Dendrimers as Innovative Radiopharmaceuticals in Cancer Radionanotherapy

dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Molecularesgl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánicagl
dc.contributor.authorLiko, Flonja
dc.contributor.authorHindré, François
dc.contributor.authorFernández Megía, Eduardo
dc.date.accessioned2018-07-04T12:20:52Z
dc.date.available2018-07-04T12:20:52Z
dc.date.issued2016
dc.description.abstractRadiotherapy is one of the most commonly used cancer treatments, with an estimate of 40% success that could be improved further if more efficient targeting and retention of radiation at the tumor site were achieved. This review focuses on the use of dendrimers in radionanotherapy, an emerging technology aimed to improve the efficiency of radiotherapy by implementing nanovectorization, an already established praxis in drug delivery and diagnosis. The labeling of dendrimers with radionuclides also aims to reduce the dose of radiolabeled materials and, hence, their toxicity and tumor resistance. Examples of radiolabeled dendrimers with alpha, beta, and Auger electron emitters are commented, along with the use of dendrimers in boron neutron capture therapy (BNCT). The conjugation of radiolabeled dendrimers to monoclonal antibodies for a more efficient targeting and the application of dendrimers in gene delivery radiotherapy are also coveredgl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThis work was financially supported by the Spanish Government (CTQ2015-69021-R, CTQ2012-34790) and the Xunta de Galicia (GRC2014/040) and by the “Institut National de la Santé et de la Recherche Médicale” (INSERM), by the “Axe Vectorisation and Radiothérapies” and the “Réseau Gliome Grand Ouest” (ReGGO) of the“Cancéropôle Grand-Ouest”. The coauthors of this manuscript are also members of the LabEx IRON “Innovative Radiopharmaceuticals in Oncologyand Neurology” as part of the french government program “Investissements d’Avenir”. F.L. thanks the European Commission, Education, Audiovisual and Cultural Executive Agency (EACEA) for an Erasmus Mundus Grant under the NanoFar Joint Doctoral Programgl
dc.identifier.citationLiko, F., Hindré, F., & Fernandez-Megia, E. (2016). Dendrimers as Innovative Radiopharmaceuticals in Cancer Radionanotherapy. Biomacromolecules, 17(10), 3103-3114. doi: 10.1021/acs.biomac.6b00929gl
dc.identifier.doi10.1021/acs.biomac.6b00929
dc.identifier.essn1526-4602
dc.identifier.issn1525-7797
dc.identifier.urihttp://hdl.handle.net/10347/16953
dc.language.isoenggl
dc.publisherAmerican Chemical Societygl
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2015-69021-R/ES/MICELAS DENDRITICAS EN TERAPIA Y DIAGNOSTICO: CONTROL DE LA ARQUITECTURA Y ACTIVIDAD A PARTIR DE LA ESTRUCTURA MOLECULAR
dc.relation.publisherversionhttps://doi.org/10.1021/acs.biomac.6b00929gl
dc.rights© 2016 American Chemical Societygl
dc.rights.accessRightsopen accessgl
dc.subjectDendrimersgl
dc.subjectRadiomedicinegl
dc.subjectRadiotherapygl
dc.subjectCancergl
dc.subjectRadioimmunotherapygl
dc.titleDendrimers as Innovative Radiopharmaceuticals in Cancer Radionanotherapygl
dc.typejournal articlegl
dc.type.hasVersionAMgl
dspace.entity.typePublication
relation.isAuthorOfPublicationfe5ace22-ce25-4507-aacf-a74fa1010319
relation.isAuthorOfPublication.latestForDiscoveryfe5ace22-ce25-4507-aacf-a74fa1010319

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