Synthesis and evaluation of chalcogenopyrylium dyes as potential sensitizers for the photodynamic therapy of cancer

A series of thiopyrylium (2), selenopyrylium (3), and telluropyrylium dyes (4) was prepared via the addition of Grignard reagents to either 2,6-di(4-d imethylamino)phenylchalcogenopyran-4-ones (5a) or 2-[4-(dimethylamino)pheny l] -6-phenylchalcogenopyran-4-ones (5b) followed by elimination and ion exc hange to give the chloride salts. The absorption spectra and quantum yields for singlet oxygen generation of these dyes suggested that the dyes would have utility as sensitizers for PDT. Selenopyrylium dyes 3a and 3d with qua ntum yields for singlet oxygen generation of 0.040 and 0.045, respectively, were phototoxic to Colo-26 cells in culture. The toxicity of the dyes 2-4 was evaluated in clonogenic assays of human carcinoma cell lines. Important ly, the presence of a sulfur, selenium, or tellurium heteroatom in the mole cules had no predictable impact on the toxicity of any particular dye set. Substituents at the 2-, 4-, and 6-positions of the dye had a much greater i mpact on cytotoxicity. The IC50 values determined in the clonogenic assays did not correlate with chemical properties in the dye molecules such as red uction potential or lipophilicity. Initial in vivo toxicity studies showed no toxicity for these dyes at dosages between 7.2 and 38 mu mol/kg in BALB/ c mice.