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Uptake and Intracellular Trafficking Studies of Multiple Dye-Doped Core-Shell Silica Nanoparticles in Lymphoid and Myeloid Cells

INTRODUCTION: Since most biologically active macromolecules are natural nanostructures, operating in the same scale of biomolecules gives the great advantage to enhance the interaction with cellular components. Noteworthy efforts in nanotechnology, particularly in biomedical and pharmaceutical field...

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Autores principales: Sola, Federica, Canonico, Barbara, Montanari, Mariele, Volpe, Angela, Barattini, Chiara, Pellegrino, Chiara, Cesarini, Erica, Guescini, Michele, Battistelli, Michela, Ortolani, Claudio, Ventola, Alfredo, Papa, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954439/
https://www.ncbi.nlm.nih.gov/pubmed/33727804
http://dx.doi.org/10.2147/NSA.S290867
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author Sola, Federica
Canonico, Barbara
Montanari, Mariele
Volpe, Angela
Barattini, Chiara
Pellegrino, Chiara
Cesarini, Erica
Guescini, Michele
Battistelli, Michela
Ortolani, Claudio
Ventola, Alfredo
Papa, Stefano
author_facet Sola, Federica
Canonico, Barbara
Montanari, Mariele
Volpe, Angela
Barattini, Chiara
Pellegrino, Chiara
Cesarini, Erica
Guescini, Michele
Battistelli, Michela
Ortolani, Claudio
Ventola, Alfredo
Papa, Stefano
author_sort Sola, Federica
collection PubMed
description INTRODUCTION: Since most biologically active macromolecules are natural nanostructures, operating in the same scale of biomolecules gives the great advantage to enhance the interaction with cellular components. Noteworthy efforts in nanotechnology, particularly in biomedical and pharmaceutical fields, have propelled a high number of studies on the biological effects of nanomaterials. Moreover, the determination of specific physicochemical properties of nanomaterials is crucial for the evaluation and design of novel safe and efficient therapeutics and diagnostic tools. In this in vitro study, we report a physicochemical characterisation of fluorescent silica nanoparticles (NPs), interacting with biological models (U937 and PBMC cells), describing the specific triggered biologic response. METHODS: Flow Cytometric and Confocal analyses are the main method platforms. However TEM, NTA, DLS, and chemical procedures to synthesize NPs were employed. RESULTS: NT(B)700 NPs, employed in this study, are fluorescent core-shell silica nanoparticles, synthesized through a micelle-assisted method, where the fluorescence energy transfer process, known as FRET, occurs at a high efficiency rate. Using flow cytometry and confocal microscopy, we observed that NT(B)700 NP uptake seemed to be a rapid, concentration-, energy- and cell type-dependent process, which did not induce significant cytotoxic effects. We did not observe a preferred route of internalization, although their size and the possible aggregated state could influence their extrusion. At this level of analysis, our investigation focuses on lysosome and mitochondria pathways, highlighting that both are involved in NP co-localization. Despite the main mitochondria localization, NPs did not induce a significant increase of intracellular ROS, known inductors of apoptosis, during the time course of analyses. Finally, both lymphoid and myeloid cells are able to release NPs, essential to their biosafety. DISCUSSION: These data allow to consider NT(B)700 NPs a promising platform for future development of a multifunctional system, by combining imaging and localized therapeutic applications in a unique tool.
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spelling pubmed-79544392021-03-15 Uptake and Intracellular Trafficking Studies of Multiple Dye-Doped Core-Shell Silica Nanoparticles in Lymphoid and Myeloid Cells Sola, Federica Canonico, Barbara Montanari, Mariele Volpe, Angela Barattini, Chiara Pellegrino, Chiara Cesarini, Erica Guescini, Michele Battistelli, Michela Ortolani, Claudio Ventola, Alfredo Papa, Stefano Nanotechnol Sci Appl Original Research INTRODUCTION: Since most biologically active macromolecules are natural nanostructures, operating in the same scale of biomolecules gives the great advantage to enhance the interaction with cellular components. Noteworthy efforts in nanotechnology, particularly in biomedical and pharmaceutical fields, have propelled a high number of studies on the biological effects of nanomaterials. Moreover, the determination of specific physicochemical properties of nanomaterials is crucial for the evaluation and design of novel safe and efficient therapeutics and diagnostic tools. In this in vitro study, we report a physicochemical characterisation of fluorescent silica nanoparticles (NPs), interacting with biological models (U937 and PBMC cells), describing the specific triggered biologic response. METHODS: Flow Cytometric and Confocal analyses are the main method platforms. However TEM, NTA, DLS, and chemical procedures to synthesize NPs were employed. RESULTS: NT(B)700 NPs, employed in this study, are fluorescent core-shell silica nanoparticles, synthesized through a micelle-assisted method, where the fluorescence energy transfer process, known as FRET, occurs at a high efficiency rate. Using flow cytometry and confocal microscopy, we observed that NT(B)700 NP uptake seemed to be a rapid, concentration-, energy- and cell type-dependent process, which did not induce significant cytotoxic effects. We did not observe a preferred route of internalization, although their size and the possible aggregated state could influence their extrusion. At this level of analysis, our investigation focuses on lysosome and mitochondria pathways, highlighting that both are involved in NP co-localization. Despite the main mitochondria localization, NPs did not induce a significant increase of intracellular ROS, known inductors of apoptosis, during the time course of analyses. Finally, both lymphoid and myeloid cells are able to release NPs, essential to their biosafety. DISCUSSION: These data allow to consider NT(B)700 NPs a promising platform for future development of a multifunctional system, by combining imaging and localized therapeutic applications in a unique tool. Dove 2021-03-08 /pmc/articles/PMC7954439/ /pubmed/33727804 http://dx.doi.org/10.2147/NSA.S290867 Text en © 2021 Sola et al. http://creativecommons.org/licenses/by-nc/3.0/ 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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Sola, Federica
Canonico, Barbara
Montanari, Mariele
Volpe, Angela
Barattini, Chiara
Pellegrino, Chiara
Cesarini, Erica
Guescini, Michele
Battistelli, Michela
Ortolani, Claudio
Ventola, Alfredo
Papa, Stefano
Uptake and Intracellular Trafficking Studies of Multiple Dye-Doped Core-Shell Silica Nanoparticles in Lymphoid and Myeloid Cells
title Uptake and Intracellular Trafficking Studies of Multiple Dye-Doped Core-Shell Silica Nanoparticles in Lymphoid and Myeloid Cells
title_full Uptake and Intracellular Trafficking Studies of Multiple Dye-Doped Core-Shell Silica Nanoparticles in Lymphoid and Myeloid Cells
title_fullStr Uptake and Intracellular Trafficking Studies of Multiple Dye-Doped Core-Shell Silica Nanoparticles in Lymphoid and Myeloid Cells
title_full_unstemmed Uptake and Intracellular Trafficking Studies of Multiple Dye-Doped Core-Shell Silica Nanoparticles in Lymphoid and Myeloid Cells
title_short Uptake and Intracellular Trafficking Studies of Multiple Dye-Doped Core-Shell Silica Nanoparticles in Lymphoid and Myeloid Cells
title_sort uptake and intracellular trafficking studies of multiple dye-doped core-shell silica nanoparticles in lymphoid and myeloid cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954439/
https://www.ncbi.nlm.nih.gov/pubmed/33727804
http://dx.doi.org/10.2147/NSA.S290867
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