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Ruthenium(II) Polypyridyl Complexes and Metronidazole Derivatives: A Powerful Combination in the Design of Photoresponsive Antibacterial Agents Effective under Hypoxic Conditions
[Image: see text] Ruthenium(II) polypyridyl complexes (RPCs) are gaining momentum in photoactivated chemotherapy (PACT), thanks to the possibility of overcoming the classical reliance on molecular oxygen of photodynamic therapy while preserving the selective drug activation by using light. However,...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207323/ https://www.ncbi.nlm.nih.gov/pubmed/37163381 http://dx.doi.org/10.1021/acs.inorgchem.3c00214 |
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author | Giacomazzo, Gina Elena Conti, Luca Fagorzi, Camilla Pagliai, Marco Andreini, Claudia Guerri, Annalisa Perito, Brunella Mengoni, Alessio Valtancoli, Barbara Giorgi, Claudia |
author_facet | Giacomazzo, Gina Elena Conti, Luca Fagorzi, Camilla Pagliai, Marco Andreini, Claudia Guerri, Annalisa Perito, Brunella Mengoni, Alessio Valtancoli, Barbara Giorgi, Claudia |
author_sort | Giacomazzo, Gina Elena |
collection | PubMed |
description | [Image: see text] Ruthenium(II) polypyridyl complexes (RPCs) are gaining momentum in photoactivated chemotherapy (PACT), thanks to the possibility of overcoming the classical reliance on molecular oxygen of photodynamic therapy while preserving the selective drug activation by using light. However, notwithstanding the intriguing perspectives, the translation of such an approach in the development of new antimicrobials has been only barely considered. Herein, MTZH-1 and MTZH-2, two novel analogues of metronidazole (MTZ), a mainstay drug in the treatment of anaerobic bacterial infections, were designed and inserted in the strained ruthenium complexes [Ru(tpy)(dmp)(MTZ-1)]PF(6) (Ru2) and [Ru(tpy)(dmp)(MTZ-2)]PF(6) (Ru3) (tpy = terpyridine, dmp = 2,9-dimethyl-1,10-phenanthroline) (Chart 1). Analogously to the parental compound [Ru(tpy)(dmp)(5NIM)]PF(6) (Ru1) (5-nitroimidazolate), the Ru(II)-imidazolate coordination of MTZ derivatives resulted in promising Ru(II) photocages, capable to easily unleash the bioactive ligands upon light irradiation and increase the antibacterial activity against Bacillus subtilis, which was chosen as a model of Gram-positive bacteria. The photoreleased 5-nitroimidazole-based ligands led to remarkable phototoxicities under hypoxic conditions (<1% O(2)), with the lead compound Ru3 that exhibited the highest potency across the series, being comparable to the one of the clinical drug MTZ. Besides, the chemical architectures of MTZ derivatives made their interaction with NimAunfavorable, being NimA a model of reductases responsible for bacterial resistance against 5-nitroimidazole-based antibiotics, thus hinting at their possible use to combat antimicrobial resistance. This work may therefore provide fundamental knowledge in the design of novel photoresponsive tools to be used in the fight against infectious diseases. For the first time, the effectiveness of the “photorelease antimicrobial therapy” under therapeutically relevant hypoxic conditions was demonstrated. |
format | Online Article Text |
id | pubmed-10207323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102073232023-05-25 Ruthenium(II) Polypyridyl Complexes and Metronidazole Derivatives: A Powerful Combination in the Design of Photoresponsive Antibacterial Agents Effective under Hypoxic Conditions Giacomazzo, Gina Elena Conti, Luca Fagorzi, Camilla Pagliai, Marco Andreini, Claudia Guerri, Annalisa Perito, Brunella Mengoni, Alessio Valtancoli, Barbara Giorgi, Claudia Inorg Chem [Image: see text] Ruthenium(II) polypyridyl complexes (RPCs) are gaining momentum in photoactivated chemotherapy (PACT), thanks to the possibility of overcoming the classical reliance on molecular oxygen of photodynamic therapy while preserving the selective drug activation by using light. However, notwithstanding the intriguing perspectives, the translation of such an approach in the development of new antimicrobials has been only barely considered. Herein, MTZH-1 and MTZH-2, two novel analogues of metronidazole (MTZ), a mainstay drug in the treatment of anaerobic bacterial infections, were designed and inserted in the strained ruthenium complexes [Ru(tpy)(dmp)(MTZ-1)]PF(6) (Ru2) and [Ru(tpy)(dmp)(MTZ-2)]PF(6) (Ru3) (tpy = terpyridine, dmp = 2,9-dimethyl-1,10-phenanthroline) (Chart 1). Analogously to the parental compound [Ru(tpy)(dmp)(5NIM)]PF(6) (Ru1) (5-nitroimidazolate), the Ru(II)-imidazolate coordination of MTZ derivatives resulted in promising Ru(II) photocages, capable to easily unleash the bioactive ligands upon light irradiation and increase the antibacterial activity against Bacillus subtilis, which was chosen as a model of Gram-positive bacteria. The photoreleased 5-nitroimidazole-based ligands led to remarkable phototoxicities under hypoxic conditions (<1% O(2)), with the lead compound Ru3 that exhibited the highest potency across the series, being comparable to the one of the clinical drug MTZ. Besides, the chemical architectures of MTZ derivatives made their interaction with NimAunfavorable, being NimA a model of reductases responsible for bacterial resistance against 5-nitroimidazole-based antibiotics, thus hinting at their possible use to combat antimicrobial resistance. This work may therefore provide fundamental knowledge in the design of novel photoresponsive tools to be used in the fight against infectious diseases. For the first time, the effectiveness of the “photorelease antimicrobial therapy” under therapeutically relevant hypoxic conditions was demonstrated. American Chemical Society 2023-05-10 /pmc/articles/PMC10207323/ /pubmed/37163381 http://dx.doi.org/10.1021/acs.inorgchem.3c00214 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Giacomazzo, Gina Elena Conti, Luca Fagorzi, Camilla Pagliai, Marco Andreini, Claudia Guerri, Annalisa Perito, Brunella Mengoni, Alessio Valtancoli, Barbara Giorgi, Claudia Ruthenium(II) Polypyridyl Complexes and Metronidazole Derivatives: A Powerful Combination in the Design of Photoresponsive Antibacterial Agents Effective under Hypoxic Conditions |
title | Ruthenium(II)
Polypyridyl Complexes and Metronidazole
Derivatives: A Powerful Combination in the Design of Photoresponsive
Antibacterial Agents Effective under Hypoxic Conditions |
title_full | Ruthenium(II)
Polypyridyl Complexes and Metronidazole
Derivatives: A Powerful Combination in the Design of Photoresponsive
Antibacterial Agents Effective under Hypoxic Conditions |
title_fullStr | Ruthenium(II)
Polypyridyl Complexes and Metronidazole
Derivatives: A Powerful Combination in the Design of Photoresponsive
Antibacterial Agents Effective under Hypoxic Conditions |
title_full_unstemmed | Ruthenium(II)
Polypyridyl Complexes and Metronidazole
Derivatives: A Powerful Combination in the Design of Photoresponsive
Antibacterial Agents Effective under Hypoxic Conditions |
title_short | Ruthenium(II)
Polypyridyl Complexes and Metronidazole
Derivatives: A Powerful Combination in the Design of Photoresponsive
Antibacterial Agents Effective under Hypoxic Conditions |
title_sort | ruthenium(ii)
polypyridyl complexes and metronidazole
derivatives: a powerful combination in the design of photoresponsive
antibacterial agents effective under hypoxic conditions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207323/ https://www.ncbi.nlm.nih.gov/pubmed/37163381 http://dx.doi.org/10.1021/acs.inorgchem.3c00214 |
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