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Cytotoxic effect, generation of reactive oxygen/nitrogen species and electrochemical properties of Cu(ii) complexes in comparison to half-sandwich complexes of Ru(ii) with aminochromone derivatives

This paper describes the synthesis of new 6-aminoflavone (6AFl (3)) and 6-aminochromone (6AC (4)) complexes with Cu(ii) and Ru(ii) ions ([Cu(6AC)(2)Cl(2)] (3a), [Cu(6AFl)(2)Cl(2)] (4a), [Ru(p-cymene)(6AC)Cl(2)] (4b)) and comparison of their properties with the previously described 7-aminoflavone (7A...

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Autores principales: Mucha, Paulina, Hikisz, Pawel, Gwoździński, Krzysztof, Krajewska, Urszula, Leniart, Andrzej, Budzisz, Elzbieta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072735/
https://www.ncbi.nlm.nih.gov/pubmed/35530753
http://dx.doi.org/10.1039/c9ra05971g
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author Mucha, Paulina
Hikisz, Pawel
Gwoździński, Krzysztof
Krajewska, Urszula
Leniart, Andrzej
Budzisz, Elzbieta
author_facet Mucha, Paulina
Hikisz, Pawel
Gwoździński, Krzysztof
Krajewska, Urszula
Leniart, Andrzej
Budzisz, Elzbieta
author_sort Mucha, Paulina
collection PubMed
description This paper describes the synthesis of new 6-aminoflavone (6AFl (3)) and 6-aminochromone (6AC (4)) complexes with Cu(ii) and Ru(ii) ions ([Cu(6AC)(2)Cl(2)] (3a), [Cu(6AFl)(2)Cl(2)] (4a), [Ru(p-cymene)(6AC)Cl(2)] (4b)) and comparison of their properties with the previously described 7-aminoflavone (7AFl (1)) and 7-amino-2-methylchromone (7A2MC (2)) analogues. The cytotoxic effect of all these complexes against two human leukaemia cell lines (HL-60 and NALM-6), melanoma WM-115 cells and COLO205 cells, is determined. The cytotoxicity of copper(ii) complexes, especially [Cu(6AFl)(2)Cl(2)] (3a) was higher than ruthenium(ii) complexes with the same ligands. Their cytotoxic potency was also stronger in comparison to the referential agents like cisplatin. The pro-oxidative properties were determined for the most active complexes and their ability to generate ROS (reactive oxygen species)/RNS (reactive nitrogen species) in cancer cells was confirmed. The type of ligand and the chemical structure of the tested complexes had an influence on the level of ROS/RNS generated in cancer cells. The redox properties of the copper complex compounds were evaluated by cyclic voltammetry, and compared with the data for Ru(ii) complexes. The reduction and oxidation processes of Ru(iii)/Ru(ii) and Cu(ii)/Cu(i) were described as quasi-reversible.
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spelling pubmed-90727352022-05-06 Cytotoxic effect, generation of reactive oxygen/nitrogen species and electrochemical properties of Cu(ii) complexes in comparison to half-sandwich complexes of Ru(ii) with aminochromone derivatives Mucha, Paulina Hikisz, Pawel Gwoździński, Krzysztof Krajewska, Urszula Leniart, Andrzej Budzisz, Elzbieta RSC Adv Chemistry This paper describes the synthesis of new 6-aminoflavone (6AFl (3)) and 6-aminochromone (6AC (4)) complexes with Cu(ii) and Ru(ii) ions ([Cu(6AC)(2)Cl(2)] (3a), [Cu(6AFl)(2)Cl(2)] (4a), [Ru(p-cymene)(6AC)Cl(2)] (4b)) and comparison of their properties with the previously described 7-aminoflavone (7AFl (1)) and 7-amino-2-methylchromone (7A2MC (2)) analogues. The cytotoxic effect of all these complexes against two human leukaemia cell lines (HL-60 and NALM-6), melanoma WM-115 cells and COLO205 cells, is determined. The cytotoxicity of copper(ii) complexes, especially [Cu(6AFl)(2)Cl(2)] (3a) was higher than ruthenium(ii) complexes with the same ligands. Their cytotoxic potency was also stronger in comparison to the referential agents like cisplatin. The pro-oxidative properties were determined for the most active complexes and their ability to generate ROS (reactive oxygen species)/RNS (reactive nitrogen species) in cancer cells was confirmed. The type of ligand and the chemical structure of the tested complexes had an influence on the level of ROS/RNS generated in cancer cells. The redox properties of the copper complex compounds were evaluated by cyclic voltammetry, and compared with the data for Ru(ii) complexes. The reduction and oxidation processes of Ru(iii)/Ru(ii) and Cu(ii)/Cu(i) were described as quasi-reversible. The Royal Society of Chemistry 2019-10-08 /pmc/articles/PMC9072735/ /pubmed/35530753 http://dx.doi.org/10.1039/c9ra05971g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Mucha, Paulina
Hikisz, Pawel
Gwoździński, Krzysztof
Krajewska, Urszula
Leniart, Andrzej
Budzisz, Elzbieta
Cytotoxic effect, generation of reactive oxygen/nitrogen species and electrochemical properties of Cu(ii) complexes in comparison to half-sandwich complexes of Ru(ii) with aminochromone derivatives
title Cytotoxic effect, generation of reactive oxygen/nitrogen species and electrochemical properties of Cu(ii) complexes in comparison to half-sandwich complexes of Ru(ii) with aminochromone derivatives
title_full Cytotoxic effect, generation of reactive oxygen/nitrogen species and electrochemical properties of Cu(ii) complexes in comparison to half-sandwich complexes of Ru(ii) with aminochromone derivatives
title_fullStr Cytotoxic effect, generation of reactive oxygen/nitrogen species and electrochemical properties of Cu(ii) complexes in comparison to half-sandwich complexes of Ru(ii) with aminochromone derivatives
title_full_unstemmed Cytotoxic effect, generation of reactive oxygen/nitrogen species and electrochemical properties of Cu(ii) complexes in comparison to half-sandwich complexes of Ru(ii) with aminochromone derivatives
title_short Cytotoxic effect, generation of reactive oxygen/nitrogen species and electrochemical properties of Cu(ii) complexes in comparison to half-sandwich complexes of Ru(ii) with aminochromone derivatives
title_sort cytotoxic effect, generation of reactive oxygen/nitrogen species and electrochemical properties of cu(ii) complexes in comparison to half-sandwich complexes of ru(ii) with aminochromone derivatives
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072735/
https://www.ncbi.nlm.nih.gov/pubmed/35530753
http://dx.doi.org/10.1039/c9ra05971g
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