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An Integrated In Vitro–In Silico Approach for Silver Nanoparticle Dosimetry in Cell Cultures

Potential human and environmental hazards resulting from the exposure of living organisms to silver nanoparticles (Ag NPs) have been the subject of intensive discussion in the last decade. Despite the growing use of Ag NPs in biomedical applications, a quantification of the toxic effects as a functi...

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Autores principales: Poli, Daniele, Mattei, Giorgio, Ucciferri, Nadia, Ahluwalia, Arti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089903/
https://www.ncbi.nlm.nih.gov/pubmed/31933000
http://dx.doi.org/10.1007/s10439-020-02449-5
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author Poli, Daniele
Mattei, Giorgio
Ucciferri, Nadia
Ahluwalia, Arti
author_facet Poli, Daniele
Mattei, Giorgio
Ucciferri, Nadia
Ahluwalia, Arti
author_sort Poli, Daniele
collection PubMed
description Potential human and environmental hazards resulting from the exposure of living organisms to silver nanoparticles (Ag NPs) have been the subject of intensive discussion in the last decade. Despite the growing use of Ag NPs in biomedical applications, a quantification of the toxic effects as a function of the total silver mass reaching cells (namely, target cell dose) is still needed. To provide a more accurate dose-response analysis, we propose a novel integrated approach combining well-established computational and experimental methodologies. We first used a particokinetic model (ISD3) for providing experimental validation of computed Ag NP sedimentation in static-cuvette experiments. After validation, ISD3 was employed to predict the total mass of silver reaching human endothelial cells and hepatocytes cultured in 96 well plates. Cell viability measured after 24 h of culture was then related to this target cell dose. Our results show that the dose perceived by the cell monolayer after 24 h of exposure is around 85% lower than the administered nominal media concentration. Therefore, accurate dosimetry considering particle characteristics and experimental conditions (e.g., time, size and shape of wells) should be employed for better interpreting effects induced by the amount of silver reaching cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10439-020-02449-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-70899032020-03-26 An Integrated In Vitro–In Silico Approach for Silver Nanoparticle Dosimetry in Cell Cultures Poli, Daniele Mattei, Giorgio Ucciferri, Nadia Ahluwalia, Arti Ann Biomed Eng Original Article Potential human and environmental hazards resulting from the exposure of living organisms to silver nanoparticles (Ag NPs) have been the subject of intensive discussion in the last decade. Despite the growing use of Ag NPs in biomedical applications, a quantification of the toxic effects as a function of the total silver mass reaching cells (namely, target cell dose) is still needed. To provide a more accurate dose-response analysis, we propose a novel integrated approach combining well-established computational and experimental methodologies. We first used a particokinetic model (ISD3) for providing experimental validation of computed Ag NP sedimentation in static-cuvette experiments. After validation, ISD3 was employed to predict the total mass of silver reaching human endothelial cells and hepatocytes cultured in 96 well plates. Cell viability measured after 24 h of culture was then related to this target cell dose. Our results show that the dose perceived by the cell monolayer after 24 h of exposure is around 85% lower than the administered nominal media concentration. Therefore, accurate dosimetry considering particle characteristics and experimental conditions (e.g., time, size and shape of wells) should be employed for better interpreting effects induced by the amount of silver reaching cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10439-020-02449-5) contains supplementary material, which is available to authorized users. Springer International Publishing 2020-01-13 2020 /pmc/articles/PMC7089903/ /pubmed/31933000 http://dx.doi.org/10.1007/s10439-020-02449-5 Text en © The Author(s) 2020, corrected publication 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Poli, Daniele
Mattei, Giorgio
Ucciferri, Nadia
Ahluwalia, Arti
An Integrated In Vitro–In Silico Approach for Silver Nanoparticle Dosimetry in Cell Cultures
title An Integrated In Vitro–In Silico Approach for Silver Nanoparticle Dosimetry in Cell Cultures
title_full An Integrated In Vitro–In Silico Approach for Silver Nanoparticle Dosimetry in Cell Cultures
title_fullStr An Integrated In Vitro–In Silico Approach for Silver Nanoparticle Dosimetry in Cell Cultures
title_full_unstemmed An Integrated In Vitro–In Silico Approach for Silver Nanoparticle Dosimetry in Cell Cultures
title_short An Integrated In Vitro–In Silico Approach for Silver Nanoparticle Dosimetry in Cell Cultures
title_sort integrated in vitro–in silico approach for silver nanoparticle dosimetry in cell cultures
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089903/
https://www.ncbi.nlm.nih.gov/pubmed/31933000
http://dx.doi.org/10.1007/s10439-020-02449-5
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