Ruthenium(II) Polypyridyl Complexes for Antimicrobial Photodynamic Therapy: Prospects for Application in Cystic Fibrosis Lung Airways

Antimicrobial photodynamic therapy (aPDT) depends on a variety of parameters notably related to the photosensitizers used, the pathogens to target and the environment to operate. In a previous study using a series of Ruthenium(II) polypyridyl ([Ru(II)]) complexes, we reported the importance of the c...

Full description

Bibliographic Details
Main Authors: Raphaëlle Youf, Adeel Nasir, Mareike Müller, Franck Thétiot, Tanguy Haute, Rosy Ghanem, Ulrich Jonas, Holger Schönherr, Gilles Lemercier, Tristan Montier, Tony Le Gall
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/14/8/1664
_version_ 1827617635774234624
author Raphaëlle Youf
Adeel Nasir
Mareike Müller
Franck Thétiot
Tanguy Haute
Rosy Ghanem
Ulrich Jonas
Holger Schönherr
Gilles Lemercier
Tristan Montier
Tony Le Gall
author_facet Raphaëlle Youf
Adeel Nasir
Mareike Müller
Franck Thétiot
Tanguy Haute
Rosy Ghanem
Ulrich Jonas
Holger Schönherr
Gilles Lemercier
Tristan Montier
Tony Le Gall
author_sort Raphaëlle Youf
collection DOAJ
description Antimicrobial photodynamic therapy (aPDT) depends on a variety of parameters notably related to the photosensitizers used, the pathogens to target and the environment to operate. In a previous study using a series of Ruthenium(II) polypyridyl ([Ru(II)]) complexes, we reported the importance of the chemical structure on both their photo-physical/physico-chemical properties and their efficacy for aPDT. By employing standard in vitro conditions, effective [Ru(II)]-mediated aPDT was demonstrated against planktonic cultures of <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i> strains notably isolated from the airways of Cystic Fibrosis (CF) patients. CF lung disease is characterized with many pathophysiological disorders that can compromise the effectiveness of antimicrobials. Taking this into account, the present study is an extension of our previous work, with the aim of further investigating [Ru(II)]-mediated aPDT under in vitro experimental settings approaching the conditions of infected airways in CF patients. Thus, we herein studied the isolated influence of a series of parameters (including increased osmotic strength, acidic pH, lower oxygen availability, artificial sputum medium and biofilm formation) on the properties of two selected [Ru(II)] complexes. Furthermore, these compounds were used to evaluate the possibility to photoinactivate <i>P. aeruginosa</i> while preserving an underlying epithelium of human bronchial epithelial cells. Altogether, our results provide substantial evidence for the relevance of [Ru(II)]-based aPDT in CF lung airways. Besides optimized nano-complexes, this study also highlights the various needs for translating such a challenging perspective into clinical practice.
first_indexed 2024-03-09T09:50:50Z
format Article
id doaj.art-4ae796bf5835497f8b116f507c6f3135
institution Directory Open Access Journal
issn 1999-4923
language English
last_indexed 2024-03-09T09:50:50Z
publishDate 2022-08-01
publisher MDPI AG
record_format Article
series Pharmaceutics
spelling doaj.art-4ae796bf5835497f8b116f507c6f31352023-12-02T00:10:00ZengMDPI AGPharmaceutics1999-49232022-08-01148166410.3390/pharmaceutics14081664Ruthenium(II) Polypyridyl Complexes for Antimicrobial Photodynamic Therapy: Prospects for Application in Cystic Fibrosis Lung AirwaysRaphaëlle Youf0Adeel Nasir1Mareike Müller2Franck Thétiot3Tanguy Haute4Rosy Ghanem5Ulrich Jonas6Holger Schönherr7Gilles Lemercier8Tristan Montier9Tony Le Gall10INSERM, Univ Brest, EFS, UMR 1078, GGB-GTCA, 29200 Brest, FranceINSERM, Univ Brest, EFS, UMR 1078, GGB-GTCA, 29200 Brest, FrancePhysical Chemistry I & Research Center of Micro- and Nanochemistry and (Bio)Technology (Cμ), Department of Chemistry and Biology, University of Siegen, 57076 Siegen, GermanyUnité Mixte de Recherche (UMR), Centre National de la Recherche Scientifique (CNRS) 6521, Université de Brest (UBO), CS 93837, 29238 Brest, FranceINSERM, Univ Brest, EFS, UMR 1078, GGB-GTCA, 29200 Brest, FranceINSERM, Univ Brest, EFS, UMR 1078, GGB-GTCA, 29200 Brest, FranceMacromolecular Chemistry, Department of Chemistry and Biology, University of Siegen, 57076 Siegen, GermanyPhysical Chemistry I & Research Center of Micro- and Nanochemistry and (Bio)Technology (Cμ), Department of Chemistry and Biology, University of Siegen, 57076 Siegen, GermanyCoordination Chemistry Team, Unité Mixte de Recherche (UMR), Centre National de la Recherche Scientifique (CNRS) 7312, Institut de Chimie Moléculaire de Reims (ICMR), Université de Reims Champagne-Ardenne, BP 1039, CEDEX 2, 51687 Reims, FranceINSERM, Univ Brest, EFS, UMR 1078, GGB-GTCA, 29200 Brest, FranceINSERM, Univ Brest, EFS, UMR 1078, GGB-GTCA, 29200 Brest, FranceAntimicrobial