Role of Polymer Micelles in the Delivery of Photodynamic Therapy Agent to Liposomes and Cells

The use of nanocarriers for hydrophobic photosensitizers, in the context of photodynamic therapy (PDT) to improve pharmacokinetics and bio-distribution, is well-established. However, the mechanisms at play in the internalization of nanocarriers are not well-elucidated, despite its importance in nano...

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Main Authors: Laure Gibot, Maxime Demazeau, Véronique Pimienta, Anne-Françoise Mingotaud, Patricia Vicendo, Fabrice Collin, Nathalie Martins-Froment, Stéphane Dejean, Benjamin Nottelet, Clément Roux, Barbara Lonetti
Format: Article
Language:English
Published: MDPI AG 2020-02-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/12/2/384
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spelling doaj-f9a670d76d164f6a8a149c5de6ace2ff2020-11-25T02:03:34ZengMDPI AGCancers2072-66942020-02-0112238410.3390/cancers12020384cancers12020384Role of Polymer Micelles in the Delivery of Photodynamic Therapy Agent to Liposomes and CellsLaure Gibot0Maxime Demazeau1Véronique Pimienta2Anne-Françoise Mingotaud3Patricia Vicendo4Fabrice Collin5Nathalie Martins-Froment6Stéphane Dejean7Benjamin Nottelet8Clément Roux9Barbara Lonetti10Laboratoire des IMRCP, Université de Toulouse, CNRS UMR 5623, Université Toulouse III—Paul Sabatier, F-31062 Toulouse, FranceLaboratoire des IMRCP, Université de Toulouse, CNRS UMR 5623, Université Toulouse III—Paul Sabatier, F-31062 Toulouse, FranceLaboratoire des IMRCP, Université de Toulouse, CNRS UMR 5623, Université Toulouse III—Paul Sabatier, F-31062 Toulouse, FranceLaboratoire des IMRCP, Université de Toulouse, CNRS UMR 5623, Université Toulouse III—Paul Sabatier, F-31062 Toulouse, FranceLaboratoire des IMRCP, Université de Toulouse, CNRS UMR 5623, Université Toulouse III—Paul Sabatier, F-31062 Toulouse, FranceLaboratoire des IMRCP, Université de Toulouse, CNRS UMR 5623, Université Toulouse III—Paul Sabatier, F-31062 Toulouse, FranceService Commun de Spectrométrie de Masse (FR2599), Université de Toulouse III (Paul Sabatier), 118, route de Narbonne, F-31062 Toulouse Cedex 9, FranceIBMM, Université de Montpellier, CNRS, ENSCM, 34 090 Montpellier, FranceIBMM, Université de Montpellier, CNRS, ENSCM, 34 090 Montpellier, FranceLaboratoire des IMRCP, Université de Toulouse, CNRS UMR 5623, Université Toulouse III—Paul Sabatier, F-31062 Toulouse, FranceLaboratoire des IMRCP, Université de Toulouse, CNRS UMR 5623, Université Toulouse III—Paul Sabatier, F-31062 Toulouse, FranceThe use of nanocarriers for hydrophobic photosensitizers, in the context of photodynamic therapy (PDT) to improve pharmacokinetics and bio-distribution, is well-established. However, the mechanisms at play in the internalization of nanocarriers are not well-elucidated, despite its importance in nanocarrier design. In this study, we focus on the mechanisms involved in copolymer poly(ethylene oxide)-<i>block</i>-poly(&#949;-caprolactone) PEO-PCL and poly(ethylene oxide)-<i>block</i>-poly styrene PEO-PS micelles - membrane interactions through complementary physico-chemical studies on biomimetic membranes, and biological experiments on two-dimensional (2D) and three-dimensional (3D) cell cultures. F&#246;rster Resonance Energy Transfer measurements on fluorescently-labelled lipid vesicles, and flow cytometry on two cancerous cell lines enabled the evaluation in the uptake of a photosensitizer, Pheophorbide <i>a</i> (Pheo), and copolymer chains towards model membranes, and cells, respectively. The effects of calibrated light illumination for PDT treatment on lipid vesicle membranes, i.e., leakage and formation of oxidized lipids, and cell viability, were assessed. No significant differences were observed between the ability of PEO-PCL and PEO-PS micelles in delivering Pheo to model membranes, but Pheo was found in higher concentrations in cells in the case of PEO-PCL. These higher Pheo concentrations did not correspond to better performances in PDT treatment. We demonstrated that there are subtle differences in PEO-PCL and PEO-PS micelles for the delivery of Pheo.https://www.mdpi.com/2072-6694/12/2/384photodynamic therapyself-assemblypolymerpeo-pclpeo-psmodel membranes
