Selenorhodamine photosensitizers with the Texas-red core for photodynamic therapy of cancer cells.

We examined two selenorhodamines with amide and thioamide functionality at the 5-position of a 9-(2-thienyl) substituent on the selenoxanthylium analogue of the Texas-red core for their potential as photosensitizers for photodynamic therapy (PDT) in P-glycoprotein (P-gp)-expressing Colo-26 cells. These compounds were examined for their photophysical properties (absorption, fluorescence, and ability to generate singlet oxygen), for their uptake into Colo-26 cells in the absence or presence of verapamil, for their dark and phototoxicity toward Colo-26 cells, and for their co-localization with mitochondrial-specific agents in Colo-26 cells. Both compounds were extremely effective photosensitizers with values of EC 50 ⩽ 4 × 10 −8 M toward Colo-26 cells with 1.0 J cm −2 laser light delivered at 630 ± 2 nm. [ABSTRACT FROM AUTHOR]