4.5 Article

Phosphorescent O2-Probes Based on Ir(III) Complexes for Bioimaging Applications

Journal

CHEMOSENSORS
Volume 11, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/chemosensors11050263

Keywords

oxygen sensing; iridium complexes; phosphorescence; hypoxia; bioimaging; phosphorescence lifetime imaging

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The design, synthesis, and investigation of new molecular oxygen probes for bioimaging, based on phosphorescent transition metal complexes, have been studied. Three new iridium complexes with different ligands have been synthesized and characterized. These complexes exhibited phosphorescence and showed potential for use in bioimaging experiments. Furthermore, they were found to be internalized into cancer cells and localized in mitochondria and lysosomes.
The design, synthesis, and investigation of new molecular oxygen probes for bioimaging, based on phosphorescent transition metal complexes are among the topical problems of modern chemistry and advanced bioimaging. Three new iridium [Ir(N boolean AND C)(2)(N boolean AND N)](+) complexes with cyclometallating 4-(pyridin-2-yl)-benzoic acid derivatives and different di-imine chelate ligands have been synthesized and characterized by mass spectrometry and NMR spectroscopy. The periphery of these complexes is decorated with three relatively small double-tail oligo(ethylene glycol) fragments. All these complexes exhibit phosphorescence; their photophysical properties have been thoroughly studied, and quantum chemical calculations of their photophysical properties were also performed. It turned out that the changes in the nature of the di-imine ligand greatly affected the character of the electronic transitions responsible for their emission. Two complexes in this series show the desired photophysical characteristics; they demonstrate appreciable quantum yield (14-15% in degassed aqueous solutions) and a strong response to the changes in oxygen concentration, ca. three-fold increase in emission intensity, and an excited state lifetime upon deaeration of the aqueous solution. The study of their photophysical properties in model biological systems (buffer solutions containing fetal bovine serum-FBS) and cytotoxicity assays (MTT) showed that these complexes satisfy the requirements for application in bioimaging experiments. It was found that these molecular probes are internalized into cultured cancer cells and localized mainly in mitochondria and lysosomes. Phosphorescent lifetime imaging (PLIM) experiments showed that under hypoxic conditions in cells, a 1.5-fold increase in the excitation state lifetime was observed compared to aerated cells, suggesting the applicability of these complexes for the analysis of hypoxia in biological objects.

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