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Identification of Nanoparticle Properties for Optimal Drug Delivery across a Physiological Cell Barrier

Nanoparticles (NPs) represent an attractive strategy to overcome difficulties associated with the delivery of therapeutics. Knowing the optimal properties of NPs to address these issues could allow for improved in vivo responses. This work investigated NPs prepared from 5 materials of 3 sizes and 3...

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Detalles Bibliográficos
Autores principales: Ross, Aisling M., Cahalane, Rachel M., Walsh, Darragh R., Grabrucker, Andreas M., Marcar, Lynnette, Mulvihill, John J. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865979/
https://www.ncbi.nlm.nih.gov/pubmed/36678829
http://dx.doi.org/10.3390/pharmaceutics15010200
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author Ross, Aisling M.
Cahalane, Rachel M.
Walsh, Darragh R.
Grabrucker, Andreas M.
Marcar, Lynnette
Mulvihill, John J. E.
author_facet Ross, Aisling M.
Cahalane, Rachel M.
Walsh, Darragh R.
Grabrucker, Andreas M.
Marcar, Lynnette
Mulvihill, John J. E.
author_sort Ross, Aisling M.
collection PubMed
description Nanoparticles (NPs) represent an attractive strategy to overcome difficulties associated with the delivery of therapeutics. Knowing the optimal properties of NPs to address these issues could allow for improved in vivo responses. This work investigated NPs prepared from 5 materials of 3 sizes and 3 concentrations applied to a cell barrier model. The NPs permeability across a cell barrier and their effects on cell barrier integrity and cell viability were evaluated. The properties of these NPs, as determined in water (traditional) vs. media (realistic), were compared to cell responses. It was found that for all cellular activities, NP properties determined in media was the best predictor of the cell response. Notably, ZnO NPs caused significant alterations to cell viability across all 3 cell lines tested. Importantly, we report that the zeta potential of NPs correlates significantly with NP permeability and NP-induced changes in cell viability. NPs with physiological-based zeta potential of −12 mV result in good cell barrier penetration without considerable changes in cell viability.
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spelling pubmed-98659792023-01-22 Identification of Nanoparticle Properties for Optimal Drug Delivery across a Physiological Cell Barrier Ross, Aisling M. Cahalane, Rachel M. Walsh, Darragh R. Grabrucker, Andreas M. Marcar, Lynnette Mulvihill, John J. E. Pharmaceutics Article Nanoparticles (NPs) represent an attractive strategy to overcome difficulties associated with the delivery of therapeutics. Knowing the optimal properties of NPs to address these issues could allow for improved in vivo responses. This work investigated NPs prepared from 5 materials of 3 sizes and 3 concentrations applied to a cell barrier model. The NPs permeability across a cell barrier and their effects on cell barrier integrity and cell viability were evaluated. The properties of these NPs, as determined in water (traditional) vs. media (realistic), were compared to cell responses. It was found that for all cellular activities, NP properties determined in media was the best predictor of the cell response. Notably, ZnO NPs caused significant alterations to cell viability across all 3 cell lines tested. Importantly, we report that the zeta potential of NPs correlates significantly with NP permeability and NP-induced changes in cell viability. NPs with physiological-based zeta potential of −12 mV result in good cell barrier penetration without considerable changes in cell viability. MDPI 2023-01-06 /pmc/articles/PMC9865979/ /pubmed/36678829 http://dx.doi.org/10.3390/pharmaceutics15010200 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ross, Aisling M.
Cahalane, Rachel M.
Walsh, Darragh R.
Grabrucker, Andreas M.
Marcar, Lynnette
Mulvihill, John J. E.
Identification of Nanoparticle Properties for Optimal Drug Delivery across a Physiological Cell Barrier
title Identification of Nanoparticle Properties for Optimal Drug Delivery across a Physiological Cell Barrier
title_full Identification of Nanoparticle Properties for Optimal Drug Delivery across a Physiological Cell Barrier
title_fullStr Identification of Nanoparticle Properties for Optimal Drug Delivery across a Physiological Cell Barrier
title_full_unstemmed Identification of Nanoparticle Properties for Optimal Drug Delivery across a Physiological Cell Barrier
title_short Identification of Nanoparticle Properties for Optimal Drug Delivery across a Physiological Cell Barrier
title_sort identification of nanoparticle properties for optimal drug delivery across a physiological cell barrier
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865979/
https://www.ncbi.nlm.nih.gov/pubmed/36678829
http://dx.doi.org/10.3390/pharmaceutics15010200
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