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高荧光π共轭偶氮甲碱和二价金属配合物作为抗菌和抗生物膜候选物

Highly Fluorescent π-Conjugated Azomethines and Divalent Metal Complexes as Antibacterial and Antibiofilm Nominees.

作者信息

Baydeniz Şeyma Nur Ural, Uçan Halil İsmet, Sevgi Fatih, Obalı İhsan, Yılmaz Obalı Aslıhan

机构信息

Department of Chemistry, Science Faculty, Selcuk University, Konya, Türkiye.

Department of Medical Services and Techniques, Vocational School of Health Services, Selcuk University, Konya, Türkiye.

出版信息

J Fluoresc. 2024 Jul 30. doi: 10.1007/s10895-024-03855-x.

Abstract

π-Conjugated azomethine ligands differing in the naphthalene or phenylmethane-centered core structure and their divalent cobalt, nickel, copper, and zinc metal complexes were prepared and well-characterized by spectral analyses in solid state. Magnetic natures of the complexes were determined by magnetic susceptibility measurements in solid-state. Their remarkable photophysical characteristics were recorded by Uv-vis and Fluorescence spectroscopic techniques. At their excitation wavelenght of 265 nm, all molecules exhibited triple fluorescence emission bands with promising intensities above 673 nm in near infra-red region. Antibacterial and antibiofilm activities of the π-conjugated azomethines are promising for potential applications in medical and healthcare settings. Hence, the antibacterial/antibiofilm activity of the π-conjugated azomethine ligands and their metal complexes against some clinically important bacteria namely Staphylococcus aureus (MSSA), Methicillin-resistant Staphylococcus aureus (MRSA), Staphylococcus epidermidis, Escherichia coli, Pseudomonas aeruginosa and Proteus mirabilis was investigated, and the obtained results have shown that the ligands and complexes had a remarkable antibacterial effect, especially on Proteus mirabilis. Metal complexes have been found to have a significant inhibitory effect on biofilm formation by MRSA, MSSA, and P. mirabilis compared to ligands. The copper (II) complex of ligand-2 showed the highest inhibition percentage, significantly reducing biofilm formation for MRSA and MSSA. Furthermore, cobalt (II) complexes of the ligands selectively inhibited the growth of the opportunistic pathogen P. mirabilis biofilms, indicating that metal complexes might be a good choice for future antibiofilm studies.

摘要

制备了以萘或苯甲烷为中心核心结构的π共轭偶氮甲碱配体及其二价钴、镍、铜和锌金属配合物,并通过固态光谱分析对其进行了充分表征。通过固态磁化率测量确定了配合物的磁性性质。通过紫外可见光谱和荧光光谱技术记录了它们显著的光物理特性。在265nm的激发波长下所有分子在近红外区域673nm以上均表现出具有良好强度的三重荧光发射带。π共轭偶氮甲碱的抗菌和抗生物膜活性在医学和医疗保健领域具有潜在应用前景。因此,研究了π共轭偶氮甲碱配体及其金属配合物对一些临床重要细菌即金黄色葡萄球菌(MSSA)、耐甲氧西林金黄色葡萄球菌(MRSA)、表皮葡萄球菌、大肠杆菌、铜绿假单胞菌和奇异变形杆菌的抗菌/抗生物膜活性,所得结果表明配体和配合物具有显著的抗菌作用,尤其是对奇异变形杆菌。已发现金属配合物与配体相比对MRSA、MSSA和奇异变形杆菌的生物膜形成具有显著抑制作用。配体-2的铜(II)配合物显示出最高的抑制率,显著减少了MRSA和MSSA的生物膜形成。此外,配体的钴(II)配合物选择性地抑制了机会性病原体奇异变形杆菌生物膜的生长,这表明金属配合物可能是未来抗生物膜研究的一个不错选择。

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