collection DOAJ
language English
format Article
sources DOAJ
author Laure Gibot
Maxime Demazeau
Véronique Pimienta
Anne-Françoise Mingotaud
Patricia Vicendo
Fabrice Collin
Nathalie Martins-Froment
Stéphane Dejean
Benjamin Nottelet
Clément Roux
Barbara Lonetti
spellingShingle Laure Gibot
Maxime Demazeau
Véronique Pimienta
Anne-Françoise Mingotaud
Patricia Vicendo
Fabrice Collin
Nathalie Martins-Froment
Stéphane Dejean
Benjamin Nottelet
Clément Roux
Barbara Lonetti
Role of Polymer Micelles in the Delivery of Photodynamic Therapy Agent to Liposomes and Cells
Cancers
photodynamic therapy
self-assembly
polymer
peo-pcl
peo-ps
model membranes
author_facet Laure Gibot
Maxime Demazeau
Véronique Pimienta
Anne-Françoise Mingotaud
Patricia Vicendo
Fabrice Collin
Nathalie Martins-Froment
Stéphane Dejean
Benjamin Nottelet
Clément Roux
Barbara Lonetti
author_sort Laure Gibot
title Role of Polymer Micelles in the Delivery of Photodynamic Therapy Agent to Liposomes and Cells
title_short Role of Polymer Micelles in the Delivery of Photodynamic Therapy Agent to Liposomes and Cells
title_full Role of Polymer Micelles in the Delivery of Photodynamic Therapy Agent to Liposomes and Cells
title_fullStr Role of Polymer Micelles in the Delivery of Photodynamic Therapy Agent to Liposomes and Cells
title_full_unstemmed Role of Polymer Micelles in the Delivery of Photodynamic Therapy Agent to Liposomes and Cells
title_sort role of polymer micelles in the delivery of photodynamic therapy agent to liposomes and cells
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2020-02-01
description The use of nanocarriers for hydrophobic photosensitizers, in the context of photodynamic therapy (PDT) to improve pharmacokinetics and bio-distribution, is well-established. However, the mechanisms at play in the internalization of nanocarriers are not well-elucidated, despite its importance in nanocarrier design. In this study, we focus on the mechanisms involved in copolymer poly(ethylene oxide)-<i>block</i>-poly(&#949;-caprolactone) PEO-PCL and poly(ethylene oxide)-<i>block</i>-poly styrene PEO-PS micelles - membrane interactions through complementary physico-chemical studies on biomimetic membranes, and biological experiments on two-dimensional (2D) and three-dimensional (3D) cell cultures. F&#246;rster Resonance Energy Transfer measurements on fluorescently-labelled lipid vesicles, and flow cytometry on two cancerous cell lines enabled the evaluation in the uptake of a photosensitizer, Pheophorbide <i>a</i> (Pheo), and copolymer chains towards model membranes, and cells, respectively. The effects of calibrated light illumination for PDT treatment on lipid vesicle membranes, i.e., leakage and formation of oxidized lipids, and cell viability, were assessed. No significant differences were observed between the ability of PEO-PCL and PEO-PS micelles in delivering Pheo to model membranes, but Pheo was found in higher concentrations in cells in the case of PEO-PCL. These higher Pheo concentrations did not correspond to better performances in PDT treatment. We demonstrated that there are subtle differences in PEO-PCL and PEO-PS micelles for the delivery of Pheo.
topic photodynamic therapy
self-assembly
polymer
peo-pcl
peo-ps
model membranes
url https://www.mdpi.com/2072-6694/12/2/384
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