| Literature DB >> 32172564 |
Johannes Karges1, Franz Heinemann1,2, Marta Jakubaszek1,3, Federica Maschietto4, Chloé Subecz1, Mazzarine Dotou1, Robin Vinck1, Olivier Blacque2, Mickaël Tharaud5, Bruno Goud3, Emilio Viñuelas Zahı Nos6, Bernhard Spingler2, Ilaria Ciofini4, Gilles Gasser1.
Abstract
The utilization of photodynamic therapy (PDT) for the treatment of various types of cancer has gained increasing attention over the last decades. Despite the clinical success of approved photosensitizers (PSs), their application is sometimes limited due to poor water solubility, aggregation, photodegradation, and slow clearance from the body. To overcome these drawbacks, research efforts are devoted toward the development of metal complexes and especially Ru(II) polypyridine complexes based on their attractive photophysical and biological properties. Despite the recent research developments, the vast majority of complexes utilize blue or UV-A light to obtain a PDT effect, limiting the penetration depth inside tissues and, therefore, the possibility to treat deep-seated or large tumors. To circumvent these drawbacks, we present the first example of a DFT guided search for efficient PDT PSs with a substantial spectral red shift toward the biological spectral window. Thanks to this design, we have unveiled a Ru(II) polypyridine complex that causes phototoxicity in the very low micromolar to nanomolar range at clinically relevant 595 nm, in monolayer cells as well as in 3D multicellular tumor spheroids.Entities:
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Year: 2020 PMID: 32172564 DOI: 10.1021/jacs.9b13620
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419