Similarities and differences in d6 low-spin ruthenium, rhodium and iridium half-sandwich complexes: synthesis, structure, cytotoxicity and interaction with biological targets - Publication - Bridge of Knowledge

Your account

login

Search

Similarities and differences in d6 low-spin ruthenium, rhodium and iridium half-sandwich complexes: synthesis, structure, cytotoxicity and interaction with biological targets

Abstract

In this paper, we discussed the similarities and diferences in d6 low-spin half-sandwich ruthenium, rhodium and iridium complexes containing 2,2′-biimidazole (H2biim). Three new complexes, {[RuCl(H2biim)(η6 -p-cymene)]PF6}2·H2O (1), [(η5 - Cp)RhCl(H2biim)]PF6 (2), and [(η5 -Cp)IrCl(H2biim)]PF6 (3), were fully characterized by CHN, X-ray difraction analysis, UV–Vis, FTIR, and 1 H, 13C and 15N NMR spectroscopies. The complexes exhibit a typical pseudooctahedral piano-stool geometry, in which the aromatic arene ring (p-cymene or Cp) forms the seat, while the bidentate 2,2′-biimidazole and chloride ion form the three legs of the piano stool. Moreover, the cytotoxic activities of the compounds were examined in the LoVo, HL-60, MV-4-11, MCF-7 human cancer cell lines and BALB/3T3 normal mouse fbroblasts. Notably, the investigated complexes showed no cytotoxic efects towards the normal BALB/3T3 cell line compared to cisplatin, which has an IC50 value of 2.20 µg. Importantly, 1 displayed the highest activity against HL-60 (IC50 4.35 µg). To predict a binding mode, we explored the potential interactions of the metal complexes with CT-DNA and protein using UV absorption and circular dichroism. The obtained data suggest that the complexes could interact with CT-DNA via an outside binding mode. Moreover, binding of the complexes with the GSH via UV–Vis and ESI mass spectra was determined. Comparative studies have shown that the rhodium complex (2) is the most GSH reactive, which is probably responsible for its deactivation towards LoVo and MCF-7 tumour cells. The infuence of the metal ion on the biological activity of isostructural Rh(III) and Ir(III) complexes was an important goal of the presented investigation.

Citations

  • 2 9

    CrossRef

  • 0

    Web of Science

  • 2 9

    Scopus

Authors (7)

Cite as

Full text

download paper
downloaded 53 times
Publication version
Accepted or Published Version
DOI:
Digital Object Identifier (open in new tab) 10.1007/s00775-019-01665-2
License
Creative Commons: CC-BY open in new tab

Keywords

Details

Category:
Articles
Type:
artykuły w czasopismach
Published in:
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY no. 24, pages 591 - 606,
ISSN: 0949-8257
Language:
English
Publication year:
2019
Bibliographic description:
Gilewska A., Barszcz B., Masternak J., Kazimierczuk K., Sitkowski J., Wietrzyk J., Turlej E.: Similarities and differences in d6 low-spin ruthenium, rhodium and iridium half-sandwich complexes: synthesis, structure, cytotoxicity and interaction with biological targets// JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY -Vol. 24,iss. 4 (2019), s.591-606
DOI:
Digital Object Identifier (open in new tab) 10.1007/s00775-019-01665-2
Verified by:
Gdańsk University of Technology

seen 147 times

Recommended for you

Synthesis, physicochemical and theoretical studies on new rhodium and ruthenium dimers. Relationship between structure and cytotoxic activity

2018

Synthesis, structure, DNA binding and anticancer activity of mixed ligand ruthenium(II) complex

2018

Synthesis, crystal structure and cytotoxic activity of ruthenium(II) piano-stool complex with N,N-chelating ligand

2016

Ruthenium(II) and Iridium(III) Complexes as Tested Materials for New Anticancer Agents

  • J. Masternak,
  • A. Gilewska,
  • B. Barszcz
  • + 6 authors
2020
Meta Tags