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dc.contributor.authorShaili, Evyenia
dc.contributor.authorRomero, Marίa J.
dc.contributor.authorSalassa, Luca
dc.contributor.authorWoods, Julie A.
dc.contributor.authorButler, Jennifer S.
dc.contributor.authorRomero Canelón, Isolda
dc.contributor.authorClarkson, Guy
dc.contributor.authorHabtemariam, Abraha
dc.contributor.authorSadler, Peter J.
dc.contributor.authorFarrer, Nicola J.
dc.date.accessioned2021-08-12T09:03:04Z
dc.date.available2021-08-12T09:03:04Z
dc.date.issued2021-08-14
dc.identifier.citationDalton Transactions 50(30) : 10593-10607 (2021)es_ES
dc.identifier.issn1477-9226
dc.identifier.issn1477-9234
dc.identifier.urihttp://hdl.handle.net/10810/52845
dc.description.abstractComplexes trans,trans,trans-[Pt(N-3)(2)(OH)(OCOR)(py)(2)] where py = pyridine and where OCOR = succinate (1); 4-oxo-4-propoxybutanoate (2) and N-methylisatoate (3) have been synthesized by derivation of trans, trans,trans-[Pt(OH)(2)(N-3)(2)(py)(2)] (4) and characterised by NMR and EPR spectroscopy, ESI-MS and X-ray crystallography. Irradiation of 1-3 with green (517 nm) light initiated photoreduction to Pt(II) and release of the axial ligands at a 3-fold faster rate than for 4. TD-DFT calculations showed dissociative transitions at longer wavelengths for 1 compared to 4. Complexes 1 and 2 showed greater photocytotoxicity than 4 when irradiated with 420 nm light (A2780 cell line IC50 values: 2.7 and 3.7 mu M) and complex 2 was particularly active towards the cisplatin-resistant cell line A2780cis (IC50 3.7 mu M). Unlike 4, complexes 1-3 were phototoxic under green light irradiation (517 nm), with minimal toxicity in the dark. A pK(a)(H2O) of 5.13 for the free carboxylate group was determined for 1, corresponding to an overall negative charge during biological experiments, which crucially, did not appear to impede cellular accumulation and photocytotoxicity.es_ES
dc.description.sponsorshipNF thanks the Wellcome Trust (201406/Z/16/Z); Cancer Research UK (CR-UK) grant number C5255/A18085 through the Cancer Research UK Oxford Centre and the John Fell Fund for funding. NF thanks Profs. Stephen Faulkner for support. PJS and NF thank the EPSRC (for grant EP/P030572/1 and studentship for ES), PJS also thanks the ERC (grant 247450). L. S. performed this work under the Severo Ochoa Centres of Excellence Programme run by the Spanish State Research Agency, grant no. CEX2018-000867-S (DIPC). L. S. also thanks the Spanish Multi-MetDrugs network (RED2018-102471-T) for fruitful discussiones_ES
dc.language.isoenges_ES
dc.publisherRoyal Society Of Chemistryes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/247450es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectanticancer complexeses_ES
dc.subjectglutathione levelses_ES
dc.subjectphotochemistryes_ES
dc.subjectcarboxylationes_ES
dc.subjectcytotoxicityes_ES
dc.subjectreductiones_ES
dc.subjectligandses_ES
dc.subjectserieses_ES
dc.subjectcopperes_ES
dc.subjectbloodes_ES
dc.titlePlatinum(IV)-azido monocarboxylato complexes are photocytotoxic under irradiation with visible lightes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY)es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://pubs-rsc-org.ehu.idm.oclc.org/en/content/articlelanding/2021/DT/D1DT01730Fes_ES
dc.identifier.doi10.1039/d1dt01730f
dc.contributor.funderEuropean Commission
dc.departamentoesPolímeros y Materiales Avanzados: Física, Química y Tecnologíaes_ES
dc.departamentoeuPolimero eta Material Aurreratuak: Fisika, Kimika eta Teknologiaes_ES


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This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY)
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