Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriers

Cellular barriers, such as the skin, the lung epithelium or the intestinal epithelium, constitute one of the first obstacles facing nanomedicines or other nanoparticles entering organisms. It is thus important to assess the capacity of nanoparticles to enter and transport across such barriers. In th...

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Main Authors: Dong Ye, Mattia Bramini, Delyan R. Hristov, Sha Wan, Anna Salvati, Christoffer Åberg, Kenneth A. Dawson
Format: Article
Language:English
Published: Beilstein-Institut 2017-07-01
Series:Beilstein Journal of Nanotechnology
Subjects:
Online Access:https://doi.org/10.3762/bjnano.8.141
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author Dong Ye
Mattia Bramini
Delyan R. Hristov
Sha Wan
Anna Salvati
Christoffer Åberg
Kenneth A. Dawson
author_facet Dong Ye
Mattia Bramini
Delyan R. Hristov
Sha Wan
Anna Salvati
Christoffer Åberg
Kenneth A. Dawson
author_sort Dong Ye
collection DOAJ
description Cellular barriers, such as the skin, the lung epithelium or the intestinal epithelium, constitute one of the first obstacles facing nanomedicines or other nanoparticles entering organisms. It is thus important to assess the capacity of nanoparticles to enter and transport across such barriers. In this work, Caco-2 intestinal epithelial cells were used as a well-established model for the intestinal barrier, and the uptake, trafficking and translocation of model silica nanoparticles of different sizes were investigated using a combination of imaging, flow cytometry and transport studies. Compared to typical observations in standard cell lines commonly used for in vitro studies, silica nanoparticle uptake into well-developed Caco-2 cellular barriers was found to be very low. Instead, nanoparticle association to the apical outer membrane was substantial and these particles could easily be misinterpreted as internalised in the absence of imaging. Passage of nanoparticles through the barrier was very limited, suggesting that the low amount of internalised nanoparticles was due to reduced uptake into cells, rather than a considerable transport through them.
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spelling doaj.art-5b1e09a842c346b49b9ba8047592cdb42022-12-22T01:48:41ZengBeilstein-InstitutBeilstein Journal of Nanotechnology2190-42862017-07-01811396140610.3762/bjnano.8.1412190-4286-8-141Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriersDong Ye0Mattia Bramini1Delyan R. Hristov2Sha Wan3Anna Salvati4Christoffer Åberg5Kenneth A. Dawson6Centre for BioNano Interactions, School of Chemistry and Chemical Biology, University College Dublin, Belfield, Dublin 4, IrelandCentre for BioNano Interactions, School of Chemistry and Chemical Biology, University College Dublin, Belfield, Dublin 4, IrelandCentre for BioNano Interactions, School of Chemistry and Chemical Biology, University College Dublin, Belfield, Dublin 4, IrelandCentre for BioNano Interactions, School of Chemistry and Chemical Biology, University College Dublin, Belfield, Dublin 4, IrelandCentre for BioNano Interactions, School of Chemistry and Chemical Biology, University College Dublin, Belfield, Dublin 4, IrelandCentre for BioNano Interactions, School of Chemistry and Chemical Biology, University College Dublin, Belfield, Dublin 4, IrelandCentre for BioNano Interactions, School of Chemistry and Chemical Biology, University College Dublin, Belfield, Dublin 4, IrelandCellular barriers, such as the skin, the lung epithelium or the intestinal epithelium, constitute one of the first obstacles facing nanomedicines or other nanoparticles entering organisms. It is thus important to assess the capacity of nanoparticles to enter and transport across such barriers. In this work, Caco-2 intestinal epithelial cells were used as a well-established model for the intestinal barrier, and the uptake, trafficking and translocation of model silica nanoparticles of different sizes were investigated using a combination of imaging, flow cytometry and transport studies. Compared to typical observations in standard cell lines commonly used for in vitro studies, silica nanoparticle uptake into well-developed Caco-2 cellular barriers was found to be very low. Instead, nanoparticle association to the apical outer membrane was substantial and these particles could easily be misinterpreted as internalised in the absence of imaging. Passage of nanoparticles through the barrier was very limited, suggesting that the low amount of internalised nanoparticles was due to reduced uptake into cells, rather than a considerable transport through them.https://doi.org/10.3762/bjnano.8.141Caco-2differentiation and polarisationepithelial cell barriermicroscopy imagingparticle interactionuptake and localisation
spellingShingle Dong Ye
Mattia Bramini
Delyan R. Hristov
Sha Wan
Anna Salvati
Christoffer Åberg
Kenneth A. Dawson
Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriers
Beilstein Journal of Nanotechnology
Caco-2
differentiation and polarisation
epithelial cell barrier
microscopy imaging
particle interaction
uptake and localisation
title Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriers
title_full Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriers
title_fullStr Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriers
title_full_unstemmed Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriers
title_short Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriers
title_sort low uptake of silica nanoparticles in caco 2 intestinal epithelial barriers
topic Caco-2
differentiation and polarisation
epithelial cell barrier
microscopy imaging
particle interaction
uptake and localisation
url https://doi.org/10.3762/bjnano.8.141
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