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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-9078255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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