| Literature DB >> 30985041 |
Alessia Colombo1, Mattia Fontani1, Claudia Dragonetti1, Dominique Roberto1, J A Gareth Williams2, Rossella Scotto di Perrotolo3, Francesca Casagrande3, Sara Barozzi3, Simona Polo3,4.
Abstract
Curcumin has chemopreventative properties against a variety of tumours, but has poor bioavailability. Here, two new bis-cyclometallated iridium(III) complexes have been prepared, featuring the natural product curcumin (CUR) or its reduced form, tetrahydrocurcumin (THC), as bidentate, anionic O O-binding ligands. The iridium THC complex is highly luminescent in deoxygenated solution and efficiently generates singlet oxygen under aerated conditions, whereas in the CUR analogue, other non-radiative decay pathways are competitive. The complexes are rapidly taken up by a variety of human tumour cell lines from solutions of micromolar concentration. They show negligible cytotoxicity in the absence of irradiation. When briefly irradiated with visible light, Ir-THC becomes highly phototoxic, inducing rapid apoptosis within 2 h. The results show the high potential of such complexes as sensitizers in photodynamic therapy (PDT).Entities:
Keywords: anticancer agents; curcumin; imaging agents; iridium; natural products; photodynamic therapy; tetrahydrocurcumin
Year: 2019 PMID: 30985041 DOI: 10.1002/chem.201901527
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236