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Physicochemical Properties of a New PEGylated Polybenzofulvene Brush for Drug Encapsulation

A new polymer brush was synthesized by spontaneous polymerization of benzofulvene macromonomer 6-MOEG-9-T-BF3k bearing a nona(ethylene glycol) side chain linked to the 3-phenylindene scaffold by means of a triazole heterocycle. The polymer structure was studied by SEC-MALS, NMR spectroscopy, and MAL...

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Autores principales: Paolino, Marco, Reale, Annalisa, Razzano, Vincenzo, Giuliani, Germano, Donati, Alessandro, Giorgi, Gianluca, Boccia, Antonella Caterina, Mendichi, Raniero, Piovani, Daniele, Botta, Chiara, Salvini, Laura, Samperi, Filippo, Savoca, Cristina, Licciardi, Mariano, Paccagnini, Eugenio, Gentile, Mariangela, Cappelli, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781277/
https://www.ncbi.nlm.nih.gov/pubmed/31480633
http://dx.doi.org/10.3390/pharmaceutics11090444
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author Paolino, Marco
Reale, Annalisa
Razzano, Vincenzo
Giuliani, Germano
Donati, Alessandro
Giorgi, Gianluca
Boccia, Antonella Caterina
Mendichi, Raniero
Piovani, Daniele
Botta, Chiara
Salvini, Laura
Samperi, Filippo
Savoca, Cristina
Licciardi, Mariano
Paccagnini, Eugenio
Gentile, Mariangela
Cappelli, Andrea
author_facet Paolino, Marco
Reale, Annalisa
Razzano, Vincenzo
Giuliani, Germano
Donati, Alessandro
Giorgi, Gianluca
Boccia, Antonella Caterina
Mendichi, Raniero
Piovani, Daniele
Botta, Chiara
Salvini, Laura
Samperi, Filippo
Savoca, Cristina
Licciardi, Mariano
Paccagnini, Eugenio
Gentile, Mariangela
Cappelli, Andrea
author_sort Paolino, Marco
collection PubMed
description A new polymer brush was synthesized by spontaneous polymerization of benzofulvene macromonomer 6-MOEG-9-T-BF3k bearing a nona(ethylene glycol) side chain linked to the 3-phenylindene scaffold by means of a triazole heterocycle. The polymer structure was studied by SEC-MALS, NMR spectroscopy, and MALDI-TOF MS techniques, and the results supported the role of oligomeric initiatory species in the spontaneous polymerization of polybenzofulvene derivatives. The aggregation features of high molecular weight poly-6-MOEG-9-T-BF3k-FE were investigated by pyrene fluorescence analysis, dynamic light scattering studies, and transmission electron microscopy, which suggested a tendency towards the formation of spherical objects showing dimensions in the range of 20–200 nm. Moreover, poly-6-MOEG-9-T-BF3k-FE showed an interesting cytocompatibility in the whole concentration range tested that, besides its aggregation features, makes this polybenzofulvene brush a good polymer candidate for nanoencapsulation and delivery of drug molecules. Finally, the photo-physical features of poly-6-MOEG-9-T-BF3k-FE could allow the biodistribution of the resulting drug delivery systems to be monitored by fluorescence microscopy techniques.
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spelling pubmed-67812772019-10-30 Physicochemical Properties of a New PEGylated Polybenzofulvene Brush for Drug Encapsulation Paolino, Marco Reale, Annalisa Razzano, Vincenzo Giuliani, Germano Donati, Alessandro Giorgi, Gianluca Boccia, Antonella Caterina Mendichi, Raniero Piovani, Daniele Botta, Chiara Salvini, Laura Samperi, Filippo Savoca, Cristina Licciardi, Mariano Paccagnini, Eugenio Gentile, Mariangela Cappelli, Andrea Pharmaceutics Article A new polymer brush was synthesized by spontaneous polymerization of benzofulvene macromonomer 6-MOEG-9-T-BF3k bearing a nona(ethylene glycol) side chain linked to the 3-phenylindene scaffold by means of a triazole heterocycle. The polymer structure was studied by SEC-MALS, NMR spectroscopy, and MALDI-TOF MS techniques, and the results supported the role of oligomeric initiatory species in the spontaneous polymerization of polybenzofulvene derivatives. The aggregation features of high molecular weight poly-6-MOEG-9-T-BF3k-FE were investigated by pyrene fluorescence analysis, dynamic light scattering studies, and transmission electron microscopy, which suggested a tendency towards the formation of spherical objects showing dimensions in the range of 20–200 nm. Moreover, poly-6-MOEG-9-T-BF3k-FE showed an interesting cytocompatibility in the whole concentration range tested that, besides its aggregation features, makes this polybenzofulvene brush a good polymer candidate for nanoencapsulation and delivery of drug molecules. Finally, the photo-physical features of poly-6-MOEG-9-T-BF3k-FE could allow the biodistribution of the resulting drug delivery systems to be monitored by fluorescence microscopy techniques. MDPI 2019-09-01 /pmc/articles/PMC6781277/ /pubmed/31480633 http://dx.doi.org/10.3390/pharmaceutics11090444 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Paolino, Marco
Reale, Annalisa
Razzano, Vincenzo
Giuliani, Germano
Donati, Alessandro
Giorgi, Gianluca
Boccia, Antonella Caterina
Mendichi, Raniero
Piovani, Daniele
Botta, Chiara
Salvini, Laura
Samperi, Filippo
Savoca, Cristina
Licciardi, Mariano
Paccagnini, Eugenio
Gentile, Mariangela
Cappelli, Andrea
Physicochemical Properties of a New PEGylated Polybenzofulvene Brush for Drug Encapsulation
title Physicochemical Properties of a New PEGylated Polybenzofulvene Brush for Drug Encapsulation
title_full Physicochemical Properties of a New PEGylated Polybenzofulvene Brush for Drug Encapsulation
title_fullStr Physicochemical Properties of a New PEGylated Polybenzofulvene Brush for Drug Encapsulation
title_full_unstemmed Physicochemical Properties of a New PEGylated Polybenzofulvene Brush for Drug Encapsulation
title_short Physicochemical Properties of a New PEGylated Polybenzofulvene Brush for Drug Encapsulation
title_sort physicochemical properties of a new pegylated polybenzofulvene brush for drug encapsulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781277/
https://www.ncbi.nlm.nih.gov/pubmed/31480633
http://dx.doi.org/10.3390/pharmaceutics11090444
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