Amino modified metal-organic frameworks as pH-responsive nanoplatforms for safe delivery of camptothecin

dc.contributor.affiliationInstituto Universitario Mixto de Tecnología Química
dc.contributor.authorCabrera-García, Alejandroes_ES
dc.contributor.authorCheca-Chavarria, Elisaes_ES
dc.contributor.authorRivero-Buceta, Eva María
dc.contributor.authorMORENO MANZANO, VICTORIAes_ES
dc.contributor.authorFERNANDEZ JOVER, EDUARDOes_ES
dc.contributor.authorBOTELLA ASUNCION, PABLO
dc.contributor.funderMinisterio de Economía y Competitividades_ES
dc.contributor.funderFundació Bancària Caixa d'Estalvis i Pensions de Barcelonaes_ES
dc.date.accessioned2020-11-19T04:31:51Z
dc.date.available2020-11-19T04:31:51Z
dc.date.issued2019-04-01es_ES
dc.description.abstract[EN] MIL-100(Fe) and MIL-101(Fe) metal-organic frameworks (MOFs) are excellent vehicles for drug delivery systems (DDSs) due to their high biocompatibility and stability in physiological fluids, as well as their pore diameter in the mesoporous range. Although they are appropriate for the internal diffusion of 20-(S)-camptothecin (CPT), a strongly cytotoxic molecule with excellent antitumor activity, no stable delivery system has been proposed so far for this drug based in MOFs. We here present novel DDSs based in amine functionalized MIL-100(Fe) and MIL-101(Fe) nanoMOFs with covalently bonded CPT. These CPT nanoplatforms are able to incorporate almost 20% of this molecule and show high stability at physiological pH, with no non-specific release. Based on their surface charge, some of these CPT loaded nanoMOFs present improved cell internalization in in vitro experiments. Moreover, a strong response to acid pH is observed, with up to four fold drug discharge at pH 5, which boost intracellular release by endosomolytic activity. These novel DDSs will help to achieve safe delivery of the very cytotoxic CPT, allowing to reduce the therapeutic dose and minimizing drug secondary effects. (C) 2019 Elsevier Inc. All rights reserved.en_EN
dc.description.accrualMethodSes_ES
dc.description.bibliographicCitationCabrera-García, A.; Checa-Chavarria, E.; Rivero-Buceta, EM.; Moreno Manzano, V.; Fernandez Jover, E.; Botella Asuncion, P. (2019). Amino modified metal-organic frameworks as pH-responsive nanoplatforms for safe delivery of camptothecin. Journal of Colloid and Interface Science. 541:163-174. https://doi.org/10.1016/j.jcis.2019.01.042es_ES
dc.description.sponsorshipFinancial support of the Spanish Ministry of Economy and Competitiveness (projects TEC2016-80976-R and SEV-2016-0683) is gratefully acknowledged. A.C.G. thanks the La Caixa Foundation for a Ph.D. scholarship. We fully appreciate the assistance of the Electron Microscopy Service of the Universitat Politecnica de Valencia.es_ES
dc.description.upvformatpfin174es_ES
dc.description.upvformatpinicio163es_ES
dc.description.volume541es_ES
dc.identifier.doi10.1016/j.jcis.2019.01.042es_ES
dc.identifier.issn0021-9797es_ES
dc.identifier.pmid30685611es_ES
dc.identifier.urihttps://riunet.upv.es/handle/10251/155300
dc.languageIngléses_ES
dc.publisherElsevieres_ES
dc.relation.ispartofJournal of Colloid and Interface Sciencees_ES
dc.relation.pasarelaS\406989es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//TEC2016-80976-R/ES/CONTROL DE NANOPARTICULAS MAGNETICAS PARA TERAPIA GUIADA POR IMAGEN/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//SEV-2016-0683/es_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.jcis.2019.01.042es_ES
dc.rightsReconocimiento - No comercial - Sin obra derivada (by-nc-nd)es_ES
dc.rights.accessRightsAbiertoes_ES
dc.subjectMetal-organic frameworkses_ES
dc.subjectDrug deliveryes_ES
dc.subjectPH-responsivees_ES
dc.subjectBiodegradabilityes_ES
dc.subjectCamptothecines_ES
dc.titleAmino modified metal-organic frameworks as pH-responsive nanoplatforms for safe delivery of camptothecines_ES
dc.typeArtículoes_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_ES
dspace.entity.typePublication
relation.isAuthorOfPublication30c67500-b16d-4226-946c-054a59ba6459
relation.isAuthorOfPublication1802d5fc-0898-4ed0-ab2d-31bb9105308b
relation.isAuthorOfPublication.latestForDiscovery30c67500-b16d-4226-946c-054a59ba6459
relation.isOrgUnitOfPublicationb97c2806-5147-442a-a1a8-a2c75cc2a941
relation.isOrgUnitOfPublication.latestForDiscoveryb97c2806-5147-442a-a1a8-a2c75cc2a941
upv.uuidd5862445-206f-48a2-833b-09d60baf9650es_ES

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