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Self-Assembled Biocompatible Fluorescent Nanoparticles for Bioimaging

Fluorescence is a powerful tool for mapping biological events in real-time with high spatial resolution. Ultra-bright probes are needed in order to achieve high sensitivity: these probes are typically obtained by gathering a huge number of fluorophores in a single nanoparticle (NP). Unfortunately th...

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Autores principales: Caponetti, Valeria, Trzcinski, Jakub W., Cantelli, Andrea, Tavano, Regina, Papini, Emanuele, Mancin, Fabrizio, Montalti, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447614/
https://www.ncbi.nlm.nih.gov/pubmed/30984740
http://dx.doi.org/10.3389/fchem.2019.00168
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author Caponetti, Valeria
Trzcinski, Jakub W.
Cantelli, Andrea
Tavano, Regina
Papini, Emanuele
Mancin, Fabrizio
Montalti, Marco
author_facet Caponetti, Valeria
Trzcinski, Jakub W.
Cantelli, Andrea
Tavano, Regina
Papini, Emanuele
Mancin, Fabrizio
Montalti, Marco
author_sort Caponetti, Valeria
collection PubMed
description Fluorescence is a powerful tool for mapping biological events in real-time with high spatial resolution. Ultra-bright probes are needed in order to achieve high sensitivity: these probes are typically obtained by gathering a huge number of fluorophores in a single nanoparticle (NP). Unfortunately this assembly produces quenching of the fluorescence because of short-range intermolecular interactions. Here we demonstrate that rational structural modification of a well-known molecular fluorophore N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) (NBD) produces fluorophores that self-assemble in nanoparticles in the biocompatible environment without any dramatic decrease of the fluorescence quantum yield. Most importantly, the resulting NP show, in an aqueous environment, a brightness which is more than six orders of magnitude higher than the molecular component in the organic solvent. Moreover, the NP are prepared by nanoprecipitation and they are stabilized only via non-covalent interaction, they are surprisingly stable and can be observed as individual bright spots freely diffusing in solution at a concentration as low as 1 nM. The suitability of the NP as biocompatible fluorescent probes was demonstrated in the case of HeLa cells by fluorescence confocal microscopy and MTS assays.
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spelling pubmed-64476142019-04-12 Self-Assembled Biocompatible Fluorescent Nanoparticles for Bioimaging Caponetti, Valeria Trzcinski, Jakub W. Cantelli, Andrea Tavano, Regina Papini, Emanuele Mancin, Fabrizio Montalti, Marco Front Chem Chemistry Fluorescence is a powerful tool for mapping biological events in real-time with high spatial resolution. Ultra-bright probes are needed in order to achieve high sensitivity: these probes are typically obtained by gathering a huge number of fluorophores in a single nanoparticle (NP). Unfortunately this assembly produces quenching of the fluorescence because of short-range intermolecular interactions. Here we demonstrate that rational structural modification of a well-known molecular fluorophore N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) (NBD) produces fluorophores that self-assemble in nanoparticles in the biocompatible environment without any dramatic decrease of the fluorescence quantum yield. Most importantly, the resulting NP show, in an aqueous environment, a brightness which is more than six orders of magnitude higher than the molecular component in the organic solvent. Moreover, the NP are prepared by nanoprecipitation and they are stabilized only via non-covalent interaction, they are surprisingly stable and can be observed as individual bright spots freely diffusing in solution at a concentration as low as 1 nM. The suitability of the NP as biocompatible fluorescent probes was demonstrated in the case of HeLa cells by fluorescence confocal microscopy and MTS assays. Frontiers Media S.A. 2019-03-28 /pmc/articles/PMC6447614/ /pubmed/30984740 http://dx.doi.org/10.3389/fchem.2019.00168 Text en Copyright © 2019 Caponetti, Trzcinski, Cantelli, Tavano, Papini, Mancin and Montalti. 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
Caponetti, Valeria
Trzcinski, Jakub W.
Cantelli, Andrea
Tavano, Regina
Papini, Emanuele
Mancin, Fabrizio
Montalti, Marco
Self-Assembled Biocompatible Fluorescent Nanoparticles for Bioimaging
title Self-Assembled Biocompatible Fluorescent Nanoparticles for Bioimaging
title_full Self-Assembled Biocompatible Fluorescent Nanoparticles for Bioimaging
title_fullStr Self-Assembled Biocompatible Fluorescent Nanoparticles for Bioimaging
title_full_unstemmed Self-Assembled Biocompatible Fluorescent Nanoparticles for Bioimaging
title_short Self-Assembled Biocompatible Fluorescent Nanoparticles for Bioimaging
title_sort self-assembled biocompatible fluorescent nanoparticles for bioimaging
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447614/
https://www.ncbi.nlm.nih.gov/pubmed/30984740
http://dx.doi.org/10.3389/fchem.2019.00168
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