Purti Mishra, Pooja Sethi, Selva Kumar Ramasamy, A. Saini, H. Tuli, Divya Mittal, Aarti Trehan
{"title":"Antibacterial, DNA photocleavage and molecular docking studies of newly prepared Schiff-based macrocyclic complexes","authors":"Purti Mishra, Pooja Sethi, Selva Kumar Ramasamy, A. Saini, H. Tuli, Divya Mittal, Aarti Trehan","doi":"10.15584/ejcem.2024.1.27","DOIUrl":null,"url":null,"abstract":"Introduction and aim. At present, several microbial diseases are prominent and of concern worldwide. The intent of this study was to examine the antibacterial potential of newly synthesized tetradentate macrocyclic complexes against different bacte rial strains. The macrocyclic scaffold has gained attention as a biologically active class of supramolecular chemistry due to its unique properties and ability to target various microorganisms. Thus, the goal of the present study was to develop a series of biologically active transition metal-based macrocycles. Material and methods. All macrocyclic compounds were synthesized by a template method and validated by molar conductiv ity, elemental studies, and spectral and magnetic studies. Antibacterial activities of all metal complexes were evaluated against Escherichia coli (MTCC 739) and Staphylococcus aureus (MTCC 731) bacterial strains by taking ampicillin as a standard reference drug. DNA photocleavage potential was explored using agarose gel electrophoresis. Results. Results revealed the formation of novel macrocyclic complexes via tetra nitrogen bond trapping of metals. Copper complexes have strong potential against S. aureus bacteria as copper and nickel both show good DNA photocleavage potential. Conclusion. The findings endorse the biomedical relevance of these macrocyclic scaffolds, suggesting avenues for further exploration in targeted drug delivery and potential clinical applications. The proposed octahedral geometry for the complexes enhances our understanding of their structural aspects. This research contributes substantively to the field, laying the foundation for future investigations in advanced antimicrobial design and application.","PeriodicalId":11828,"journal":{"name":"European Journal of Clinical and Experimental Medicine","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-03-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Clinical and Experimental Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15584/ejcem.2024.1.27","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
Introduction and aim. At present, several microbial diseases are prominent and of concern worldwide. The intent of this study was to examine the antibacterial potential of newly synthesized tetradentate macrocyclic complexes against different bacte rial strains. The macrocyclic scaffold has gained attention as a biologically active class of supramolecular chemistry due to its unique properties and ability to target various microorganisms. Thus, the goal of the present study was to develop a series of biologically active transition metal-based macrocycles. Material and methods. All macrocyclic compounds were synthesized by a template method and validated by molar conductiv ity, elemental studies, and spectral and magnetic studies. Antibacterial activities of all metal complexes were evaluated against Escherichia coli (MTCC 739) and Staphylococcus aureus (MTCC 731) bacterial strains by taking ampicillin as a standard reference drug. DNA photocleavage potential was explored using agarose gel electrophoresis. Results. Results revealed the formation of novel macrocyclic complexes via tetra nitrogen bond trapping of metals. Copper complexes have strong potential against S. aureus bacteria as copper and nickel both show good DNA photocleavage potential. Conclusion. The findings endorse the biomedical relevance of these macrocyclic scaffolds, suggesting avenues for further exploration in targeted drug delivery and potential clinical applications. The proposed octahedral geometry for the complexes enhances our understanding of their structural aspects. This research contributes substantively to the field, laying the foundation for future investigations in advanced antimicrobial design and application.
引言和目的。目前,一些微生物疾病在全球范围内十分突出,备受关注。本研究旨在考察新合成的四价大环复合物对不同菌株的抗菌潜力。大环支架因其独特的性质和针对各种微生物的能力,作为一类具有生物活性的超分子化学物质而备受关注。因此,本研究的目标是开发一系列具有生物活性的过渡金属基大环。材料和方法。所有大环化合物均采用模板法合成,并通过摩尔电导率、元素研究、光谱和磁性研究进行验证。以氨苄西林为标准参考药物,评估了所有金属复合物对大肠杆菌(MTCC 739)和金黄色葡萄球菌(MTCC 731)的抗菌活性。使用琼脂糖凝胶电泳法探讨了 DNA 的光裂解潜力。结果显示结果表明,金属通过四氮键捕获形成了新型大环配合物。铜复合物对金黄色葡萄球菌有很强的抗菌潜力,因为铜和镍都表现出良好的 DNA 光破坏潜力。结论这些研究结果证明了这些大环支架的生物医学相关性,为进一步探索靶向给药和潜在的临床应用提供了途径。为这些复合物提出的八面体几何结构增强了我们对其结构方面的理解。这项研究为该领域做出了实质性的贡献,为未来先进抗菌设计和应用的研究奠定了基础。