Lysosome Targeting Bis-terpyridine Ruthenium(II) Complexes: Photophysical Properties and <i>In Vitro</i> Photodynamic Therapy

Abstract

Three heteroleptic bis-terpyridine ruthenium(II) complexes (<b>Ru1-Ru3</b>) [Ru(tpy-R₁)(tpy-R₂)]²⁺ (tpy = 2,2':6',2″-terpyridine, R₁/R₂ = phenyl, 4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}phenyl, pyren-1-yl, or 4-phenyl-BODIPY (boron dipyrromethene)) were synthesized and investigated for their potential applications as photosensitizers (PSs) for photodynamic therapy. All complexes displayed broad and intense absorption band in the green spectral regions (450-600 nm), which arose from the spin-allowed charge-transfer transitions mixed with ligand-localized ¹π,π* transitions. All complexes show weak green emission at 513-549 nm and/or even weaker red emission at 646-674 nm at room temperature depending on the excitation wavelength and the solvent used. Incorporating the BODIPY motif to the 4'-position of one of the tpy ligands in <b>Ru2</b> and <b>Ru3</b> drastically prolonged the lifetimes of the lowest triplet excited states (T₁) of <b>Ru2</b> and <b>Ru3</b> to tens of microseconds. This promoted the singlet oxygen formation sensitized by <b>Ru2</b> and <b>Ru3</b> upon green light activation, which in turn induced significant photocytotoxicity toward the A549 human lung cancer cell line with an EC₅₀ value of 1.50 μM for <b>Ru2</b> and 7.41 μM for <b>Ru3</b> under 0.48 J·cm^-2 500 nm light irradiation. Laser confocal scanning microscopy imaging revealed that <b>Ru2</b> mainly distributed to lysosomes upon cell uptake. Upon 500 nm light activation, <b>Ru2</b> induced lysosomal damage and subsequent mitochondrial membrane potential decrease. The dominant cell death pathway was apoptosis. These results demonstrated the potential utilization of [Ru(tpy-R₁)(tpy-R₂)]²⁺ complexes as PSs for PDT.