Publication:
Micellar Iron Oxide Nanoparticles Coated with Anti-Tumor Glycosides

dc.contributor.authorGroult, Hugo
dc.contributor.authorGarcia-Alvarez, Isabel
dc.contributor.authorRomero-Ramirez, Lorenzo
dc.contributor.authorNieto-Sampedro, Manuel
dc.contributor.authorHerranz, Fernando
dc.contributor.authorFernandez-Mayoralas, Alfonso
dc.contributor.authorRuiz-Cabello, Jesus
dc.contributor.funderUnión Europea. Comisión Europea
dc.contributor.funderMinisterio de Economía y Competitividad (España)
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderComunidad de Madrid (España)
dc.date.accessioned2018-10-26T07:59:27Z
dc.date.available2018-10-26T07:59:27Z
dc.date.issued2018
dc.description.abstractThe synthesis procedure of nanoparticles based on thermal degradation produces organic solvent dispersible iron oxide nanoparticles (OA-IONP) with oleic acid coating and unique physicochemical properties of the core. Some glycosides with hydrophilic sugar moieties bound to oleyl hydrophobic chains have antimitotic activity on cancer cells but reduced in vivo applications because of the intrinsic low solubility in physiological media, and are prone to enzymatic hydrolysis. In this manuscript, we have synthetized and characterized OA-IONP-based micelles encapsulated within amphiphilic bioactive glycosides. The glycoside-coated IONP micelles were tested as Magnetic Resonance Imaging (MRI) contrast agents as well as antimitotics on rat glioma (C6) and human lung carcinoma (A549) cell lines. Micelle antimitotic activity was compared with the activity of the corresponding free glycosides. In general, all OA-IONP-based micellar formulations of these glycosides maintained their anti-tumor effects, and, in one case, showed an unusual therapeutic improvement. Finally, the micelles presented optimal relaxometric properties for their use as T2-weighed MRI contrast agents. Our results suggest that these bioactive hydrophilic nano-formulations are theranostic agents with synergistic properties obtained from two entities, which separately are not ready for in vivo applications, and strengthen the possibility of using biomolecules as both a coating for OA-IONP micellar stabilization and as drugs for therapy.
dc.description.peerreviewed
dc.description.sponsorshipThis research was funded by FP7 Marie Curie Pulmonary imaging network (PINET) and Ministerio de Economia y Competitividad MAT2015-65184-C2-2-R; SAF2016-79593-P; SAF2017-84494-C2-1-R). This work was partially funded by Instituto de Salud Carlos III (DTS16/00059), CNIC (Centro Nacional de Investigaciones Cardiovasculares), and Comunidad de Madrid (B2017-BMD3731 and B2017-BMD3875). We thank Ligue contre le cancer, comite Charentes Maritimes which allows to free up some time to complete the redaction of this manuscript during a grant-not dedicated on this work-agreed to LIENSs, UMR CNRS 7266, La Rochelle.
dc.format.volume8
dc.identifierISI:000443257500006
dc.identifier.citationNanomaterials (Basel). 2018; 8(8):567
dc.identifier.doi10.3390/nano8080567
dc.identifier.issn2079-4991
dc.identifier.journalNanomaterials
dc.identifier.pubmedID30044386
dc.identifier.urihttp://hdl.handle.net/20.500.12105/6541
dc.language.isoeng
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.publisherversionhttps://doi.org/10.3390/nano8080567
dc.repisalud.institucionCNIC
dc.repisalud.orgCNICCNIC::Grupos de investigación
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectGlycoside
dc.subjectIron oxide nanoparticles
dc.subjectNanomicelles
dc.subjectAntitumoral
dc.subjectMULTIFUNCTIONAL MAGNETIC NANOPARTICLES
dc.subjectDRUG-DELIVERY
dc.subjectSUPERPARAMAGNETIC NANOPARTICLES
dc.subjectBIOMEDICAL APPLICATIONS
dc.subjectCONTRAST AGENTS
dc.subjectCANCER-THERAPY
dc.subjectSOLID TUMORS
dc.subjectDIAGNOSIS
dc.subjectNANOTECHNOLOGY
dc.subjectEXPERIENCES
dc.titleMicellar Iron Oxide Nanoparticles Coated with Anti-Tumor Glycosides
dc.typejournal article
dc.type.hasVersionVoR
dspace.entity.typePublication
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relation.isAuthorOfPublicationf0c202e0-8054-4f64-ba3c-a2c107d7cb48
relation.isAuthorOfPublication845644de-01dd-4517-ab89-a07183d31248
relation.isAuthorOfPublication.latestForDiscovery4be0056d-d7df-499d-b5f2-1583e2adcb05

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