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Zinc(II) complexes with aromatic nitrogen-containing heterocycles as antifungal agents: Synergistic activity with clinically used drug nystatin

Authors :
Andrejević, Tina P.
Warzajtis, Beata
Glišić, Biljana
Vojnović, Sandra
Mojicević, Marija
Stevanović, Nevena Lj.
Nikodinović-Runić, Jasmina
Rychlewska, Urszula
Djuran, Milos
Andrejević, Tina P.
Warzajtis, Beata
Glišić, Biljana
Vojnović, Sandra
Mojicević, Marija
Stevanović, Nevena Lj.
Nikodinović-Runić, Jasmina
Rychlewska, Urszula
Djuran, Milos
Source :
Journal of Inorganic Biochemistry
Publication Year :
2020

Abstract

Three novel Zn(II) complexes, [ZnCl2(qz)(2)] (1), [ZnCl2(1,5-naph)](n) (2) and [ZnCl2(4,7-phen)(2)] (3), where qz is quinazoline, 1,5-naph is 1,5-naphthyridine and 4,7-phen is 4,7-phenanthroline, were synthesized by the reactions of ZnCl2 and the corresponding N-heterocyclic ligand in 1:2 molar ratio in ethanol at ambient temperature. The characterization of these complexes was done by NMR, IR and UV-Vis spectroscopy, and their crystal structures were determined by single-crystal X-ray diffraction analysis. Complexes 1 and 3 are mononuclear species, in which Zn(II) ion is tetrahedrally coordinated by two nitrogen atoms belonging to two qz or 4,7-phen ligands, respectively, and by two chloride anions, while complex 2 is a 1D coordination polymer that contains 1,5-naph as bridging ligand between two metal ions. In agar disc-diffusion assay, complexes 1-3 manifested good inhibitory activity against two investigated Candida strains (C. albicans and C. parapsilosis), while not inducing toxic effects on the healthy human fibroblast cell line (MRC-5). This activity was not fungicidal, as revealed by the broth microdilution assay, however complex 3 showed the ability to modulate Candida hyphae formation, which is an important process during infection and showed significant synergistic effect with clinically used antifungal polyene nystatin.

Details

Database :
OAIster
Journal :
Journal of Inorganic Biochemistry
Notes :
Journal of Inorganic Biochemistry
Publication Type :
Electronic Resource
Accession number :
edsoai.on1368249328
Document Type :
Electronic Resource