Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/33343
Title: Complexes of Pd(II) and Pt(II) with 9-aminoacridine: reactions with DNA and study of their antiproliferative activity
Author: Riera, X.
Moreno Martínez, Virtudes
Ciudad i Gómez, Carlos Julián
Noé Mata, Verónica
Font Bardia, Ma. Mercedes
Solans, Xavier, 1949-2007
Keywords: Medicaments antineoplàstics
Pal·ladi (Element químic)
Platí
Apoptosi
Antineoplastic agents
Palladium
Platinum
Apoptosis
Issue Date: 2007
Publisher: Hindawi
Abstract: Four new metal complexes {M = Pd(II) or Pt(II)} containing the ligand 9-aminoacridine (9AA) were prepared. The compounds were characterized by FT-IR and 1H, 13C, and 195Pt NMR spectroscopies. Crystal structure of the palladium complex of formulae [Pd(9AA)(μ-Cl)]2 · 2DMF was determined by X-ray diffraction. Two 9-acridine molecules in the imine form bind symmetrically to the metal ions in a bidentate fashion through the imine nitrogen atom and the C(1) atom of the aminoacridine closing a new five-membered ring. By reaction with phosphine or pyridine, the Cl bridges broke and compounds with general formulae [Pd(9AA)Cl(L)] (where L = PPh3 or py) were formed. A mononuclear complex of platinum of formulae [Pt(9AA)Cl(DMSO)] was also obtained by direct reaction of 9-aminoacridine and the complex [PtCl2(DMSO)2]. The capacity of the compounds to modify the secondary and tertiary structures of DNA was evaluated by means of circular dichroism and electrophoretic mobility. Both palladium and platinum compounds proved active in the modification of both the secondary and tertiary DNA structures. AFM images showed noticeable modifications of the morphology of the plasmid pBR322 DNA by the compounds probably due to the intercalation of the complexes between base pairs of the DNA molecule. Finally, the palladium complex was tested for antiproliferative activity against three different human tumor cell lines. The results suggest that the palladium complex of formula [Pd(9AA)(μ-Cl)]2 has significant antiproliferative activity, although it is less active than cisplatin.
Note: Reproducció del document publicat a: http://dx.doi.org/doi:10.1155/2007/98732
It is part of: Bioinorganic Chemistry And Applications, 2007, vol. 2007
Related resource: http://dx.doi.org/doi:10.1155/2007/98732
URI: http://hdl.handle.net/2445/33343
ISSN: 1565-3633
Appears in Collections:Articles publicats en revistes (Mineralogia, Petrologia i Geologia Aplicada)
Articles publicats en revistes (Química Inorgànica i Orgànica)
Articles publicats en revistes (Bioquímica i Biomedicina Molecular)

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