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Platinum Cyclooctadiene Complexes with Activity against Gram‐positive Bacteria
Antimicrobial resistance is a looming health crisis, and it is becoming increasingly clear that organic chemistry alone is not sufficient to continue to provide the world with novel and effective antibiotics. Recently there has been an increased number of reports describing promising antimicrobial p...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596843/ https://www.ncbi.nlm.nih.gov/pubmed/34018686 http://dx.doi.org/10.1002/cmdc.202100157 |
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author | Frei, Angelo Ramu, Soumya Lowe, Gabrielle J. Dinh, Hue Semenec, Lucie Elliott, Alysha G. Zuegg, Johannes Deckers, Anke Jung, Nicole Bräse, Stefan Cain, Amy K. Blaskovich, Mark A. T. |
author_facet | Frei, Angelo Ramu, Soumya Lowe, Gabrielle J. Dinh, Hue Semenec, Lucie Elliott, Alysha G. Zuegg, Johannes Deckers, Anke Jung, Nicole Bräse, Stefan Cain, Amy K. Blaskovich, Mark A. T. |
author_sort | Frei, Angelo |
collection | PubMed |
description | Antimicrobial resistance is a looming health crisis, and it is becoming increasingly clear that organic chemistry alone is not sufficient to continue to provide the world with novel and effective antibiotics. Recently there has been an increased number of reports describing promising antimicrobial properties of metal‐containing compounds. Platinum complexes are well known in the field of inorganic medicinal chemistry for their tremendous success as anticancer agents. Here we report on the promising antibacterial properties of platinum cyclooctadiene (COD) complexes. Amongst the 15 compounds studied, the simplest compounds Pt(COD)X(2) (X=Cl, I, Pt1 and Pt2) showed excellent activity against a panel of Gram‐positive bacteria including vancomycin and methicillin resistant Staphylococcus aureus. Additionally, the lead compounds show no toxicity against mammalian cells or haemolytic properties at the highest tested concentrations, indicating that the observed activity is specific against bacteria. Finally, these compounds showed no toxicity against Galleria mellonella at the highest measured concentrations. However, preliminary efficacy studies in the same animal model found no decrease in bacterial load upon treatment with Pt1 and Pt2. Serum exchange studies suggest that these compounds exhibit high serum binding which reduces their bioavailability in vivo, mandating alternative administration routes such as e. g. topical application. |
format | Online Article Text |
id | pubmed-8596843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85968432021-11-22 Platinum Cyclooctadiene Complexes with Activity against Gram‐positive Bacteria Frei, Angelo Ramu, Soumya Lowe, Gabrielle J. Dinh, Hue Semenec, Lucie Elliott, Alysha G. Zuegg, Johannes Deckers, Anke Jung, Nicole Bräse, Stefan Cain, Amy K. Blaskovich, Mark A. T. ChemMedChem Communications Antimicrobial resistance is a looming health crisis, and it is becoming increasingly clear that organic chemistry alone is not sufficient to continue to provide the world with novel and effective antibiotics. Recently there has been an increased number of reports describing promising antimicrobial properties of metal‐containing compounds. Platinum complexes are well known in the field of inorganic medicinal chemistry for their tremendous success as anticancer agents. Here we report on the promising antibacterial properties of platinum cyclooctadiene (COD) complexes. Amongst the 15 compounds studied, the simplest compounds Pt(COD)X(2) (X=Cl, I, Pt1 and Pt2) showed excellent activity against a panel of Gram‐positive bacteria including vancomycin and methicillin resistant Staphylococcus aureus. Additionally, the lead compounds show no toxicity against mammalian cells or haemolytic properties at the highest tested concentrations, indicating that the observed activity is specific against bacteria. Finally, these compounds showed no toxicity against Galleria mellonella at the highest measured concentrations. However, preliminary efficacy studies in the same animal model found no decrease in bacterial load upon treatment with Pt1 and Pt2. Serum exchange studies suggest that these compounds exhibit high serum binding which reduces their bioavailability in vivo, mandating alternative administration routes such as e. g. topical application. John Wiley and Sons Inc. 2021-07-08 2021-10-15 /pmc/articles/PMC8596843/ /pubmed/34018686 http://dx.doi.org/10.1002/cmdc.202100157 Text en © 2021 The Authors. ChemMedChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Frei, Angelo Ramu, Soumya Lowe, Gabrielle J. Dinh, Hue Semenec, Lucie Elliott, Alysha G. Zuegg, Johannes Deckers, Anke Jung, Nicole Bräse, Stefan Cain, Amy K. Blaskovich, Mark A. T. Platinum Cyclooctadiene Complexes with Activity against Gram‐positive Bacteria |
title | Platinum Cyclooctadiene Complexes with Activity against Gram‐positive Bacteria |
title_full | Platinum Cyclooctadiene Complexes with Activity against Gram‐positive Bacteria |
title_fullStr | Platinum Cyclooctadiene Complexes with Activity against Gram‐positive Bacteria |
title_full_unstemmed | Platinum Cyclooctadiene Complexes with Activity against Gram‐positive Bacteria |
title_short | Platinum Cyclooctadiene Complexes with Activity against Gram‐positive Bacteria |
title_sort | platinum cyclooctadiene complexes with activity against gram‐positive bacteria |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596843/ https://www.ncbi.nlm.nih.gov/pubmed/34018686 http://dx.doi.org/10.1002/cmdc.202100157 |
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