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Porous Carbon Microparticles as Vehicles for the Intracellular Delivery of Molecules

In this study the application of porous carbon microparticles for the transport of a sparingly soluble material into cells is demonstrated. Carbon offers an intrinsically sustainable platform material that can meet the multiple and complex requirements imposed by applications in biology and medicine...

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Autores principales: Magno, Luis M., Hinds, David T., Duffy, Paul, Yadav, Rahul. B., Ward, Andrew D., Botchway, Stan W., Colavita, Paula E., Quinn, Susan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591791/
https://www.ncbi.nlm.nih.gov/pubmed/33195066
http://dx.doi.org/10.3389/fchem.2020.576175
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author Magno, Luis M.
Hinds, David T.
Duffy, Paul
Yadav, Rahul. B.
Ward, Andrew D.
Botchway, Stan W.
Colavita, Paula E.
Quinn, Susan J.
author_facet Magno, Luis M.
Hinds, David T.
Duffy, Paul
Yadav, Rahul. B.
Ward, Andrew D.
Botchway, Stan W.
Colavita, Paula E.
Quinn, Susan J.
author_sort Magno, Luis M.
collection PubMed
description In this study the application of porous carbon microparticles for the transport of a sparingly soluble material into cells is demonstrated. Carbon offers an intrinsically sustainable platform material that can meet the multiple and complex requirements imposed by applications in biology and medicine. Porous carbon microparticles are attractive as they are easy to handle and manipulate and combine the chemical versatility and biocompatibility of carbon with a high surface area due to their highly porous structure. The uptake of fluorescently labeled microparticles by cancer (HeLa) and normal human embryonic Kidney (HEK 293) cells was monitored by confocal fluorescence microscopy. In this way the influence of particle size, surface functionalization and the presence of transfection agent on cellular uptake were studied. In the presence of transfection agent both large (690 nm) and small microparticles (250 nm) were readily internalized by both cell lines. However, in absence of the transfection agent the uptake was influenced by particle size and surface PEGylation with the smaller nanoparticle size being delivered. The ability of microparticles to deliver a fluorescein dye model cargo was also demonstrated in normal (HEK 293) cell line. Taken together, these results indicate the potential use of these materials as candidates for biological applications.
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spelling pubmed-75917912020-11-13 Porous Carbon Microparticles as Vehicles for the Intracellular Delivery of Molecules Magno, Luis M. Hinds, David T. Duffy, Paul Yadav, Rahul. B. Ward, Andrew D. Botchway, Stan W. Colavita, Paula E. Quinn, Susan J. Front Chem Chemistry In this study the application of porous carbon microparticles for the transport of a sparingly soluble material into cells is demonstrated. Carbon offers an intrinsically sustainable platform material that can meet the multiple and complex requirements imposed by applications in biology and medicine. Porous carbon microparticles are attractive as they are easy to handle and manipulate and combine the chemical versatility and biocompatibility of carbon with a high surface area due to their highly porous structure. The uptake of fluorescently labeled microparticles by cancer (HeLa) and normal human embryonic Kidney (HEK 293) cells was monitored by confocal fluorescence microscopy. In this way the influence of particle size, surface functionalization and the presence of transfection agent on cellular uptake were studied. In the presence of transfection agent both large (690 nm) and small microparticles (250 nm) were readily internalized by both cell lines. However, in absence of the transfection agent the uptake was influenced by particle size and surface PEGylation with the smaller nanoparticle size being delivered. The ability of microparticles to deliver a fluorescein dye model cargo was also demonstrated in normal (HEK 293) cell line. Taken together, these results indicate the potential use of these materials as candidates for biological applications. Frontiers Media S.A. 2020-10-14 /pmc/articles/PMC7591791/ /pubmed/33195066 http://dx.doi.org/10.3389/fchem.2020.576175 Text en Copyright © 2020 Magno, Hinds, Duffy, Yadav, Ward, Botchway, Colavita and Quinn. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Magno, Luis M.
Hinds, David T.
Duffy, Paul
Yadav, Rahul. B.
Ward, Andrew D.
Botchway, Stan W.
Colavita, Paula E.
Quinn, Susan J.
Porous Carbon Microparticles as Vehicles for the Intracellular Delivery of Molecules
title Porous Carbon Microparticles as Vehicles for the Intracellular Delivery of Molecules
title_full Porous Carbon Microparticles as Vehicles for the Intracellular Delivery of Molecules
title_fullStr Porous Carbon Microparticles as Vehicles for the Intracellular Delivery of Molecules
title_full_unstemmed Porous Carbon Microparticles as Vehicles for the Intracellular Delivery of Molecules
title_short Porous Carbon Microparticles as Vehicles for the Intracellular Delivery of Molecules
title_sort porous carbon microparticles as vehicles for the intracellular delivery of molecules
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591791/
https://www.ncbi.nlm.nih.gov/pubmed/33195066
http://dx.doi.org/10.3389/fchem.2020.576175
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