Multinuclear Ru(II) and Ir(III) decorated tetraphenylporphyrins as efficient PDT agents

Justo Cabrera-González, Jorge Soriano, Robert Conway-Kenny, Junsi Wang, Yue Lu, Jianzhang Zhao, Carme Nogués, Sylvia M. Draper

Producción científica: Contribución a una revistaArtículoInvestigación

15 Citas (Scopus)

Resumen

© 2019 The Royal Society of Chemistry. Two novel porphyrin-core systems were prepared by Sonogashira cross-coupling of the terminal alkyne groups of meso-tetra(4-ethynylphenyl)porphyrin-Zn(ii) (P-1) with halogenated Ru(ii)- or Ir(iii)-phenanthroline complexes. The resulting compounds (P-Ru and P-Ir) were spectroscopically characterised and their photophysical properties were investigated (λem 625, 665 nm; τT 339.6 μs (P-Ru) and λem 530, 612, 664 nm; τT 396.6 μs (P-Ir)). Nanosecond time-resolved transient absorption studies were used to explore the 3MLCT nature of the triplet excited states, and the singlet oxygen quantum yields were determined (ΦΔ 44.8 (P-Ru), 33.2 (P-Ir)%). The subcellular uptake of P-Ru and P-Ir and their application as photosensitisers (PS) in photodynamic therapy (PDT) were explored due to their solution photophysics and absence of dark toxicity. Upon irradiation (λexc = 620-630 nm; 10 min; 33 J cm-2), both P-Ru and P-Ir killed 90% of SKBR-3 cells at 1 μM. Notably P-Ru induced a 77% decrease in cell viability at only 0.25 μM.
Idioma originalInglés
Páginas (desde-hasta)3287-3296
PublicaciónBiomaterials Science
Volumen7
DOI
EstadoPublicada - 1 ago 2019

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