Monofunctional platinum(II) complexes of formulation cis-[Pt(NH3)2(L)Cl](NO3), where L is an imidazole base conjugated to 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) with emissive (L1 in 1) and nonemissive (L2 in 2) moieties were prepared and characterized, and their singlet oxygen-mediated photoinduced cytotoxicity was studied. The 1-methylimidazole (1-MeIm) complex 3 was prepared as a control and for structural characterization by X-ray crystallography. Complexes 1 and 2 showed strong visible absorption bands at 500 nm (ε = 2.7 × 104 M–1 cm–1) and 540 nm (1.4 × 104 M–1 cm–1). Complex 1 is emissive with a band at 510 nm (ΦF = 0.09) in 1% dimethyl sulfoxide/Dulbecco’s Modified Eagle’s Medium (pH 7.2). Singlet oxygen generation upon photoirradiation with visible light (400–700 nm) was evidenced from 1,3-diphenylisobenzofuran titration experiments showing significant photosensitizing ability of the BODIPY complexes. Both 1 and 2 were remarkably photocytotoxic in visible light (400–700 nm, 10 J cm–2) in skin keratinocyte HaCaT and breast cancer MCF-7 cells giving IC50 values in nanomolar concentration. The complexes were, however, essentially nontoxic to the cells in the dark (IC50 > 80 μM). Complex 2 having a diiodo-BODIPY unit is nonemissive but an efficient photosensitizer with high singlet oxygen generation ability in visible light (400–700 nm). Confocal microscopy using the emissive complex 1 showed significant mitochondrial localization of the complex. Cell death via apoptotic pathway was observed from the Annexin-V-FITC/PI assay. The formation of Pt-DNA adducts was evidenced from the binding experiments of the complexes 1 and 2 with 9-ethylguanine as a model nucleobase from 1H NMR and mass spectral studies.
Monofunctional imidazoplatin complexes having pendant photoactive BODIPY moieties as mitochondria-localizing anticancer agents are prepared and studied. They exhibit remarkable apoptotic photocytotoxicity in visible light (400−700 nm) in skin keratinocyte HaCaT and breast cancer MCF-7 cells by generating singlet oxygen as the reactive species, while being nontoxic in dark. The emisssive noniodo BODIPY complex showed mitochondrial localization, while its diiodo analogue displayed excellent PDT activity. 9-Ethylguanine addition showed monoadduct formation with replacement of one ammine ligand.
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