Photodynamic therapy delivers more targeted cell killing than classical chemotherapy. It uses light-absorbing compounds, photosensitizers (PSs), to generate lethal reactive oxygen species (ROS) at sites of localized irradiation. Transition metal complexes are attractive PSs due to their photostability, visible-light absorption, and high ROS yields. Here, we introduce a low-molecular weight, photostable iridium complex, [Ir(thpy)(benz)]Cl, , that localizes to the Golgi apparatus, mitochondria, and endoplasmic reticulum, absorbs visible light, phosphoresces strongly, generates O with 43% yield, and undergoes cellular elimination after 24 h. shows low dark toxicity and under remarkably low doses (3 min, 20-30 mJ s cm) of 405 or 455 nm light, it causes killing of bladder (EJ), malignant melanoma (A375), and oropharyngeal (OPSCC72) cancer cells, with high phototoxic indices > 100-378. is also an efficient PS in 3D melanoma spheroids, with repeated short-time irradiation causing cumulative killing.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11440503 | PMC |
http://dx.doi.org/10.1021/acs.jmedchem.4c00869 | DOI Listing |
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