钴(II)单独与1,10-菲罗啉及与胞苷混合的配合物:合成及抗菌活性

Abebe Atakilt, Girma Bayissa, Abreham Sendek, M. Kibret
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引用次数: 3

摘要

钴可以与一系列生物分子结合形成复合物,适用于各种生物应用。不同的配体可以用来调整钴化合物的性质,使其配体交换率接近于细胞过程的配体交换率。本研究以1,10-菲罗啉单独合成[Co(phen) 2 (h2o) 2]Cl 2,以1,10-菲罗啉和胞苷合成[Co(phen) 2 (Cyt) h2o]Cl。通过卤化物测试、电导测试以及光谱分析(原子吸收光谱、红外光谱、紫外可见光谱)对合成进行了验证。测定了两种金属配合物对金黄色葡萄球菌、耐甲氧西林金黄色葡萄球菌(MRSA)、肺炎链球菌、大肠杆菌、肺炎克雷伯菌和博氏谢氏菌的体外抑菌活性。这些配合物对某些细菌的活性优于市售对照药物(氯霉素和环丙沙星)。[Co(phen) 2 (Cyt)(h2o)]Cl对MRSA(4.8%)和大肠杆菌(21.4%)的抑制作用优于氯霉素。同样,对MRSA和大肠杆菌的抑制区分别比环丙沙星多11.9%和22.8%。另一方面,[Co(Phen) 2 (h2o) 2]Cl对金黄色葡萄球菌和波氏葡萄球菌的抑制区分别增加5.3%和3.0%,优于环丙沙星。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cobalt(II) complexes with 1,10-phenanthroline alone and mixed with cytoside: Synthesis and antibacterial activities
Cobalt can bind to a range of biomolecules forming complexes that are suitable for use in various biological applications. Different ligands could be used to tune the properties of cobalt compounds whose ligand exchange rates become close to those of cellular processes.  In this study, two complexes were synthesized from 1,10-phenanthroline alone as [Co(phen) 2 (H 2 O) 2 ]Cl 2 and from both 1,10-phenanthroline and cytoside as [Co(phen) 2 (Cyt)H 2 O]Cl. The synthesis was checked using halide test, conductance measurement as well as spectroscopic (AAS, FTIR, Uv-vis) analysis. In vitro antibacterial activities of the two metal complexes were tested against Staphylococcus aureu s, methicilin resistant staphylococcus aureus (MRSA), Streptococcus pneumoniae, Escherichia coli , Klebsiella pneumoniae and Shegella boydii. These complexes showed better activities than the commercially available control drugs (chloramphenicol and ciprofloxacin) against certain strains of bacteria. Better inhibition zones were exhibited by [Co(phen) 2 (Cyt)(H 2 O)]Cl on MRSA (4.8%) and E. coli (21.4%) than chloramphenicol. Likewise, 11.9% and 22.8% more zones of inhibition than ciprofloxacin were shown against MRSA and E. coli , respectively. On the other hand, [Co(Phen) 2 (H 2 O) 2 ]Cl showed 5.3% and 3.0% more zones of inhibition against S. aurous and S. boydii ,  respectively, better than ciprofloxacin.
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