The Antimicrobial Efficacy of Copper Complexes: A Review.

IF 4.3 2区 医学 Q1 INFECTIOUS DISEASES
Kwanele Ngece, Vuyolwethu Khwaza, Athandwa M Paca, Blessing A Aderibigbe
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引用次数: 0

Abstract

The alarming increase in antimicrobial resistance has intensified the search for novel therapeutic agents capable of combating resistant microbial strains. Copper complexes have emerged as promising antimicrobial agents due to their intrinsic redox activity, ability to disrupt microbial membranes, and interactions with vital biomolecules such as DNA and proteins. This review critically evaluates the antimicrobial potential of copper complexes reported between 2018 and 2025, emphasizing their structural diversity, mechanisms of action, and biological performance against a wide range of bacterial and fungal pathogens. Key findings reveal that Schiff base copper complexes, amino acid derivatives, heterocyclic ligands, and mixed-ligand systems exhibit potent antimicrobial activities, often surpassing standard antibiotics. Mechanistically, copper complexes induce reactive oxygen species (ROS) generation, inhibit enzyme function, cause DNA cleavage, and compromise cell membrane integrity. Furthermore, structure-activity relationship (SAR) analyses indicate that ligand type, coordination geometry, and lipophilicity significantly influence antimicrobial efficacy. Overall, the reviewed studies support the development of copper-based compounds as viable candidates for antimicrobial drug development. This review also identifies current challenges and gaps in knowledge, such as limited in vivo studies and toxicity assessments, which must be addressed to advance these compounds toward clinical application.

铜配合物的抗菌效果研究进展。
抗菌素耐药性的惊人增长加强了对能够对抗耐药微生物菌株的新型治疗剂的研究。铜配合物由于其内在的氧化还原活性、破坏微生物膜的能力以及与重要生物分子(如DNA和蛋白质)的相互作用而成为有前途的抗菌剂。本文对2018年至2025年间报道的铜配合物的抗菌潜力进行了批判性评估,强调了它们的结构多样性、作用机制以及对多种细菌和真菌病原体的生物学性能。主要研究结果表明,希夫碱铜配合物、氨基酸衍生物、杂环配体和混合配体系统具有强大的抗菌活性,通常超过标准抗生素。从机制上讲,铜配合物诱导活性氧(ROS)的产生,抑制酶的功能,导致DNA分裂,并损害细胞膜的完整性。此外,构效关系(SAR)分析表明,配体类型、配位几何形状和亲脂性显著影响抗菌效果。总的来说,综述的研究支持开发铜基化合物作为抗菌药物开发的可行候选者。本综述还指出了当前的挑战和知识空白,例如有限的体内研究和毒性评估,必须解决这些问题,以推进这些化合物的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Antibiotics-Basel
Antibiotics-Basel Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
7.30
自引率
14.60%
发文量
1547
审稿时长
11 weeks
期刊介绍: Antibiotics (ISSN 2079-6382) is an open access, peer reviewed journal on all aspects of antibiotics. Antibiotics is a multi-disciplinary journal encompassing the general fields of biochemistry, chemistry, genetics, microbiology and pharmacology. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of papers.
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