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Important factors for cell-membrane permeabilization by gold nanoparticles activated by nanosecond-laser irradiation
PURPOSE: Pulsed-laser irradiation of light-absorbing gold nanoparticles (AuNPs) attached to cells transiently increases cell membrane permeability for targeted molecule delivery. Here, we targeted EGFR on the ovarian carcinoma cell line OVCAR-3 with AuNPs. In order to optimize membrane permeability...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557627/ https://www.ncbi.nlm.nih.gov/pubmed/28848345 http://dx.doi.org/10.2147/IJN.S140620 |
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author | Yao, Cuiping Rudnitzki, Florian Hüttmann, Gereon Zhang, Zhenxi Rahmanzadeh, Ramtin |
author_facet | Yao, Cuiping Rudnitzki, Florian Hüttmann, Gereon Zhang, Zhenxi Rahmanzadeh, Ramtin |
author_sort | Yao, Cuiping |
collection | PubMed |
description | PURPOSE: Pulsed-laser irradiation of light-absorbing gold nanoparticles (AuNPs) attached to cells transiently increases cell membrane permeability for targeted molecule delivery. Here, we targeted EGFR on the ovarian carcinoma cell line OVCAR-3 with AuNPs. In order to optimize membrane permeability and to demonstrate molecule delivery into adherent OVCAR-3 cells, we systematically investigated different experimental conditions. MATERIALS AND METHODS: AuNPs (30 nm) were functionalized by conjugation of the antibody cetuximab against EGFR. Selective binding of the particles was demonstrated by silver staining, multiphoton imaging, and fluorescence-lifetime imaging. After laser irradiation, membrane permeability of OVCAR-3 cells was studied under different conditions of AuNP concentration, cell-incubation medium, and cell–AuNP incubation time. Membrane permeability and cell viability were evaluated by flow cytometry, measuring propidium iodide and fluorescein isothiocyanate–dextran uptake. RESULTS: Adherently growing OVCAR-3 cells can be effectively targeted with EGFR-AuNP. Laser irradiation led to successful permeabilization, and 150 kDa dextran was successfully delivered into cells with about 70% efficiency. CONCLUSION: Antibody-targeted and laser-irradiated AuNPs can be used to deliver molecules into adherent cells. Efficacy depends not only on laser parameters but also on AuNP:cell ratio, cell-incubation medium, and cell–AuNP incubation time. |
format | Online Article Text |
id | pubmed-5557627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55576272017-08-28 Important factors for cell-membrane permeabilization by gold nanoparticles activated by nanosecond-laser irradiation Yao, Cuiping Rudnitzki, Florian Hüttmann, Gereon Zhang, Zhenxi Rahmanzadeh, Ramtin Int J Nanomedicine Methodology PURPOSE: Pulsed-laser irradiation of light-absorbing gold nanoparticles (AuNPs) attached to cells transiently increases cell membrane permeability for targeted molecule delivery. Here, we targeted EGFR on the ovarian carcinoma cell line OVCAR-3 with AuNPs. In order to optimize membrane permeability and to demonstrate molecule delivery into adherent OVCAR-3 cells, we systematically investigated different experimental conditions. MATERIALS AND METHODS: AuNPs (30 nm) were functionalized by conjugation of the antibody cetuximab against EGFR. Selective binding of the particles was demonstrated by silver staining, multiphoton imaging, and fluorescence-lifetime imaging. After laser irradiation, membrane permeability of OVCAR-3 cells was studied under different conditions of AuNP concentration, cell-incubation medium, and cell–AuNP incubation time. Membrane permeability and cell viability were evaluated by flow cytometry, measuring propidium iodide and fluorescein isothiocyanate–dextran uptake. RESULTS: Adherently growing OVCAR-3 cells can be effectively targeted with EGFR-AuNP. Laser irradiation led to successful permeabilization, and 150 kDa dextran was successfully delivered into cells with about 70% efficiency. CONCLUSION: Antibody-targeted and laser-irradiated AuNPs can be used to deliver molecules into adherent cells. Efficacy depends not only on laser parameters but also on AuNP:cell ratio, cell-incubation medium, and cell–AuNP incubation time. Dove Medical Press 2017-08-07 /pmc/articles/PMC5557627/ /pubmed/28848345 http://dx.doi.org/10.2147/IJN.S140620 Text en © 2017 Yao et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Methodology Yao, Cuiping Rudnitzki, Florian Hüttmann, Gereon Zhang, Zhenxi Rahmanzadeh, Ramtin Important factors for cell-membrane permeabilization by gold nanoparticles activated by nanosecond-laser irradiation |
title | Important factors for cell-membrane permeabilization by gold nanoparticles activated by nanosecond-laser irradiation |
title_full | Important factors for cell-membrane permeabilization by gold nanoparticles activated by nanosecond-laser irradiation |
title_fullStr | Important factors for cell-membrane permeabilization by gold nanoparticles activated by nanosecond-laser irradiation |
title_full_unstemmed | Important factors for cell-membrane permeabilization by gold nanoparticles activated by nanosecond-laser irradiation |
title_short | Important factors for cell-membrane permeabilization by gold nanoparticles activated by nanosecond-laser irradiation |
title_sort | important factors for cell-membrane permeabilization by gold nanoparticles activated by nanosecond-laser irradiation |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557627/ https://www.ncbi.nlm.nih.gov/pubmed/28848345 http://dx.doi.org/10.2147/IJN.S140620 |
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