...
首页> 外文期刊>Bioorganic and Medicinal Chemistry >Synthesis and photodynamic activity of zinc(II) phthalocyanine derivatives bearing methoxy and trifluoromethylbenzyloxy substituents in homogeneous and biological media.
【24h】

Synthesis and photodynamic activity of zinc(II) phthalocyanine derivatives bearing methoxy and trifluoromethylbenzyloxy substituents in homogeneous and biological media.

机译:在均相和生物介质中带有甲氧基和三氟甲基苄氧基取代基的锌(II)酞菁衍生物的合成和光动力活性。

获取原文
获取原文并翻译 | 示例

摘要

Two zinc(II) phthalocyanines bearing either four methoxy (ZnPc 3) or trifluoromethylbenzyloxy (ZnPc 4) substituents have been synthesized by a two-step procedure starting from 4-nitrophthalonitrile. Absorption and fluorescence spectroscopic studies were analyzed in different media. These compounds are essentially non-aggregated in the organic solvent. Fluorescence quantum yields (varphi(F)) of 0.26 for ZnPc 3 and 0.25 for ZnPc 4 were calculated in tetrahydrofuran (THF). The photodynamic activity of these compounds was compared in both THF containing photooxidizable substrates and in vitro on Hep-2 human larynx-carcinoma cell line. The production of singlet molecular oxygen, O(2)((1)Delta(g)), was determined using 9,10-dimethylanthracene yielding values of approximately 0.56 for both sensitizers. Under these conditions, the addition of beta-carotene (Car) suppresses the O(2)((1)Delta(g))-mediated photooxidation. In biological medium, no dark cytotoxicity was found for cells incubated with 0.1muM of phthalocyanines 3 and 4 for 24h. However, under similar conditions 0.5muM of ZnPc 4 was toxic (70% cell survival). The uptake into Hep-2 cells was evaluated using 0.1muM of sensitizer, reaching values of approximately 0.05nmol/10(6) cells after 3h of incubation at 37 degrees C. The cell survival after irradiation of the cultures with visible light was dependent upon both light exposure level and intracellular sensitizer concentration. A higher photocytotoxic effect was found for ZnPc 3 with respect to 4 (32%/70% cell survival after 15min of irradiation). Also, these studies were performed treating the cells with 0.5muM of ZnPc 3. In this case, an increase in the uptake ( approximately 0.28nmol/10(6) cells) was observed, which is accompanied by a higher photocytotoxic activity (20% cell survival). These results show that even though both sensitizer present similar photophysical properties in homogeneous medium, the photodynamic behavior in cellular media can significantly be changed.
机译:从4-硝基邻苯二甲腈开始,通过两个步骤合成了带有四个甲氧基(ZnPc 3)或三氟甲基苄氧基(ZnPc 4)取代基的两个锌(II)酞菁。在不同的介质中分析了吸收和荧光光谱研究。这些化合物在有机溶剂中基本上是非聚集的。在四氢呋喃(THF)中计算得出ZnPc 3的荧光量子产率(varphi(F))为0.26,ZnPc 4的荧光量子产率为0.25。在含有THF的可光氧化底物和体外在Hep-2人喉癌细胞系中比较了这些化合物的光动力活性。使用两种增感剂的9,10-二甲基蒽产率约为0.56,确定了单线态分子氧O(2)((1)Delta(g))的产生。在这些条件下,添加β-胡萝卜素(Car)会抑制O(2)((1)Delta(g))介导的光氧化作用。在生物培养基中,对于与0.1μM酞菁3和4孵育24小时的细胞,没有发现暗细胞毒性。但是,在类似条件下,0.5μMZnPc 4具有毒性(70%的细胞存活率)。在37°C下孵育3小时后,使用0.1μM敏化剂评估Hep-2细胞的摄取,达到约0.05nmol / 10(6)细胞的值。培养物在可见光照射后的存活率取决于光照水平和细胞内敏化剂浓度。发现ZnPc 3相对于4具有更高的光细胞毒性作用(照射15分钟后细胞存活率为32%/ 70%)。此外,这些研究还用0.5μM的ZnPc 3处理细胞。在这种情况下,观察到摄取增加(约0.28nmol / 10(6)细胞),同时伴随着更高的光细胞毒性活性(20%)。细胞存活率)。这些结果表明,即使两种敏化剂在均质介质中均表现出相似的光物理性质,但在细胞介质中的光动力学行为仍可以显着改变。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号