A Dinuclear Ruthenium(II) Complex Excited by Near-Infrared Light through Two-Photon Absorption Induces Phototoxicity Deep within Hypoxic Regions of Melanoma Cancer Spheroids
Author(s) -
Ahtasham Raza,
Stuart A. Archer,
Simon D. Fairbanks,
Kirsty L. Smitten,
Stanley W. Botchway,
Jim A. Thomas,
Sheila MacNeil,
John W. Haycock
Publication year - 2020
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.9b11313
Subject(s) - phototoxicity , chemistry , photochemistry , spheroid , absorption (acoustics) , singlet oxygen , excited state , ruthenium , fluorescence , phosphorescence , biophysics , oxygen , optics , atomic physics , biochemistry , physics , organic chemistry , in vitro , biology , catalysis
The dinuclear photo-oxidizing Ru II complex [{Ru(TAP 2 )} 2 (tpphz)] 4+ (TAP = 1,4,5,8- tetraazaphenanthrene, tpphz = tetrapyrido[3,2- a :2',3'- c :3″,2''- h :2‴,3'''- j ]phenazine), 1 4+ , is readily taken up by live cells localizing in mitochondria and nuclei. In this study, the two-photon absorption cross section of 1 4+ is quantified and its use as a two-photon absorbing phototherapeutic is reported. It was confirmed that the complex is readily photoexcited using near-infrared, NIR, and light through two-photon absorption, TPA. In 2-D cell cultures, irradiation with NIR light at low power results in precisely focused phototoxicity effects in which human melanoma cells were killed after 5 min of light exposure. Similar experiments were then carried out in human cancer spheroids that provide a realistic tumor model for the development of therapeutics and phototherapeutics. Using the characteristic emission of the complex as a probe, its uptake into 280 μm spheroids was investigated and confirmed that the spheroid takes up the complex. Notably TPA excitation results in more intense luminescence being observed throughout the depth of the spheroids, although emission intensity still drops off toward the necrotic core. As 1 4+ can directly photo-oxidize DNA without the mediation of singlet oxygen or other reactive oxygen species, phototoxicity within the deeper, hypoxic layers of the spheroids was also investigated. To quantify the penetration of these phototoxic effects, 1 4+ was photoexcited through TPA at a power of 60 mW, which was progressively focused in 10 μm steps throughout the entire z -axis of individual spheroids. These experiments revealed that, in irradiated spheroids treated with 1 4+ , acute and rapid photoinduced cell death was observed throughout their depth, including the hypoxic region.
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