首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Photodynamic effects of isosteric water-soluble phthalocyanines on human nasopharynx KB carcinoma cells.
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Photodynamic effects of isosteric water-soluble phthalocyanines on human nasopharynx KB carcinoma cells.

机译:等距的水溶性酞菁对人鼻咽KB癌细胞的光动力作用。

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摘要

The photodynamic activity of water-soluble cationic zinc(II) phthalocyanines using human nasopharynx carcinoma (KB cells) was investigated. A sulfur-linked cationic dye, named: 2,9(10),16(17),23(24)-tetrakis[(2-trimethylammonium)ethylsulfanyl]phthalocyaninat ozinc(II) tetraioidide (13) is the most active of four sensitizer assays and shows a singlet oxygen quantum yield of 0.58 and a higher bathochromic shift of 10 nm for the Q-band as compared with the oxygen-linked cationic aliphatic phthalocyanine: 2,9(10),16(17),23(24)-tetrakis[(2-trimethylammonium)ethoxy]phthalocyaninatozinc(I I) tetraioidide (11) and the best photo-stability in water in comparison with their tetra-alpha-substituted counterparts 1,8(11),15(18),22(25)-tetrakis[(2-trimethylammonium)ethoxy]phthalocyaninatozinc(I I) tetraioidide (12) and 1,8(11),15(18),22(25)-tetrakis[(2-trimethylammonium)ethylsulfanyl]phthalocyaninat ozinc(II) tetraioidide (14). Phthalocyanine 13, partially localized in lysosomes, led to cell photoinactivation in a concentration- and light dose-dependent manner. After photodynamic treatment, compound 13 induced an apoptotic response--as indicated by morphological cell changes--an increase in the activity of caspase-3 and the cleavage of poly-ADP-ribose-polymerase substrate (PARP).
机译:研究了使用人鼻咽癌(KB细胞)的水溶性阳离子锌(II)酞菁的光动力活性。一种硫磺连接的阳离子染料,名为:2,9(10),16(17),23(24)-四[[2-三甲基铵)乙基硫烷基]酞菁锌四碘化物(II)(13)是活性最高的四种敏化剂分析,与氧连接的阳离子脂肪族酞菁相比,Q带的单重态氧量子产率为0.58,更高的红移为10 nm:2,9(10),16(17),23(24) )-四[[(2-三甲基铵)乙氧基]邻苯二甲酰基萘并锌(II)四碘化物(11)以及与四-α-取代的对应物1,8(11),15(18),22相比在水中具有最佳的光稳定性(25)-四[[(2-三甲基铵)乙氧基]邻苯二甲酸氰基锌(II)四碘化物(12)和1,8(11),15(18),22(25)-四[[(2-三甲基铵)乙硫基]酞菁锌(II)四碘化物(14)。酞菁13部分位于溶酶体中,以浓度和光剂量依赖性方式导致细胞光灭活。光动力学处理后,化合物13诱导了凋亡反应(如形态细胞变化所表明的),胱天蛋白酶3的活性增加,聚ADP核糖聚合酶底物(PARP)裂解。

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