4.6 Article

Antifungal promising agents of zinc(II) and copper(II) derivatives based on azole drug

Journal

JOURNAL OF INORGANIC BIOCHEMISTRY
Volume 219, Issue -, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jinorgbio.2021.111401

Keywords

Metal complexes; Ketoconazole; Clotrimazole; Sporothrix brasiliensis; Candida albicans; Cryptococcus neoformans

Funding

  1. Brazilian funding agency Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)
  2. Brazilian funding agency Conselho Nacional de Desenvolvimento e Pesquisa (CNPq)
  3. Brazilian funding agency Fundacao Carlos Chagas Filho de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ)
  4. FAPESP
  5. Redoxoma project [2013/07937-8, 2016/16735-8]

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A series of metal complexes were successfully synthesized and characterized, showing promising antifungal activities. Among them, Zn-KTZ complexes exhibited broad-spectrum antifungal activity, making them potential candidates for the development of new drugs to treat mycoses.
A series of new metal complexes, [Zn(KTZ)2(Ac)2].H2O (1), [Zn(KTZ)2Cl2].0.4CH3OH (2), [Zn(KTZ)2(H2O) (NO3)](NO3) (3), [Cu(KTZ)2(Ac)2].H2O (4), [Cu(KTZ)2Cl2].3.2H2O (5), [Cu(KTZ)2(H2O)(NO3)](NO3).H2O (6), were synthesized by a reaction of ketoconazole (KTZ) with their respective zinc or copper salts under mild conditions. Similarly, six corresponding metal-CTZ (clotrimazole) complexes [Zn(CTZ)2(Ac)2].4H2O (7), [Zn (CTZ)2Cl2] (8), [Zn(CTZ)2(H2O)(NO3)](NO3).4H2O (9), [Cu(CTZ)2(Ac)2].H2O (10), [Cu(CTZ)2Cl2].2H2O (11), [Cu(CTZ)2(H2O)(NO3)](NO3).2H2O (12), were obtained. These metal complexes were characterized by elemental analyses, molar conductivity, 1H and 13C{1H} nuclear magnetic resonance, UV/Vis, and infrared spectroscopies. Further, the crystal structure for complexes 7 and 10 was determined by single-crystal X-ray diffraction. The antifungal activity of these metal complexes was evaluated against three fungal species of medical relevance: Candida albicans, Cryptococcus neoformans, and Sporothrix brasiliensis. Complexes 1 and 3 exhibited the greatest antifungal activity with a broad spectrum of action at low concentrations and high selectivity. Some morphological changes induced by these metal complexes in S. brasiliensis cells included yeasthyphae conversion, an increase in cell size and cell wall damage. The strategy of coordination of clinic drugs (KTZ and CTZ) to zinc and copper was successful, since the corresponding metal complexes were more effective than the parent drug. Particularly, the promising antifungal activities displayed by Zn-KTZ complexes make them potential candidates for the development of an alternative drug to treat mycoses.

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