Publicação:
Multi-spectroscopic monitoring of cisplatin-derived species delivery from ureasil polyether hybrid matrix

dc.contributor.authorMolina, Eduardo Ferreira [UNESP]
dc.contributor.authorSantilli, Celso Valentim [UNESP]
dc.contributor.authorPulcinelli, Sandra Helena [UNESP]
dc.contributor.authorBlanchandin, Stephanie
dc.contributor.authorBaudelet, Francois
dc.contributor.authorBriois, Valerie
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionSynchrotron SOLEIL
dc.date.accessioned2014-05-20T14:18:18Z
dc.date.available2014-05-20T14:18:18Z
dc.date.issued2011-01-01
dc.description.abstractDriven by the challenges involved in the development of new advanced materials with unusual drug delivery profiles capable of improving the therapeutic and toxicological properties of existing cancer chemotherapy, the one-pot sol-gel synthesis of flexible, transparent and insoluble urea-cross-linked polyether-siloxane hybrids has been recently developed. In this one-pot synthesis, the strong interaction between the antitumor cisplatin (CisPt) molecules and the ureasil-poly(propylene oxide) (PPO) hybrid matrix gives rise to the incorporation and release of an unknown CisPt-derived species, hindering the quantitative determination of the drug release pattern from the conventional UV-Vis absorption technique. In this article, we report the use of an original synchrotron radiation calibration method based on the combination of XAS and UV-Vis for the quantitative determination of the amount of Pt-based molecules released in water. Thanks to the combination of UV-Vis, XAS and Raman techniques, we demonstrated that both the CisPt molecules and the CisPt-derived species are loaded into an ureasil-PPO/ureasil-poly(ethylene oxide) (PEO) hybrid blend matrix. The experimentally determined molar extinction coefficient of the CisPt-derived species loaded into ureasil-PPO hybrid matrix enabled the simultaneous time-resolved monitoring of each Pt species released from this hybrid blend matrix.en
dc.description.affiliationInst Quim UNESP, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationSynchrotron SOLEIL, F-91192 Gif Sur Yvette, France
dc.description.affiliationUnespInst Quim UNESP, BR-14800900 Araraquara, SP, Brazil
dc.format.extent687-699
dc.identifierhttp://dx.doi.org/10.1080/01411594.2010.548754
dc.identifier.citationPhase Transitions. Abingdon: Taylor & Francis Ltd, v. 84, n. 8, p. 687-699, 2011.
dc.identifier.doi10.1080/01411594.2010.548754
dc.identifier.issn0141-1594
dc.identifier.lattes5584298681870865
dc.identifier.lattes9971202585286967
dc.identifier.orcid0000-0002-8356-8093
dc.identifier.urihttp://hdl.handle.net/11449/25508
dc.identifier.wosWOS:000299703700003
dc.language.isoeng
dc.publisherTaylor & Francis Ltd
dc.relation.ispartofPhase Transitions
dc.relation.ispartofjcr1.028
dc.relation.ispartofsjr0,233
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjecttime resolved X-ray absorptionen
dc.subjectRaman scatteringen
dc.subjectUV-Visible absorptionen
dc.subjectdrug deliveryen
dc.titleMulti-spectroscopic monitoring of cisplatin-derived species delivery from ureasil polyether hybrid matrixen
dc.typeArtigo
dcterms.licensehttp://journalauthors.tandf.co.uk/permissions/reusingOwnWork.asp
dcterms.rightsHolderTaylor & Francis Ltd
dspace.entity.typePublication
unesp.author.lattes9971202585286967
unesp.author.lattes5584298681870865[2]
unesp.author.orcid0000-0002-8356-8093[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentFísico-Química - IQARpt

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