Department of Chemistry and Biochemistry, Faculty of AgriSciences, Mendel University in Brno, CZ-613 00 Brno, Czech Republic.
Central European Institute of Technology, Brno University of Technology, CZ-61200 Brno, Czech Republic.
Int J Mol Sci. 2020 Apr 10;21(7):2656. doi: 10.3390/ijms21072656.
The current epidemic of antibiotic-resistant infections urges to develop alternatives to less-effective antibiotics. To assess anti-bacterial potential, a novel coordinate compound (RU-S4) was synthesized using ruthenium-Schiff base-benzimidazole ligand, where ruthenium chloride was used as the central atom. RU-S4 was characterized by scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDS), and Raman spectroscopy. Antibacterial effect of RU-S4 was studied against (NCTC 8511), vancomycin-resistant (VRSA) (CCM 1767), methicillin-resistant (MRSA) (ST239: SCCmecIIIA), and hospital isolate . The antibacterial activity of RU-S4 was checked by growth curve analysis and the outcome was supported by optical microscopy imaging and fluorescence LIVE/DEAD cell imaging. In vivo (balb/c mice) infection model prepared with VRSA (CCM 1767) and treated with RU-S4. In our experimental conditions, all infected mice were cured. The interaction of coordination compound with bacterial cells were further confirmed by cryo-scanning electron microscope (Cryo-SEM). RU-S4 was completely non-toxic against mammalian cells and in mice and subsequently treated with synthesized RU-S4.
当前抗生素耐药性感染的流行促使人们开发替代效果较差的抗生素的方法。为了评估抗菌潜力,使用钌-Schiff 碱-苯并咪唑配体合成了一种新型配位化合物(RU-S4),其中使用氯化钌作为中心原子。通过扫描电子显微镜(SEM)、能谱(EDS)和拉曼光谱对 RU-S4 进行了表征。RU-S4 对 (NCTC 8511)、万古霉素耐药 (VRSA)(CCM 1767)、耐甲氧西林 (MRSA)(ST239:SCCmecIIIA)和医院分离株 进行了抗菌作用研究。通过生长曲线分析检查 RU-S4 的抗菌活性,并用光学显微镜成像和荧光 LIVE/DEAD 细胞成像支持结果。用 VRSA(CCM 1767)制备体内(balb/c 小鼠)感染模型,并用 RU-S4 治疗。在我们的实验条件下,所有感染的小鼠都被治愈了。通过冷冻扫描电子显微镜(Cryo-SEM)进一步证实了配位化合物与细菌细胞的相互作用。RU-S4 对哺乳动物细胞完全没有毒性,并且在小鼠中没有毒性,随后用合成的 RU-S4 进行了处理。