photodynamic therapy (aPDT) depends on a variety of parameters notably related to the photosensitizers used, the pathogens to target and the environment to operate. In a previous study using a series of Ruthenium(II) polypyridyl ([Ru(II)]) complexes, we reported the importance of the chemical structure on both their photo-physical/physico-chemical properties and their efficacy for aPDT. By employing standard in vitro conditions, effective [Ru(II)]-mediated aPDT was demonstrated against planktonic cultures of <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i> strains notably isolated from the airways of Cystic Fibrosis (CF) patients. CF lung disease is characterized with many pathophysiological disorders that can compromise the effectiveness of antimicrobials. Taking this into account, the present study is an extension of our previous work, with the aim of further investigating [Ru(II)]-mediated aPDT under in vitro experimental settings approaching the conditions of infected airways in CF patients. Thus, we herein studied the isolated influence of a series of parameters (including increased osmotic strength, acidic pH, lower oxygen availability, artificial sputum medium and biofilm formation) on the properties of two selected [Ru(II)] complexes. Furthermore, these compounds were used to evaluate the possibility to photoinactivate <i>P. aeruginosa</i> while preserving an underlying epithelium of human bronchial epithelial cells. Altogether, our results provide substantial evidence for the relevance of [Ru(II)]-based aPDT in CF lung airways. Besides optimized nano-complexes, this study also highlights the various needs for translating such a challenging perspective into clinical practice.https://www.mdpi.com/1999-4923/14/8/1664antimicrobial photodynamic therapyantimicrobial resistancebiofilmbenchmark analysiscystic fibrosismicro-environment
spellingShingle Raphaëlle Youf
Adeel Nasir
Mareike Müller
Franck Thétiot
Tanguy Haute
Rosy Ghanem
Ulrich Jonas
Holger Schönherr
Gilles Lemercier
Tristan Montier
Tony Le Gall
Ruthenium(II) Polypyridyl Complexes for Antimicrobial Photodynamic Therapy: Prospects for Application in Cystic Fibrosis Lung Airways
Pharmaceutics
antimicrobial photodynamic therapy
antimicrobial resistance
biofilm
benchmark analysis
cystic fibrosis
micro-environment
title Ruthenium(II) Polypyridyl Complexes for Antimicrobial Photodynamic Therapy: Prospects for Application in Cystic Fibrosis Lung Airways
title_full Ruthenium(II) Polypyridyl Complexes for Antimicrobial Photodynamic Therapy: Prospects for Application in Cystic Fibrosis Lung Airways
title_fullStr Ruthenium(II) Polypyridyl Complexes for Antimicrobial Photodynamic Therapy: Prospects for Application in Cystic Fibrosis Lung Airways
title_full_unstemmed Ruthenium(II) Polypyridyl Complexes for Antimicrobial Photodynamic Therapy: Prospects for Application in Cystic Fibrosis Lung Airways
title_short Ruthenium(II) Polypyridyl Complexes for Antimicrobial Photodynamic Therapy: Prospects for Application in Cystic Fibrosis Lung Airways
title_sort ruthenium ii polypyridyl complexes for antimicrobial photodynamic therapy prospects for application in cystic fibrosis lung airways
topic antimicrobial photodynamic therapy
antimicrobial resistance
biofilm
benchmark analysis
cystic fibrosis
micro-environment
url https://www.mdpi.com/1999-4923/14/8/1664
work_keys_str_mv AT raphaelleyouf rutheniumiipolypyridylcomplexesforantimicrobialphotodynamictherapyprospectsforapplicationincysticfibrosislungairways
AT adeelnasir rutheniumiipolypyridylcomplexesforantimicrobialphotodynamictherapyprospectsforapplicationincysticfibrosislungairways
AT mareikemuller rutheniumiipolypyridylcomplexesforantimicrobialphotodynamictherapyprospectsforapplicationincysticfibrosislungairways
AT franckthetiot rutheniumiipolypyridylcomplexesforantimicrobialphotodynamictherapyprospectsforapplicationincysticfibrosislungairways
AT tanguyhaute rutheniumiipolypyridylcomplexesforantimicrobialphotodynamictherapyprospectsforapplicationincysticfibrosislungairways
AT rosyghanem rutheniumiipolypyridylcomplexesforantimicrobialphotodynamictherapyprospectsforapplicationincysticfibrosislungairways
AT ulrichjonas rutheniumiipolypyridylcomplexesforantimicrobialphotodynamictherapyprospectsforapplicationincysticfibrosislungairways
AT holgerschonherr rutheniumiipolypyridylcomplexesforantimicrobialphotodynamictherapyprospectsforapplicationincysticfibrosislungairways
AT gilleslemercier rutheniumiipolypyridylcomplexesforantimicrobialphotodynamictherapyprospectsforapplicationincysticfibrosislungairways
AT tristanmontier rutheniumiipolypyridylcomplexesforantimicrobialphotodynamictherapyprospectsforapplicationincysticfibrosislungairways
AT tonylegall rutheniumiipolypyridylcomplexesforantimicrobialphotodynamictherapyprospectsforapplicationincysticfibrosislungairways