖基席夫碱聚合物(CH-UT)。采用元素分析、傅里叶变换红外光谱(FTIR)、核磁共振氢谱(H NMR)、X射线衍射(XRD)、热重分析(TGA)、差示扫描量热法(DSC)和扫描电子显微镜(SEM)分析对该新型衍生物进行了表征。对UT和CH-UT针对各种革兰氏阳性菌和革兰氏阴性菌的抗菌活性进行了评估。结果表明,CH-UT对大肠杆菌和单核细胞增生李斯特菌显示出显著的抗菌活性,抑制能力分别为44%和53%,对大肠杆菌的最低抑菌浓度(MIC)值低至31μg/mL,对单核细胞增生李斯特菌的MIC值为15μg/mL。此外,生物膜抑制活性表明,单独的壳聚糖可使大肠杆菌生物膜减少10.25%,而壳聚糖与UT在CH-UT中的组合使抑制率提高到43.00%。单独使用UT时,对金黄色葡萄球菌的最大生物膜抑制率为42.02%,超过了壳聚糖和CH-UT。此外,CH-UT衍生物显示出显著的抗氧化活性,值为72.76%。前沿分子轨道(FMO)分析结果表明,CH-UT由于其较低的最高占据分子轨道(HOMO)-最低未占据分子轨道(LUMO)能隙和改性结构而表现出更高的反应活性。CH-UT中的三唑基团通过氢键和电子性质对其潜在的抗菌活性有贡献。

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