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Tunable Emissive Ir(III) Benzimidazole‐quinoline Hybrids as Promising Theranostic Lead Compounds

Bioactive and luminescent cyclometallated Ir(III) complexes [Ir(ppy)(2) L1]Cl (1) and [Ir(ppy)(2) L2]Cl (2) containing a benzimidazole derivative (L1/L2) as auxiliary mimic of a nucleotide have been synthesised. The emissive properties of both complexes are conditioned by the nature of L1 and L2, re...

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Autores principales: Redrado, Marta, Miñana, Miriam, Coogan, Michael P., Concepción Gimeno, M., Fernández‐Moreira, Vanesa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796238/
https://www.ncbi.nlm.nih.gov/pubmed/35767349
http://dx.doi.org/10.1002/cmdc.202200244
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author Redrado, Marta
Miñana, Miriam
Coogan, Michael P.
Concepción Gimeno, M.
Fernández‐Moreira, Vanesa
author_facet Redrado, Marta
Miñana, Miriam
Coogan, Michael P.
Concepción Gimeno, M.
Fernández‐Moreira, Vanesa
author_sort Redrado, Marta
collection PubMed
description Bioactive and luminescent cyclometallated Ir(III) complexes [Ir(ppy)(2) L1]Cl (1) and [Ir(ppy)(2) L2]Cl (2) containing a benzimidazole derivative (L1/L2) as auxiliary mimic of a nucleotide have been synthesised. The emissive properties of both complexes are conditioned by the nature of L1 and L2, rendering an orange and a green emitter respectively. Both are highly emissive with quantum yield increasing in absence of oxygen up to 0.26 (1) and 0.36 (2), suggesting their phosphorescent character. Antiproliferative activity against lung cancer A549 cells increased up to 15 times upon irradiation conditions, reaching IC(50) values in the nanomolar range (0.3±0.09 μM (1) and 0.26±0.14 μM (2)) and pointing them as good PSs candidates for photodynamic therapy via (1)O(2) generation. Cellular biodistribution analysis by fluorescence microscopy suggest the lysosomes as the preferential accumulation organelle. Time‐resolved studies showed a greatly increased cellular emission lifetime compared to the solution values, indicating binding to macromolecules or cellular structures and restriction of collision and vibrational quenching.
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spelling pubmed-97962382022-12-30 Tunable Emissive Ir(III) Benzimidazole‐quinoline Hybrids as Promising Theranostic Lead Compounds Redrado, Marta Miñana, Miriam Coogan, Michael P. Concepción Gimeno, M. Fernández‐Moreira, Vanesa ChemMedChem Research Articles Bioactive and luminescent cyclometallated Ir(III) complexes [Ir(ppy)(2) L1]Cl (1) and [Ir(ppy)(2) L2]Cl (2) containing a benzimidazole derivative (L1/L2) as auxiliary mimic of a nucleotide have been synthesised. The emissive properties of both complexes are conditioned by the nature of L1 and L2, rendering an orange and a green emitter respectively. Both are highly emissive with quantum yield increasing in absence of oxygen up to 0.26 (1) and 0.36 (2), suggesting their phosphorescent character. Antiproliferative activity against lung cancer A549 cells increased up to 15 times upon irradiation conditions, reaching IC(50) values in the nanomolar range (0.3±0.09 μM (1) and 0.26±0.14 μM (2)) and pointing them as good PSs candidates for photodynamic therapy via (1)O(2) generation. Cellular biodistribution analysis by fluorescence microscopy suggest the lysosomes as the preferential accumulation organelle. Time‐resolved studies showed a greatly increased cellular emission lifetime compared to the solution values, indicating binding to macromolecules or cellular structures and restriction of collision and vibrational quenching. John Wiley and Sons Inc. 2022-07-13 2022-09-16 /pmc/articles/PMC9796238/ /pubmed/35767349 http://dx.doi.org/10.1002/cmdc.202200244 Text en © 2022 The Authors. ChemMedChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Redrado, Marta
Miñana, Miriam
Coogan, Michael P.
Concepción Gimeno, M.
Fernández‐Moreira, Vanesa
Tunable Emissive Ir(III) Benzimidazole‐quinoline Hybrids as Promising Theranostic Lead Compounds
title Tunable Emissive Ir(III) Benzimidazole‐quinoline Hybrids as Promising Theranostic Lead Compounds
title_full Tunable Emissive Ir(III) Benzimidazole‐quinoline Hybrids as Promising Theranostic Lead Compounds
title_fullStr Tunable Emissive Ir(III) Benzimidazole‐quinoline Hybrids as Promising Theranostic Lead Compounds
title_full_unstemmed Tunable Emissive Ir(III) Benzimidazole‐quinoline Hybrids as Promising Theranostic Lead Compounds
title_short Tunable Emissive Ir(III) Benzimidazole‐quinoline Hybrids as Promising Theranostic Lead Compounds
title_sort tunable emissive ir(iii) benzimidazole‐quinoline hybrids as promising theranostic lead compounds
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796238/
https://www.ncbi.nlm.nih.gov/pubmed/35767349
http://dx.doi.org/10.1002/cmdc.202200244
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