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The B & B approach: Ball-milling conjugation of dextran with phenylboronic acid (PBA)-functionalized BODIPY
Mechanochemistry is an emerging and reliable alternative to conventional solution (batch) synthesis of complex molecules under green and solvent-free conditions. In this regard, we report here on the conjugation of a dextran polysaccharide with a fluorescent probe, a phenylboronic acid (PBA)-functio...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492696/ https://www.ncbi.nlm.nih.gov/pubmed/32983271 http://dx.doi.org/10.3762/bjoc.16.188 |
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author | Andreozzi, Patrizia Tamberi, Lorenza Tasca, Elisamaria Giacomazzo, Gina Elena Martinez, Marta Severi, Mirko Marradi, Marco Cicchi, Stefano Moya, Sergio Biagiotti, Giacomo Richichi, Barbara |
author_facet | Andreozzi, Patrizia Tamberi, Lorenza Tasca, Elisamaria Giacomazzo, Gina Elena Martinez, Marta Severi, Mirko Marradi, Marco Cicchi, Stefano Moya, Sergio Biagiotti, Giacomo Richichi, Barbara |
author_sort | Andreozzi, Patrizia |
collection | PubMed |
description | Mechanochemistry is an emerging and reliable alternative to conventional solution (batch) synthesis of complex molecules under green and solvent-free conditions. In this regard, we report here on the conjugation of a dextran polysaccharide with a fluorescent probe, a phenylboronic acid (PBA)-functionalized boron dipyrromethene (BODIPY) applying the ball milling approach. The ball milling formation of boron esters between PBA BODIPY and dextran proved to be more efficient in terms of reaction time, amount of reactants, and labelling degree compared to the corresponding solution-based synthetic route. PBA-BODIPY dextran assembles into nanoparticles of around 200 nm by hydrophobic interactions. The resulting PBA-BODIPY dextran nanoparticles retain an apolar interior as proved by pyrene fluorescence, suitable for the encapsulation of hydrophobic drugs with high biocompatibility while remaining fluorescent. |
format | Online Article Text |
id | pubmed-7492696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-74926962020-09-24 The B & B approach: Ball-milling conjugation of dextran with phenylboronic acid (PBA)-functionalized BODIPY Andreozzi, Patrizia Tamberi, Lorenza Tasca, Elisamaria Giacomazzo, Gina Elena Martinez, Marta Severi, Mirko Marradi, Marco Cicchi, Stefano Moya, Sergio Biagiotti, Giacomo Richichi, Barbara Beilstein J Org Chem Full Research Paper Mechanochemistry is an emerging and reliable alternative to conventional solution (batch) synthesis of complex molecules under green and solvent-free conditions. In this regard, we report here on the conjugation of a dextran polysaccharide with a fluorescent probe, a phenylboronic acid (PBA)-functionalized boron dipyrromethene (BODIPY) applying the ball milling approach. The ball milling formation of boron esters between PBA BODIPY and dextran proved to be more efficient in terms of reaction time, amount of reactants, and labelling degree compared to the corresponding solution-based synthetic route. PBA-BODIPY dextran assembles into nanoparticles of around 200 nm by hydrophobic interactions. The resulting PBA-BODIPY dextran nanoparticles retain an apolar interior as proved by pyrene fluorescence, suitable for the encapsulation of hydrophobic drugs with high biocompatibility while remaining fluorescent. Beilstein-Institut 2020-09-11 /pmc/articles/PMC7492696/ /pubmed/32983271 http://dx.doi.org/10.3762/bjoc.16.188 Text en Copyright © 2020, Andreozzi et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Andreozzi, Patrizia Tamberi, Lorenza Tasca, Elisamaria Giacomazzo, Gina Elena Martinez, Marta Severi, Mirko Marradi, Marco Cicchi, Stefano Moya, Sergio Biagiotti, Giacomo Richichi, Barbara The B & B approach: Ball-milling conjugation of dextran with phenylboronic acid (PBA)-functionalized BODIPY |
title | The B & B approach: Ball-milling conjugation of dextran with phenylboronic acid (PBA)-functionalized BODIPY |
title_full | The B & B approach: Ball-milling conjugation of dextran with phenylboronic acid (PBA)-functionalized BODIPY |
title_fullStr | The B & B approach: Ball-milling conjugation of dextran with phenylboronic acid (PBA)-functionalized BODIPY |
title_full_unstemmed | The B & B approach: Ball-milling conjugation of dextran with phenylboronic acid (PBA)-functionalized BODIPY |
title_short | The B & B approach: Ball-milling conjugation of dextran with phenylboronic acid (PBA)-functionalized BODIPY |
title_sort | b & b approach: ball-milling conjugation of dextran with phenylboronic acid (pba)-functionalized bodipy |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492696/ https://www.ncbi.nlm.nih.gov/pubmed/32983271 http://dx.doi.org/10.3762/bjoc.16.188 |
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