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

Federica Sola,1,2 Barbara Canonico,1 Mariele Montanari,1 Angela Volpe,2 Chiara Barattini,1,2 Chiara Pellegrino,2 Erica Cesarini,1 Michele Guescini,1 Michela Battistelli,1 Claudio Ortolani,1 Alfredo Ventola,2 Stefano Papa1 1Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, P...

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Main Authors: Sola F, Canonico B, Montanari M, Volpe A, Barattini C, Pellegrino C, Cesarini E, Guescini M, Battistelli M, Ortolani C, Ventola A, Papa S
Format: Article
Language:English
Published: Dove Medical Press 2021-03-01
Series:Nanotechnology, Science and Applications
Subjects:
Online Access:https://www.dovepress.com/uptake-and-intracellular-trafficking-studies-of-multiple-dye-doped-cor-peer-reviewed-article-NSA
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spelling doaj-79536f0d35b74c6eaee1765589e826a62021-03-09T19:01:43ZengDove Medical PressNanotechnology, Science and Applications1177-89032021-03-01Volume 14294862836Uptake and Intracellular Trafficking Studies of Multiple Dye-Doped Core-Shell Silica Nanoparticles in Lymphoid and Myeloid CellsSola FCanonico BMontanari MVolpe ABarattini CPellegrino CCesarini EGuescini MBattistelli MOrtolani CVentola APapa SFederica Sola,1,2 Barbara Canonico,1 Mariele Montanari,1 Angela Volpe,2 Chiara Barattini,1,2 Chiara Pellegrino,2 Erica Cesarini,1 Michele Guescini,1 Michela Battistelli,1 Claudio Ortolani,1 Alfredo Ventola,2 Stefano Papa1 1Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, PU, 61029, Italy; 2AcZon Srl, Monte San Pietro, BO, 40050, ItalyCorrespondence: Barbara CanonicoDepartment of Biomolecular Sciences, University of Urbino Carlo Bo, Via Ca’ Le Suore 2-4, Urbino, PU, 61029, ItalyTel +39 0722 304280Email barbara.canonico@uniurb.itIntroduction: 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: NTB 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 NTB 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 NTB 700 NPs a promising platform for future development of a multifunctional system, by combining imaging and localized therapeutic applications in a unique tool.Keywords: nanoparticles, uptake, intracellular trafficking, exocytosis, multifunctional toolhttps://www.dovepress.com/uptake-and-intracellular-trafficking-studies-of-multiple-dye-doped-cor-peer-reviewed-article-NSAnanoparticlesuptakeintracellular traffickingexocytosismultifunctional tool
collection DOAJ
language English
format Article
sources DOAJ
author Sola F
Canonico B
Montanari M
Volpe A
Barattini C
Pellegrino C
Cesarini E
Guescini M
Battistelli M
Ortolani C
Ventola A
Papa S
spellingShingle Sola F
Canonico B
Montanari M
Volpe A
Barattini C
Pellegrino C
Cesarini E
Guescini M
Battistelli M
Ortolani C
Ventola A
Papa S
Uptake and Intracellular Trafficking Studies of Multiple Dye-Doped Core-Shell Silica Nanoparticles in Lymphoid and Myeloid Cells
Nanotechnology, Science and Applications
nanoparticles
uptake
intracellular trafficking
exocytosis
multifunctional tool
author_facet Sola F
Canonico B
Montanari M
Volpe A
Barattini C
Pellegrino C
Cesarini E
Guescini M
Battistelli M
Ortolani C
Ventola A
Papa S
author_sort Sola F
title 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_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_sort uptake and intracellular trafficking studies of multiple dye-doped core-shell silica nanoparticles in lymphoid and myeloid cells
publisher Dove Medical Press
series Nanotechnology, Science and Applications
issn 1177-8903
publishDate 2021-03-01
description Federica Sola,1,2 Barbara Canonico,1 Mariele Montanari,1 Angela Volpe,2 Chiara Barattini,1,2 Chiara Pellegrino,2 Erica Cesarini,1 Michele Guescini,1 Michela Battistelli,1 Claudio Ortolani,1 Alfredo Ventola,2 Stefano Papa1 1Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, PU, 61029, Italy; 2AcZon Srl, Monte San Pietro, BO, 40050, ItalyCorrespondence: Barbara CanonicoDepartment of Biomolecular Sciences, University of Urbino Carlo Bo, Via Ca’ Le Suore 2-4, Urbino, PU, 61029, ItalyTel +39 0722 304280Email barbara.canonico@uniurb.itIntroduction: 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: NTB 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 NTB 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 NTB 700 NPs a promising platform for future development of a multifunctional system, by combining imaging and localized therapeutic applications in a unique tool.Keywords: nanoparticles, uptake, intracellular trafficking, exocytosis, multifunctional tool
topic nanoparticles
uptake
intracellular trafficking
exocytosis
multifunctional tool
url https://www.dovepress.com/uptake-and-intracellular-trafficking-studies-of-multiple-dye-doped-cor-peer-reviewed-article-NSA
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