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Comparative Study
. 2011 Nov;46(11):5532-9.
doi: 10.1016/j.ejmech.2011.09.014. Epub 2011 Sep 16.

Synthesis and comparative photodynamic properties of two isosteric alkyl substituted zinc(II) phthalocyanines

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Comparative Study

Synthesis and comparative photodynamic properties of two isosteric alkyl substituted zinc(II) phthalocyanines

Gabriela A Gauna et al. Eur J Med Chem. 2011 Nov.

Abstract

The synthesis and photophysical parameters of two novel isosteric cationic zinc(II) phthalocyanines: 2,9(10),16(17),23(24)-tetrakis[(N-butyl-N-methylammoniumethylsulfanyl]phthalocyaninatozinc(II) tetraiodide (6) and 2,9(10),16(17),23(24)-tetrakis[(N-dibutyl-N-methylammonium)ethoxy]phthalocyaninatozinc(II) tetraiodide (7) were investigated. Maximum absorption values were 686.5 nm and 678 nm for 6 and 7, respectively, whereas singlet molecular oxygen generation was 0.42 and 0.67, respectively. The photodynamic effect and the cellular uptake of both phthalocyanines were evaluated on human nasopharynx KB carcinoma cells. After light exposure, phthalocyanine 6 showed a higher cytotoxic activity than 7. In addition, a higher intracellular uptake of 6 and a preferential localization within lysosomes were demonstrated. The production of a greater amount of reactive oxygen species after phthalocyanine 6 irradiation would be responsible for its potent phototoxic action on KB cells.

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