[:pb]Authors: De Oliveira, L. P.; Carneiro, Z. A.; Ribeiro, C. M.; Lima, M. F.; Paixão, D. A.; Pivatto, M.; De Souza, M. V.N.; Teixeira, L. R.; Lopes, C. D. ; De Albuquerque, S.; Pavan, F. R. ; Guerra, W.
Source: Journal of Inorganic Biochemistry, v. 183, p. 77-83, 2018
Publisher: Science Direct
Abstract
This work describes the synthesis, characterization and biological evaluation of three platinum complexes of the type [Pt(DMSO)(L)Cl]Cl, in which L represents a fluoroquinolone, namely, ciprofloxacin (cpl), ofloxacin (ofl), or sparfloxacin (spf). The new complexes were characterized by elemental analysis, high-resolution mass spectrometry (HRESIMS) and 1H, 13C and 195Pt NMR (nuclear magnetic resonance). The spectral data suggest that the fluoroquinolones act as bidentate ligands coordinated to Pt(II) through the nitrogen atoms of the piperazine ring. Microbiological assays against wild type Mycobacterium tuberculosis (ATCC 27294) showed that all complexes have been very potent, exhibiting antitubercular potency at concentrations <2 μM, although none of the complexes presented higher potency than established anti-TB drugs. As to the resistant strains, the complex with sparfloxacin, [Pt(DMSO)(spf)Cl]Cl exhibited the best potential against most Mycobacterium tuberculosis clinical isolates. The cytotoxicity of these compounds was also evaluated in three breast cell lines: MCF-10 (a healthy cell), MCF-7 (a hormone responsive cancer cell) and MDA-MB-231 (triple negative breast cancer cell). In both tumor cell lines, [Pt(DMSO)(spf)Cl]Cl was more active and more selective than cisplatin. Flow cytometry analysis revealed that [Pt(DMSO)(spf)Cl]Cl induced late apoptotic cell death in MDA-MB-231 cells.
Keywords: platinum complexes, fluoroquinolone, mycobacterium tuberculosis, resistant strains, cytotoxicity, apoptosis
Document Type: Research Article
DOI: 10.1016/j.jinorgbio.2018.03.010
Publication date: Junho de 2018[:]
