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Exploring Titanium(IV) Complexes as Potential Antimicrobial Compounds

Due to the rapid mutation of pathogenic microorganisms, drug-resistant superbugs have evolved. Antimicrobial-resistant germs may share their resistance genes with other germs, making them untreatable. The search for more combative antibiotic compounds has led researchers to explore metal-based strat...

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Autores principales: Rodríguez, Israel, Fernández-Vega, Lauren, Maser-Figueroa, Andrea N., Sang, Branlee, González-Pagán, Patricia, Tinoco, Arthur D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8868518/
https://www.ncbi.nlm.nih.gov/pubmed/35203761
http://dx.doi.org/10.3390/antibiotics11020158
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author Rodríguez, Israel
Fernández-Vega, Lauren
Maser-Figueroa, Andrea N.
Sang, Branlee
González-Pagán, Patricia
Tinoco, Arthur D.
author_facet Rodríguez, Israel
Fernández-Vega, Lauren
Maser-Figueroa, Andrea N.
Sang, Branlee
González-Pagán, Patricia
Tinoco, Arthur D.
author_sort Rodríguez, Israel
collection PubMed
description Due to the rapid mutation of pathogenic microorganisms, drug-resistant superbugs have evolved. Antimicrobial-resistant germs may share their resistance genes with other germs, making them untreatable. The search for more combative antibiotic compounds has led researchers to explore metal-based strategies centered on perturbing the bioavailability of essential metals in microbes and examining the therapeutic potential of metal complexes. Given the limited knowledge on the application of titanium(IV), in this work, eight Ti(IV) complexes and some of their corresponding ligands were screened by the Community for Open Antimicrobial Drug Discovery for antimicrobial activity. The compounds were selected for evaluation because of their low cytotoxic/antiproliferative behavior against a human non-cancer cell line. At pH 7.4, these compounds vary in terms of their solution stability and ligand exchange lability; therefore, an assessment of their solution behavior provides some insight regarding the importance of the identity of the metal compound to the antimicrobial therapeutic potential. Only one compound, Ti(deferasirox)(2), exhibited promising inhibitory activity against the Gram-positive bacteria methicillin-resistant Staphylococcus aureus and minimal toxicity against human cells. The ability of this compound to undergo transmetalation with labile Fe(III) sources and, as a consequence, inhibit Fe bioavailability and ribonucleotide reductase is evaluated as a possible mechanism for its antibiotic effect.
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spelling pubmed-88685182022-02-25 Exploring Titanium(IV) Complexes as Potential Antimicrobial Compounds Rodríguez, Israel Fernández-Vega, Lauren Maser-Figueroa, Andrea N. Sang, Branlee González-Pagán, Patricia Tinoco, Arthur D. Antibiotics (Basel) Article Due to the rapid mutation of pathogenic microorganisms, drug-resistant superbugs have evolved. Antimicrobial-resistant germs may share their resistance genes with other germs, making them untreatable. The search for more combative antibiotic compounds has led researchers to explore metal-based strategies centered on perturbing the bioavailability of essential metals in microbes and examining the therapeutic potential of metal complexes. Given the limited knowledge on the application of titanium(IV), in this work, eight Ti(IV) complexes and some of their corresponding ligands were screened by the Community for Open Antimicrobial Drug Discovery for antimicrobial activity. The compounds were selected for evaluation because of their low cytotoxic/antiproliferative behavior against a human non-cancer cell line. At pH 7.4, these compounds vary in terms of their solution stability and ligand exchange lability; therefore, an assessment of their solution behavior provides some insight regarding the importance of the identity of the metal compound to the antimicrobial therapeutic potential. Only one compound, Ti(deferasirox)(2), exhibited promising inhibitory activity against the Gram-positive bacteria methicillin-resistant Staphylococcus aureus and minimal toxicity against human cells. The ability of this compound to undergo transmetalation with labile Fe(III) sources and, as a consequence, inhibit Fe bioavailability and ribonucleotide reductase is evaluated as a possible mechanism for its antibiotic effect. MDPI 2022-01-26 /pmc/articles/PMC8868518/ /pubmed/35203761 http://dx.doi.org/10.3390/antibiotics11020158 Text en © 2022 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
Rodríguez, Israel
Fernández-Vega, Lauren
Maser-Figueroa, Andrea N.
Sang, Branlee
González-Pagán, Patricia
Tinoco, Arthur D.
Exploring Titanium(IV) Complexes as Potential Antimicrobial Compounds
title Exploring Titanium(IV) Complexes as Potential Antimicrobial Compounds
title_full Exploring Titanium(IV) Complexes as Potential Antimicrobial Compounds
title_fullStr Exploring Titanium(IV) Complexes as Potential Antimicrobial Compounds
title_full_unstemmed Exploring Titanium(IV) Complexes as Potential Antimicrobial Compounds
title_short Exploring Titanium(IV) Complexes as Potential Antimicrobial Compounds
title_sort exploring titanium(iv) complexes as potential antimicrobial compounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8868518/
https://www.ncbi.nlm.nih.gov/pubmed/35203761
http://dx.doi.org/10.3390/antibiotics11020158
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