Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1784860437683109888 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9796238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT redradomarta tunableemissiveiriiibenzimidazolequinolinehybridsaspromisingtheranosticleadcompounds AT minanamiriam tunableemissiveiriiibenzimidazolequinolinehybridsaspromisingtheranosticleadcompounds AT cooganmichaelp tunableemissiveiriiibenzimidazolequinolinehybridsaspromisingtheranosticleadcompounds AT concepciongimenom tunableemissiveiriiibenzimidazolequinolinehybridsaspromisingtheranosticleadcompounds AT fernandezmoreiravanesa tunableemissiveiriiibenzimidazolequinolinehybridsaspromisingtheranosticleadcompounds |