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Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione

This study was designed to evaluate the nano–bio interactions between endogenous biothiols (cysteine and glutathione) with biomedically relevant, metallic nanoparticles (silver nanoparticles (AgNPs) and gold nanoparticles (AuNPs)), in order to assess the biocompatibility and fate of nanoparticles in...

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Autores principales: Pem, Barbara, Pongrac, Igor M, Ulm, Lea, Pavičić, Ivan, Vrček, Valerije, Domazet Jurašin, Darija, Ljubojević, Marija, Krivohlavek, Adela, Vinković Vrček, Ivana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753685/
https://www.ncbi.nlm.nih.gov/pubmed/31579097
http://dx.doi.org/10.3762/bjnano.10.175
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author Pem, Barbara
Pongrac, Igor M
Ulm, Lea
Pavičić, Ivan
Vrček, Valerije
Domazet Jurašin, Darija
Ljubojević, Marija
Krivohlavek, Adela
Vinković Vrček, Ivana
author_facet Pem, Barbara
Pongrac, Igor M
Ulm, Lea
Pavičić, Ivan
Vrček, Valerije
Domazet Jurašin, Darija
Ljubojević, Marija
Krivohlavek, Adela
Vinković Vrček, Ivana
author_sort Pem, Barbara
collection PubMed
description This study was designed to evaluate the nano–bio interactions between endogenous biothiols (cysteine and glutathione) with biomedically relevant, metallic nanoparticles (silver nanoparticles (AgNPs) and gold nanoparticles (AuNPs)), in order to assess the biocompatibility and fate of nanoparticles in biological systems. A systematic and comprehensive analysis revealed that the preparation of AgNPs and AuNPs in the presence of biothiols leads to nanoparticles stabilized with oxidized forms of biothiols. Their safety was tested by evaluation of cell viability, reactive oxygen species (ROS) production, apoptosis induction and DNA damage in murine fibroblast cells (L929), while ecotoxicity was tested using the aquatic model organism Daphnia magna. The toxicity of these nanoparticles was considerably lower compared to their ionic metal forms (i.e., Ag(+) and Au(3+)). The comparison with data published on polymer-coated nanoparticles evidenced that surface modification with biothiols made them safer for the biological environment. In vitro evaluation on human cells demonstrated that the toxicity of AgNPs and AuNPs prepared in the presence of cysteine was similar to the polymer-based nanoparticles with the same core material, while the use of glutathione for nanoparticle stabilization was considerably less toxic. These results represent a significant contribution to understanding the role of biothiols on the fate and behavior of metal-based nanomaterials.
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spelling pubmed-67536852019-10-02 Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione Pem, Barbara Pongrac, Igor M Ulm, Lea Pavičić, Ivan Vrček, Valerije Domazet Jurašin, Darija Ljubojević, Marija Krivohlavek, Adela Vinković Vrček, Ivana Beilstein J Nanotechnol Full Research Paper This study was designed to evaluate the nano–bio interactions between endogenous biothiols (cysteine and glutathione) with biomedically relevant, metallic nanoparticles (silver nanoparticles (AgNPs) and gold nanoparticles (AuNPs)), in order to assess the biocompatibility and fate of nanoparticles in biological systems. A systematic and comprehensive analysis revealed that the preparation of AgNPs and AuNPs in the presence of biothiols leads to nanoparticles stabilized with oxidized forms of biothiols. Their safety was tested by evaluation of cell viability, reactive oxygen species (ROS) production, apoptosis induction and DNA damage in murine fibroblast cells (L929), while ecotoxicity was tested using the aquatic model organism Daphnia magna. The toxicity of these nanoparticles was considerably lower compared to their ionic metal forms (i.e., Ag(+) and Au(3+)). The comparison with data published on polymer-coated nanoparticles evidenced that surface modification with biothiols made them safer for the biological environment. In vitro evaluation on human cells demonstrated that the toxicity of AgNPs and AuNPs prepared in the presence of cysteine was similar to the polymer-based nanoparticles with the same core material, while the use of glutathione for nanoparticle stabilization was considerably less toxic. These results represent a significant contribution to understanding the role of biothiols on the fate and behavior of metal-based nanomaterials. Beilstein-Institut 2019-09-02 /pmc/articles/PMC6753685/ /pubmed/31579097 http://dx.doi.org/10.3762/bjnano.10.175 Text en Copyright © 2019, Pem et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjnano/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Nanotechnology terms and conditions: (https://www.beilstein-journals.org/bjnano/terms)
spellingShingle Full Research Paper
Pem, Barbara
Pongrac, Igor M
Ulm, Lea
Pavičić, Ivan
Vrček, Valerije
Domazet Jurašin, Darija
Ljubojević, Marija
Krivohlavek, Adela
Vinković Vrček, Ivana
Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione
title Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione
title_full Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione
title_fullStr Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione
title_full_unstemmed Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione
title_short Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione
title_sort toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753685/
https://www.ncbi.nlm.nih.gov/pubmed/31579097
http://dx.doi.org/10.3762/bjnano.10.175
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