Synthesis, Characterization, and Cytotoxic Activity of New Lanthanum(III) Complexes of Bis‐Coumarins
Author(s) -
Irena Kostova,
Georgi Momekov,
Tzvetomira Tzanova,
Margarita Karaivanova
Publication year - 2006
Publication title -
bioinorganic chemistry and applications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.865
H-Index - 35
eISSN - 1565-3633
pISSN - 1687-479X
DOI - 10.1155/bca/2006/25651
Subject(s) - chemistry , lanthanum , cytotoxic t cell , combinatorial chemistry , characterization (materials science) , cytotoxicity , coumarin , stereochemistry , nanotechnology , organic chemistry , biochemistry , in vitro , materials science
Complexes of lanthanum(III) with bis-coumarins: 3,3′-benzylidene-bis(4-hydroxy-2H-1-benzopyran-2-one) ( H 2 L1) and bis(4-hydroxy-2-oxo-2H-chromen-3-yl)-(1H-pyrazol-3-yl)-methane ( H 2 L2) were synthesized by reaction of lanthanum(III) salt and the ligands, in amounts equal to metal : ligand molar ratio of 1 : 2. The complexes were prepared by adding an aqueous solution of lanthanum(III) salt to an aqueous solution of the ligand subsequently raising the pH of the mixture gradually to circa 5.0 by adding dilute solution of sodium hydroxide. The lanthanum(III) complexes with bis-coumarins were characterized by different physicochemical methods—elemental analysis, IR-, 1 H -, and 13 C -NMR-spectroscopies, and mass spectral data. The spectral data of lanthanum(III) complexes were interpreted on the basis of comparison with the spectra of the free ligands. This analysis showed that in the La(III) complexes, the ligands coordinated to the metal ion through both deprotonated hydroxyl groups. On the basis of the ν (C=O) red shift observed, participation of the carbonyl groups in the coordination with the metal ion was also suggested. In the present study, we performed a cytotoxic-effects screening of the lanthanum complexes with H 2 L1 and H 2 L2 in a panel of human tumor cell lines, using the standard MTT-dye reduction assay for cell viability. The panel consisted of the acute myeloid leukemia-derived HL-60 and the chronic myeloid leukemia-derived BV-173. Following a 24- hour treatment of BV-173 cells with lanthanum complex of H 2 L1 at 100 or 200 μ M led to a DNA-laddering. The findings suggest that the observed cytotoxicity of the lanthanum complex of H 2 L1 on BV-173 is at least partly mediated through induction of programmed cell death.
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