Peptide multifunctionalized gold nanorods decrease toxicity of beta-amyloid peptide in a Caenorhabditis elegans model of Alzheimer's disease
Author
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Morales Zavala, Francisco
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Arriagada, Hector
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Hassan, Natalia
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Velasco, Carolina
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Riveros Salvatierra, Ana
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Álvarez, Alejandra R.
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Minniti, Alicia N.
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Rojas Silva, Ximena
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Munoz, Luis L.
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Vásquez Salfate, Rodrigo
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Rodríguez, Katherine
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Sánchez Navarro, Macarena
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Giralt, Ernest
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Araya, Eyleen
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Aldunate, Rebeca
Author
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Kogan Bocian, Marcelo
Admission date
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2018-06-29T19:46:32Z
Available date
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2018-06-29T19:46:32Z
Publication date
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2017
Cita de ítem
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Nanomedicine: Nanotechnology, Biology, and Medicine, 13 (2017): 2341–2350
es_ES
Identifier
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10.1016/j.nano.2017.06.013
Identifier
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https://repositorio.uchile.cl/handle/2250/149370
Abstract
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The 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
Patrocinador
dc.description.sponsorship
Fondecyt
1130425
11130494
1170929
Fondap
15130011
Proyecto Interno UST
Proyecto
DI 1609/16R
Programa Fondecyt Postdoctoral
3140489
Beca CONICYT Doctorado Nacional
21120617