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Antimicrobial and Antibiofilm Photodynamic Action of Photosensitizing Nanoassemblies Based on Sulfobutylether-β-Cyclodextrin
Developing new broad-spectrum antimicrobial strategies, as alternatives to antibiotics and being able to efficiently inactivate pathogens without inducing resistance, is one of the main objectives in public health. Antimicrobial photodynamic therapy (aPDT), based on the light-induced production of r...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10051317/ https://www.ncbi.nlm.nih.gov/pubmed/36985465 http://dx.doi.org/10.3390/molecules28062493 |
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author | Franco, Domenico Zagami, Roberto De Plano, Laura Maria Burduja, Nina Guglielmino, Salvatore Pietro Paolo Scolaro, Luigi Monsù Mazzaglia, Antonino |
author_facet | Franco, Domenico Zagami, Roberto De Plano, Laura Maria Burduja, Nina Guglielmino, Salvatore Pietro Paolo Scolaro, Luigi Monsù Mazzaglia, Antonino |
author_sort | Franco, Domenico |
collection | PubMed |
description | Developing new broad-spectrum antimicrobial strategies, as alternatives to antibiotics and being able to efficiently inactivate pathogens without inducing resistance, is one of the main objectives in public health. Antimicrobial photodynamic therapy (aPDT), based on the light-induced production of reactive oxygen species from photosensitizers (PS), is attracting growing interest in the context of infection treatment, also including biofilm destruction. Due to the limited photostability of free PS, delivery systems are increasingly needed in order to decrease PS photodegradation, thus improving the therapeutic efficacy, as well as to reduce collateral effects on unaffected tissues. In this study, we propose a photosensitizing nanosystem based on the cationic porphyrin 5,10,15,20-tetrakis (N-methyl- 4-pyridyl)-21H,23H-porphyrin (TMPyP), complexed with the commerical sulfobutylether-beta-cyclodextrin (CAPTISOL(®)), at a 1:50 molar ratio (CAPTISOL(®)/TMPyP)(50_1). Nanoassemblies based on (CAPTISOL(®)/TMPyP)(50_1) with photodynamic features exhibited photo-antimicrobial activity against Gram-negative and Gram-positive bacteria. Moreover, results from P. aeruginosa reveal that CAPTISOL(®) alone inhibits pyocyanin (PYO) production, also affecting bacterial biofilm formation. Finally, we obtained a synergistic effect of inhibition and destruction of P. aeruginosa biofilm by using the combination of CAPTISOL(®) and TMPyP. |
format | Online Article Text |
id | pubmed-10051317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100513172023-03-30 Antimicrobial and Antibiofilm Photodynamic Action of Photosensitizing Nanoassemblies Based on Sulfobutylether-β-Cyclodextrin Franco, Domenico Zagami, Roberto De Plano, Laura Maria Burduja, Nina Guglielmino, Salvatore Pietro Paolo Scolaro, Luigi Monsù Mazzaglia, Antonino Molecules Article Developing new broad-spectrum antimicrobial strategies, as alternatives to antibiotics and being able to efficiently inactivate pathogens without inducing resistance, is one of the main objectives in public health. Antimicrobial photodynamic therapy (aPDT), based on the light-induced production of reactive oxygen species from photosensitizers (PS), is attracting growing interest in the context of infection treatment, also including biofilm destruction. Due to the limited photostability of free PS, delivery systems are increasingly needed in order to decrease PS photodegradation, thus improving the therapeutic efficacy, as well as to reduce collateral effects on unaffected tissues. In this study, we propose a photosensitizing nanosystem based on the cationic porphyrin 5,10,15,20-tetrakis (N-methyl- 4-pyridyl)-21H,23H-porphyrin (TMPyP), complexed with the commerical sulfobutylether-beta-cyclodextrin (CAPTISOL(®)), at a 1:50 molar ratio (CAPTISOL(®)/TMPyP)(50_1). Nanoassemblies based on (CAPTISOL(®)/TMPyP)(50_1) with photodynamic features exhibited photo-antimicrobial activity against Gram-negative and Gram-positive bacteria. Moreover, results from P. aeruginosa reveal that CAPTISOL(®) alone inhibits pyocyanin (PYO) production, also affecting bacterial biofilm formation. Finally, we obtained a synergistic effect of inhibition and destruction of P. aeruginosa biofilm by using the combination of CAPTISOL(®) and TMPyP. MDPI 2023-03-08 /pmc/articles/PMC10051317/ /pubmed/36985465 http://dx.doi.org/10.3390/molecules28062493 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Franco, Domenico Zagami, Roberto De Plano, Laura Maria Burduja, Nina Guglielmino, Salvatore Pietro Paolo Scolaro, Luigi Monsù Mazzaglia, Antonino Antimicrobial and Antibiofilm Photodynamic Action of Photosensitizing Nanoassemblies Based on Sulfobutylether-β-Cyclodextrin |
title | Antimicrobial and Antibiofilm Photodynamic Action of Photosensitizing Nanoassemblies Based on Sulfobutylether-β-Cyclodextrin |
title_full | Antimicrobial and Antibiofilm Photodynamic Action of Photosensitizing Nanoassemblies Based on Sulfobutylether-β-Cyclodextrin |
title_fullStr | Antimicrobial and Antibiofilm Photodynamic Action of Photosensitizing Nanoassemblies Based on Sulfobutylether-β-Cyclodextrin |
title_full_unstemmed | Antimicrobial and Antibiofilm Photodynamic Action of Photosensitizing Nanoassemblies Based on Sulfobutylether-β-Cyclodextrin |
title_short | Antimicrobial and Antibiofilm Photodynamic Action of Photosensitizing Nanoassemblies Based on Sulfobutylether-β-Cyclodextrin |
title_sort | antimicrobial and antibiofilm photodynamic action of photosensitizing nanoassemblies based on sulfobutylether-β-cyclodextrin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10051317/ https://www.ncbi.nlm.nih.gov/pubmed/36985465 http://dx.doi.org/10.3390/molecules28062493 |
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