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Polythiophenes with Cationic Phosphonium Groups as Vectors for Imaging, siRNA Delivery, and Photodynamic Therapy

In this work, we exploit the versatile function of cationic phosphonium-conjugated polythiophenes to develop multifunctional platforms for imaging and combined therapy (siRNA delivery and photodynamic therapy). The photophysical properties (absorption, emission and light-induced generation of single...

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Autores principales: Lichon, Laure, Kotras, Clément, Myrzakhmetov, Bauyrzhan, Arnoux, Philippe, Daurat, Morgane, Nguyen, Christophe, Durand, Denis, Bouchmella, Karim, Ali, Lamiaa Mohamed Ahmed, Durand, Jean-Olivier, Richeter, Sébastien, Frochot, Céline, Gary-Bobo, Magali, Surin, Mathieu, Clément, Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466636/
https://www.ncbi.nlm.nih.gov/pubmed/32708042
http://dx.doi.org/10.3390/nano10081432
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author Lichon, Laure
Kotras, Clément
Myrzakhmetov, Bauyrzhan
Arnoux, Philippe
Daurat, Morgane
Nguyen, Christophe
Durand, Denis
Bouchmella, Karim
Ali, Lamiaa Mohamed Ahmed
Durand, Jean-Olivier
Richeter, Sébastien
Frochot, Céline
Gary-Bobo, Magali
Surin, Mathieu
Clément, Sébastien
author_facet Lichon, Laure
Kotras, Clément
Myrzakhmetov, Bauyrzhan
Arnoux, Philippe
Daurat, Morgane
Nguyen, Christophe
Durand, Denis
Bouchmella, Karim
Ali, Lamiaa Mohamed Ahmed
Durand, Jean-Olivier
Richeter, Sébastien
Frochot, Céline
Gary-Bobo, Magali
Surin, Mathieu
Clément, Sébastien
author_sort Lichon, Laure
collection PubMed
description In this work, we exploit the versatile function of cationic phosphonium-conjugated polythiophenes to develop multifunctional platforms for imaging and combined therapy (siRNA delivery and photodynamic therapy). The photophysical properties (absorption, emission and light-induced generation of singlet oxygen) of these cationic polythiophenes were found to be sensitive to molecular weight. Upon light irradiation, low molecular weight cationic polythiophenes were able to light-sensitize surrounding oxygen into reactive oxygen species (ROS) while the highest were not due to its aggregation in aqueous media. These polymers are also fluorescent, allowing one to visualize their intracellular location through confocal microscopy. The most promising polymers were then used as vectors for siRNA delivery. Due to their cationic and amphipathic features, these polymers were found to effectively self-assemble with siRNA targeting the luciferase gene and deliver it in MDA-MB-231 cancer cells expressing luciferase, leading to 30–50% of the gene-silencing effect. In parallel, the photodynamic therapy (PDT) activity of these cationic polymers was restored after siRNA delivery, demonstrating their potential for combined PDT and gene therapy.
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spelling pubmed-74666362020-09-14 Polythiophenes with Cationic Phosphonium Groups as Vectors for Imaging, siRNA Delivery, and Photodynamic Therapy Lichon, Laure Kotras, Clément Myrzakhmetov, Bauyrzhan Arnoux, Philippe Daurat, Morgane Nguyen, Christophe Durand, Denis Bouchmella, Karim Ali, Lamiaa Mohamed Ahmed Durand, Jean-Olivier Richeter, Sébastien Frochot, Céline Gary-Bobo, Magali Surin, Mathieu Clément, Sébastien Nanomaterials (Basel) Article In this work, we exploit the versatile function of cationic phosphonium-conjugated polythiophenes to develop multifunctional platforms for imaging and combined therapy (siRNA delivery and photodynamic therapy). The photophysical properties (absorption, emission and light-induced generation of singlet oxygen) of these cationic polythiophenes were found to be sensitive to molecular weight. Upon light irradiation, low molecular weight cationic polythiophenes were able to light-sensitize surrounding oxygen into reactive oxygen species (ROS) while the highest were not due to its aggregation in aqueous media. These polymers are also fluorescent, allowing one to visualize their intracellular location through confocal microscopy. The most promising polymers were then used as vectors for siRNA delivery. Due to their cationic and amphipathic features, these polymers were found to effectively self-assemble with siRNA targeting the luciferase gene and deliver it in MDA-MB-231 cancer cells expressing luciferase, leading to 30–50% of the gene-silencing effect. In parallel, the photodynamic therapy (PDT) activity of these cationic polymers was restored after siRNA delivery, demonstrating their potential for combined PDT and gene therapy. MDPI 2020-07-22 /pmc/articles/PMC7466636/ /pubmed/32708042 http://dx.doi.org/10.3390/nano10081432 Text en © 2020 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
Lichon, Laure
Kotras, Clément
Myrzakhmetov, Bauyrzhan
Arnoux, Philippe
Daurat, Morgane
Nguyen, Christophe
Durand, Denis
Bouchmella, Karim
Ali, Lamiaa Mohamed Ahmed
Durand, Jean-Olivier
Richeter, Sébastien
Frochot, Céline
Gary-Bobo, Magali
Surin, Mathieu
Clément, Sébastien
Polythiophenes with Cationic Phosphonium Groups as Vectors for Imaging, siRNA Delivery, and Photodynamic Therapy
title Polythiophenes with Cationic Phosphonium Groups as Vectors for Imaging, siRNA Delivery, and Photodynamic Therapy
title_full Polythiophenes with Cationic Phosphonium Groups as Vectors for Imaging, siRNA Delivery, and Photodynamic Therapy
title_fullStr Polythiophenes with Cationic Phosphonium Groups as Vectors for Imaging, siRNA Delivery, and Photodynamic Therapy
title_full_unstemmed Polythiophenes with Cationic Phosphonium Groups as Vectors for Imaging, siRNA Delivery, and Photodynamic Therapy
title_short Polythiophenes with Cationic Phosphonium Groups as Vectors for Imaging, siRNA Delivery, and Photodynamic Therapy
title_sort polythiophenes with cationic phosphonium groups as vectors for imaging, sirna delivery, and photodynamic therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466636/
https://www.ncbi.nlm.nih.gov/pubmed/32708042
http://dx.doi.org/10.3390/nano10081432
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