SYNTHESIS OF RUTHENIUM COMPLEXES AND ASSESSING THEIR ANTICANCER AND ANTIBACTERIAL EFFECTS

被引:0
|
作者
Zeiz, Ali [1 ]
Chayya, Suzanne [2 ]
Kassem, Zeinab [3 ]
Hijazi, Akram [3 ]
Khawaja, Ghada [1 ]
El-Dakdouki, Mohammad H. [2 ]
机构
[1] Beirut Arab Univ, Fac Sci, Dept Biol Sci, POB 11-5020, Beirut 11072809, Lebanon
[2] Beirut Arab Univ, Dept Chem, Fac Sci, POB 11-5020, Beirut 11072809, Lebanon
[3] Lebanese Univ, Doctoral Sch Sci & Technol, Platform Res & Anal Environm Sci PRASE, Beirut, Lebanon
关键词
Ru(dppz)(DMSO)(2)Cl-2; molecular docking; Western blot; antibacterial effect; CELLULAR UPTAKE; DNA-BINDING; POLYPYRIDYL COMPLEXES; MOLECULAR DOCKING; LIGHT SWITCH; APOPTOSIS; CANCER; DRUGS; PHOTOCLEAVAGE; CYTOTOXICITY;
D O I
10.31925/farmacia.2023.6.3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ruthenium (Ru) complexes exhibit intriguing biological effects, including potent antibacterial and anticancer activities. The aim of this study was to prepare Ru(dppz)(DMSO)(2)Cl-2 complex from cis-fac-dichlorotetrakis(dimethylsulfoxide)ruthenium(II) precursor (cis-Ru(DMSO)(4)Cl-2), and assess its anticancer and antibacterial activities. The complex was characterized by NMR and FTIR spectroscopies. The physiochemical properties of the prepared complexes were predicted by employing MolSoft software and its DNA binding potential was assessed using molecular docking. The complex displayed an intercalative mode of DNA binding with a binding affinity of-15.93 kcal/mol and a hydrogen bonding of 2.5 angstrom. Additionally, Ru complex exhibited a promising antibacterial effect against E. coli, E. faecalis, P. aeruginosa and S. aureus at a minimum inhibitory concentration (MIC) of similar to 30 mu g/mL. The cytotoxic activity of cis-Ru(DMSO)(4)Cl-2 and Ru(dppz)(DMSO)(2)Cl-2 complexes against colorectal (HCT-116) and breast cancer (MCF-7) cell lines was elucidated by using the MTT cell viability assay, and the latter complex displayed an intriguing low IC50 value (12.6 mu M) in HCT-116 cells. The precise molecular mechanism of action of Ru(dppz)(DMSO)(2)Cl-2 complex was deciphered by tracking the expression levels of key apoptotic proteins, namely p53, Bax and Bcl-2. Western blotting analysis showed that the anticancer activity is mediated by the complex's ability to activate the mitochondrial apoptotic pathway, as evident by modulating the expression level of p53, Bax and Bcl-2 proteins.
引用
收藏
页码:1129 / 1142
页数:14
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