Chemical and biological evaluation of moxifloxacin-benzimidazole mixed ligands complexes: Anti-cancer and anti-oxidant activities

被引:27
|
作者
Refaat, Heba M. [1 ]
El-Din, Doaa A. Noor [2 ]
机构
[1] Alexandria Univ, Chem Dept, Fac Sci, POB 426 Ibrahimia, Alexandria 21321, Egypt
[2] Medizen Pharmaceut Ind, Stabil Lab, Alexandria, Egypt
关键词
Mixed ligands; Spectra; Thermal stability; Antibacterial activity; Antioxidant; Cytotoxicity; METAL-COMPLEXES; FLUOROQUINOLONES SYNTHESIS; COPPER(II) COMPLEXES; TRANSITION SERIES; COBALT(II); PLATINUM; IONS; ANTIBACTERIAL; CYTOTOXICITY; BINDING;
D O I
10.1016/j.molstruc.2018.02.116
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Novel complexes of the formula [M(MOX)(Ben)Cl(H2O)(m)]center dot nH(2)O and [Ag(MOX)(Ben)] 3.5H(2)O; M = Co, Ni, and Zn, n = 1.5, 2 and 1, m = 0 or 2, MOX; Moxifloxacin and Ben; benzimidazole, were synthesized. Their effect on different cancer cells together with bacterial and fungal activity was determined. Formulation of the complexes was based on elemental analyses, different spectrophotometric methods (FT-IR, UV/Vis, NMR), and magnetic studies. FT-IR data indicated that the bonding of the Co(II), Ni(II) and Zn(II) ions with MOX to be achieved through the quinolone and carboxylate oxygen atoms. On the other hand Ag(I) bonded to the MOX through hydro-pyrrolopyridine nitrogen atom. TGA and DTA studies for the metal complexes showed them to possess considerable stability. Thermodynamic parameters Delta E*, Delta S* and Delta H* were evaluated and the appearance of fractional orders suggested that the reactions proceed via complicated mechanisms. The novel mixed ligands complexes were evaluated for their biological activity against the bacterial species (S. aureus) and (E. coil) and the fungal species Aspergillus flavus and Candida albicans. The complexes were found to possess better antibacterial and antifungal activities compared to the Moxifloxacin ligand. The compounds' effects were also screened for their anti-oxidant activity by DPPH method and were tested for their cytotoxicity activity against Breast cancer cell lines (MCF-7), Colon carcinoma cells (HCT) and Hepatocellular carcinoma cells (HepG2) by viability assay method. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:103 / 113
页数:11
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