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Hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogens

In order to develop a technology platform based on two natural compounds from biorenewable resources, a short series of hyaluronan (HA) copolymers grafted with propargylated ferulic acid (HA–FA–Pg) were designed and synthesized to show different grafting degree values and their optical properties we...

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Autores principales: Cappelli, Andrea, Paolino, Marco, Reale, Annalisa, Razzano, Vincenzo, Grisci, Giorgio, Giuliani, Germano, Donati, Alessandro, Bonechi, Claudia, Lamponi, Stefania, Mendichi, Raniero, Battiato, Salvatore, Samperi, Filippo, Makovec, Francesco, Licciardi, Mariano, Depau, Lorenzo, Botta, Chiara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078255/
https://www.ncbi.nlm.nih.gov/pubmed/35539623
http://dx.doi.org/10.1039/c7ra12543g
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author Cappelli, Andrea
Paolino, Marco
Reale, Annalisa
Razzano, Vincenzo
Grisci, Giorgio
Giuliani, Germano
Donati, Alessandro
Bonechi, Claudia
Lamponi, Stefania
Mendichi, Raniero
Battiato, Salvatore
Samperi, Filippo
Makovec, Francesco
Licciardi, Mariano
Depau, Lorenzo
Botta, Chiara
author_facet Cappelli, Andrea
Paolino, Marco
Reale, Annalisa
Razzano, Vincenzo
Grisci, Giorgio
Giuliani, Germano
Donati, Alessandro
Bonechi, Claudia
Lamponi, Stefania
Mendichi, Raniero
Battiato, Salvatore
Samperi, Filippo
Makovec, Francesco
Licciardi, Mariano
Depau, Lorenzo
Botta, Chiara
author_sort Cappelli, Andrea
collection PubMed
description In order to develop a technology platform based on two natural compounds from biorenewable resources, a short series of hyaluronan (HA) copolymers grafted with propargylated ferulic acid (HA–FA–Pg) were designed and synthesized to show different grafting degree values and their optical properties were characterized in comparison with reference compounds containing the same ferulate fluorophore. Interestingly, these studies revealed that the ferulate fluorophore was quite sensitive to the restriction of intramolecular motion and its introduction into the rigid HA backbone, as in HA–FA–Pg graft copolymers, led to higher photoluminescence quantum yield values than those obtained with the isolated fluorophore. Thus, the propargyl groups of HA–FA–Pg derivatives were exploited in the coupling with oleic acid through a biocompatible nona(ethylene glycol) spacer as an example of the possible applications of this technology platform. The resulting HA–FA–NEG–OA materials showed self-assembling capabilities in aqueous environment. Furthermore, HA–FA–NEG–OA derivatives have been shown to interact with phospholipid bilayers both in liposomes and living cells, retaining their fluorogenic properties and showing a high degree of cytocompatibility and for this reason they were proposed as potential biocompatible self-assembled aggregates forming new materials for biomedical applications.
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spelling pubmed-90782552022-05-09 Hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogens Cappelli, Andrea Paolino, Marco Reale, Annalisa Razzano, Vincenzo Grisci, Giorgio Giuliani, Germano Donati, Alessandro Bonechi, Claudia Lamponi, Stefania Mendichi, Raniero Battiato, Salvatore Samperi, Filippo Makovec, Francesco Licciardi, Mariano Depau, Lorenzo Botta, Chiara RSC Adv Chemistry In order to develop a technology platform based on two natural compounds from biorenewable resources, a short series of hyaluronan (HA) copolymers grafted with propargylated ferulic acid (HA–FA–Pg) were designed and synthesized to show different grafting degree values and their optical properties were characterized in comparison with reference compounds containing the same ferulate fluorophore. Interestingly, these studies revealed that the ferulate fluorophore was quite sensitive to the restriction of intramolecular motion and its introduction into the rigid HA backbone, as in HA–FA–Pg graft copolymers, led to higher photoluminescence quantum yield values than those obtained with the isolated fluorophore. Thus, the propargyl groups of HA–FA–Pg derivatives were exploited in the coupling with oleic acid through a biocompatible nona(ethylene glycol) spacer as an example of the possible applications of this technology platform. The resulting HA–FA–NEG–OA materials showed self-assembling capabilities in aqueous environment. Furthermore, HA–FA–NEG–OA derivatives have been shown to interact with phospholipid bilayers both in liposomes and living cells, retaining their fluorogenic properties and showing a high degree of cytocompatibility and for this reason they were proposed as potential biocompatible self-assembled aggregates forming new materials for biomedical applications. The Royal Society of Chemistry 2018-02-06 /pmc/articles/PMC9078255/ /pubmed/35539623 http://dx.doi.org/10.1039/c7ra12543g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Cappelli, Andrea
Paolino, Marco
Reale, Annalisa
Razzano, Vincenzo
Grisci, Giorgio
Giuliani, Germano
Donati, Alessandro
Bonechi, Claudia
Lamponi, Stefania
Mendichi, Raniero
Battiato, Salvatore
Samperi, Filippo
Makovec, Francesco
Licciardi, Mariano
Depau, Lorenzo
Botta, Chiara
Hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogens
title Hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogens
title_full Hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogens
title_fullStr Hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogens
title_full_unstemmed Hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogens
title_short Hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogens
title_sort hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogens
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078255/
https://www.ncbi.nlm.nih.gov/pubmed/35539623
http://dx.doi.org/10.1039/c7ra12543g
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