| Literature DB >> 26875938 |
Cornelia E Peña-González1, Pilar García-Broncano2,3,4,5, M Francesca Ottaviani6, Michela Cangiotti6, Alberto Fattori6, Margarita Hierro-Oliva7,8, M Luisa González-Martín7,8, Jorge Pérez-Serrano9, Rafael Gómez1,8, M Ángeles Muñoz-Fernández3,4,5,8, Javier Sánchez-Nieves10,11, F Javier de la Mata12,13.
Abstract
Anionic carbosilane dendrons decorated with sulfonate functions and one thiol moiety at the focal point have been used to synthesize water-soluble gold nanoparticles (AuNPs) through the direct reaction of dendrons, gold precursor, and reducing agent in water, and also through a place-exchange reaction. These nanoparticles have been characterized by NMR spectroscopy, TEM, thermogravimetric analysis, X-ray photoelectron spectroscopy (XPS), UV/Vis spectroscopy, elemental analysis, and zeta-potential measurements. The interacting ability of the anionic sulfonate functions was investigated by EPR spectroscopy with copper(II) as a probe. Different structures and conformations of the AuNPs modulate the availability of sulfonate and thiol groups for complexation by copper(II). Toxicity assays of AuNPs showed that those produced through direct reaction were less toxic than those obtained by ligand exchange. Inhibition of HIV-1 infection was higher in the case of dendronized AuNPs than in dendrons.Entities:
Keywords: antiviral agents; cytotoxicity; dendrimers; nanoparticles; structure-activity relationships
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Year: 2016 PMID: 26875938 DOI: 10.1002/chem.201504262
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236