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Quantification of the internalization patterns of superparamagnetic iron oxide nanoparticles with opposite charge

Time-resolved quantitative colocalization analysis is a method based on confocal fluorescence microscopy allowing for a sophisticated characterization of nanomaterials with respect to their intracellular trafficking. This technique was applied to relate the internalization patterns of nanoparticles...

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Autores principales: Schweiger, Christoph, Hartmann, Raimo, Zhang, Feng, Parak, Wolfgang J, Kissel, Thomas H, Rivera_Gil, Pilar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431280/
https://www.ncbi.nlm.nih.gov/pubmed/22781560
http://dx.doi.org/10.1186/1477-3155-10-28
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author Schweiger, Christoph
Hartmann, Raimo
Zhang, Feng
Parak, Wolfgang J
Kissel, Thomas H
Rivera_Gil, Pilar
author_facet Schweiger, Christoph
Hartmann, Raimo
Zhang, Feng
Parak, Wolfgang J
Kissel, Thomas H
Rivera_Gil, Pilar
author_sort Schweiger, Christoph
collection PubMed
description Time-resolved quantitative colocalization analysis is a method based on confocal fluorescence microscopy allowing for a sophisticated characterization of nanomaterials with respect to their intracellular trafficking. This technique was applied to relate the internalization patterns of nanoparticles i.e. superparamagnetic iron oxide nanoparticles with distinct physicochemical characteristics with their uptake mechanism, rate and intracellular fate. The physicochemical characterization of the nanoparticles showed particles of approximately the same size and shape as well as similar magnetic properties, only differing in charge due to different surface coatings. Incubation of the cells with both nanoparticles resulted in strong differences in the internalization rate and in the intracellular localization depending on the charge. Quantitative and qualitative analysis of nanoparticles-organelle colocalization experiments revealed that positively charged particles were found to enter the cells faster using different endocytotic pathways than their negative counterparts. Nevertheless, both nanoparticles species were finally enriched inside lysosomal structures and their efficiency in agarose phantom relaxometry experiments was very similar. This quantitative analysis demonstrates that charge is a key factor influencing the nanoparticle-cell interactions, specially their intracellular accumulation. Despite differences in their physicochemical properties and intracellular distribution, the efficiencies of both nanoparticles as MRI agents were not significantly different.
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spelling pubmed-34312802012-09-05 Quantification of the internalization patterns of superparamagnetic iron oxide nanoparticles with opposite charge Schweiger, Christoph Hartmann, Raimo Zhang, Feng Parak, Wolfgang J Kissel, Thomas H Rivera_Gil, Pilar J Nanobiotechnology Research Time-resolved quantitative colocalization analysis is a method based on confocal fluorescence microscopy allowing for a sophisticated characterization of nanomaterials with respect to their intracellular trafficking. This technique was applied to relate the internalization patterns of nanoparticles i.e. superparamagnetic iron oxide nanoparticles with distinct physicochemical characteristics with their uptake mechanism, rate and intracellular fate. The physicochemical characterization of the nanoparticles showed particles of approximately the same size and shape as well as similar magnetic properties, only differing in charge due to different surface coatings. Incubation of the cells with both nanoparticles resulted in strong differences in the internalization rate and in the intracellular localization depending on the charge. Quantitative and qualitative analysis of nanoparticles-organelle colocalization experiments revealed that positively charged particles were found to enter the cells faster using different endocytotic pathways than their negative counterparts. Nevertheless, both nanoparticles species were finally enriched inside lysosomal structures and their efficiency in agarose phantom relaxometry experiments was very similar. This quantitative analysis demonstrates that charge is a key factor influencing the nanoparticle-cell interactions, specially their intracellular accumulation. Despite differences in their physicochemical properties and intracellular distribution, the efficiencies of both nanoparticles as MRI agents were not significantly different. BioMed Central 2012-07-10 /pmc/articles/PMC3431280/ /pubmed/22781560 http://dx.doi.org/10.1186/1477-3155-10-28 Text en Copyright ©2012 Schweiger et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Schweiger, Christoph
Hartmann, Raimo
Zhang, Feng
Parak, Wolfgang J
Kissel, Thomas H
Rivera_Gil, Pilar
Quantification of the internalization patterns of superparamagnetic iron oxide nanoparticles with opposite charge
title Quantification of the internalization patterns of superparamagnetic iron oxide nanoparticles with opposite charge
title_full Quantification of the internalization patterns of superparamagnetic iron oxide nanoparticles with opposite charge
title_fullStr Quantification of the internalization patterns of superparamagnetic iron oxide nanoparticles with opposite charge
title_full_unstemmed Quantification of the internalization patterns of superparamagnetic iron oxide nanoparticles with opposite charge
title_short Quantification of the internalization patterns of superparamagnetic iron oxide nanoparticles with opposite charge
title_sort quantification of the internalization patterns of superparamagnetic iron oxide nanoparticles with opposite charge
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431280/
https://www.ncbi.nlm.nih.gov/pubmed/22781560
http://dx.doi.org/10.1186/1477-3155-10-28
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