Complexes of Pd(II) and Pt(II) with 9-aminoacridine: reactions with DNA and study of their antiproliferative activity

dc.contributor.authorRiera, X.
dc.contributor.authorMoreno Martínez, Virtudes
dc.contributor.authorCiudad i Gómez, Carlos Julián
dc.contributor.authorNoé Mata, Verónica
dc.contributor.authorFont Bardia, Ma. Mercedes
dc.contributor.authorSolans, Xavier, 1949-2007
dc.date.accessioned2013-01-14T10:01:37Z
dc.date.available2013-01-14T10:01:37Z
dc.date.issued2007
dc.date.updated2013-01-14T10:01:37Z
dc.description.abstractFour 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.
dc.format.extent15 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec555443
dc.identifier.issn1565-3633
dc.identifier.pmid18364995
dc.identifier.urihttps://hdl.handle.net/2445/33343
dc.language.isoeng
dc.publisherHindawi
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/doi:10.1155/2007/98732
dc.relation.ispartofBioinorganic Chemistry And Applications, 2007, vol. 2007
dc.relation.urihttp://dx.doi.org/doi:10.1155/2007/98732
dc.rightscc-by (c) Riera, X. et al., 2007
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Bioquímica i Biomedicina Molecular)
dc.subject.classificationMedicaments antineoplàstics
dc.subject.classificationPal·ladi (Element químic)
dc.subject.classificationPlatí
dc.subject.classificationApoptosi
dc.subject.otherAntineoplastic agents
dc.subject.otherPalladium
dc.subject.otherPlatinum
dc.subject.otherApoptosis
dc.titleComplexes of Pd(II) and Pt(II) with 9-aminoacridine: reactions with DNA and study of their antiproliferative activityeng
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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