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Authordc.contributor.authorMorales Zavala, Francisco 
Authordc.contributor.authorArriagada, Hector 
Authordc.contributor.authorHassan, Natalia 
Authordc.contributor.authorVelasco, Carolina 
Authordc.contributor.authorRiveros Salvatierra, Ana 
Authordc.contributor.authorÁlvarez, Alejandra R. 
Authordc.contributor.authorMinniti, Alicia N. 
Authordc.contributor.authorRojas Silva, Ximena 
Authordc.contributor.authorMunoz, Luis L. 
Authordc.contributor.authorVásquez Salfate, Rodrigo 
Authordc.contributor.authorRodríguez, Katherine 
Authordc.contributor.authorSánchez Navarro, Macarena 
Authordc.contributor.authorGiralt, Ernest 
Authordc.contributor.authorAraya, Eyleen 
Authordc.contributor.authorAldunate, Rebeca 
Authordc.contributor.authorKogan Bocian, Marcelo 
Admission datedc.date.accessioned2018-06-29T19:46:32Z
Available datedc.date.available2018-06-29T19:46:32Z
Publication datedc.date.issued2017
Cita de ítemdc.identifier.citationNanomedicine: Nanotechnology, Biology, and Medicine, 13 (2017): 2341–2350es_ES
Identifierdc.identifier.other10.1016/j.nano.2017.06.013
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/149370
Abstractdc.description.abstractThe properties of nanometric materials make nanotechnology a promising platform for tackling problems of contemporary medicine. In this work, gold nanorods were synthetized and stabilized with polyethylene glycols and modified with two kinds of peptides. The D1 peptide that recognizes toxic aggregates of A beta, a peptide involved in Alzheimer's disease (AD); and the Angiopep 2 that can be used to deliver nanorods to the mammalian central nervous system. The nanoconjugates were characterized using absorption spectrophotometry, dynamic light scattering, and transmission electron microscopy, among other techniques. We determined that the nanoconjugate does not affect neuronal viability; it penetrates the cells, and decreases aggregation of A beta peptide in vitro. We also showed that when we apply our nanosystem to a Caenorhabditis elegans AD model, the toxicity of aggregated A beta peptide is decreased. This work may contribute to the development of therapies for AD based on metallic nanoparticles.es_ES
Patrocinadordc.description.sponsorshipFondecyt 1130425 11130494 1170929 Fondap 15130011 Proyecto Interno UST Proyecto DI 1609/16R Programa Fondecyt Postdoctoral 3140489 Beca CONICYT Doctorado Nacional 21120617es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherElsevieres_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceNanomedicine: Nanotechnology, Biology, and Medicinees_ES
Keywordsdc.subjectGold nanoparticlees_ES
Keywordsdc.subjectGold nanorodses_ES
Keywordsdc.subjectAmyloid beta peptidees_ES
Keywordsdc.subjectAlzheimer's nanotherapyes_ES
Keywordsdc.subjectDrug deliveryes_ES
Títulodc.titlePeptide multifunctionalized gold nanorods decrease toxicity of beta-amyloid peptide in a Caenorhabditis elegans model of Alzheimer's diseasees_ES
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadortjnes_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile