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Short-chain PEG molecules strongly bound to magnetic nanoparticle for MRI long circulating agents

dc.contributor.authorRuiz, Amalia
dc.contributor.authorSalas, Gorka
dc.contributor.authorCalero Calero, Macarena
dc.contributor.authorHernández, Yurena
dc.contributor.authorVillanueva, Angeles
dc.contributor.authorHerranz, Fernando
dc.contributor.authorBarber, Domingo F
dc.contributor.authorMorales, María del Puerto
dc.date.accessioned2024-01-15T17:06:07Z
dc.date.available2024-01-15T17:06:07Z
dc.date.issued2013
dc.description.abstractThis study developed an approach for the synthesis of magnetic nanoparticles coated with three different polyethylene glycol (PEG)-derived molecules. The influence of the coating on different properties of the nanoparticles was studied. Magnetite nanoparticles (7 and 12 nm in diameter) were obtained via thermal decomposition of a coordination complex as an iron precursor to ensure nanoparticle homogeneity in size and shape. Particles were first coated with meso-2,3-dimercaptosuccinic acid by a ligand exchange process to remove oleic acid, followed by modification with three distinct short-chain PEG polymers, which were covalently bound to the nanoparticle surface via 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride activation of the carboxylic acids. In all cases, colloidal suspensions had hydrodynamic sizes <100 nm and low surface charge, demonstrating the effect of PEG coating on the aggregation properties and steric stabilization of the magnetic nanoparticles. The internalization and biocompatibility of these materials in the HeLa human cervical carcinoma cell line were tested. Cells preincubated with PEG-coated iron nanoparticles were visualized outside the cells, and their biocompatibility at high Fe concentrations was demonstrated using a standard 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay. Finally, relaxivity parameters (r1 and r2) were used to evaluate the efficiency of suspensions as magnetic resonance imaging contrast agents; the r2 value was similar to that for Resovist and up to four times higher than that for Sinerem, probably due to the larger nanoparticle size. The time of residence in blood of the nanoparticles measured from the relaxivity values, and the Fe content in blood was doubled for rats and rabbits due to the PEG on the nanoparticle surface. The results suggest that this PEGylation strategy for large magnetic nanoparticles (>10 nm) holds promise for biomedical applications.
dc.description.departmentDepto. de Química Física
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (España)
dc.description.sponsorshipComunidad de Madrid
dc.description.statuspub
dc.identifier.citationRuiz, A.; Salas, G.; Calero, M.; Hernández, Y.; Villanueva, A.; Herranz, F.; Veintemillas-Verdaguer, S.; Martínez, E.; Barber, D. F.; Morales, M. P. Short-chain PEG molecules strongly bound to magnetic nanoparticle for MRI long circulating agents. Acta Biomaterialia 2013, 9, 6421-6430 DOI:10.1016/j.actbio.2012.12.032.
dc.identifier.doi10.1016/j.actbio.2012.12.032
dc.identifier.issn1742-7061
dc.identifier.officialurlhttps://www.doi.org/10.1016/j.actbio.2012.12.032
dc.identifier.urihttps://hdl.handle.net/20.500.14352/93191
dc.issue.number5
dc.journal.titleActa Biomaterialia
dc.language.isoeng
dc.page.final6430
dc.page.initial6421
dc.publisherElsevier
dc.rights.accessRightsrestricted access
dc.subject.cdu544
dc.subject.ucmCiencias
dc.subject.unesco23 Química
dc.titleShort-chain PEG molecules strongly bound to magnetic nanoparticle for MRI long circulating agents
dc.typejournal article
dc.volume.number9
dspace.entity.typePublication
relation.isAuthorOfPublication05905ac6-6715-42b9-aecf-299d305e882c
relation.isAuthorOfPublication.latestForDiscovery05905ac6-6715-42b9-aecf-299d305e882c

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