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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >A set of highly water-soluble tetraethyleneglycol-substituted Zn(ii) phthalocyanines: Synthesis, photochemical and photophysical properties, interaction with plasma proteins and in vitro phototoxicity
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A set of highly water-soluble tetraethyleneglycol-substituted Zn(ii) phthalocyanines: Synthesis, photochemical and photophysical properties, interaction with plasma proteins and in vitro phototoxicity

机译:一组高度水溶性的四乙二醇取代的Zn(ii)酞菁锌:合成,光化学和光物理性质,与血浆蛋白的相互作用以及体外光毒性

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摘要

Three Zn(ii) phthalocyanines substituted by hydroxyl-terminated tetraethylene glycol chains have been synthesized. In order to evaluate the potential of these highly water-soluble phthalocyanines as type II-photosensitisers for photodynamic therapy, their structure-activity relationship was assessed by determining relevant photophysical and photochemical properties, such as their aggregation behaviour in aqueous buffers, their fluorescence properties and their efficiency with regard to the generation of singlet oxygen. In addition, evidence for a negligible interaction with plasma proteins in undiluted human plasma was obtained using a recently developed bioanalytical method and compared with the fluorescence quenching approach. These results combined with in vitro data regarding the phototoxicity of these phthalocyanines against HT-29 cancer cells provide evidence for the relevance of the non-peripherally substituted derivative for further in vivo investigations.
机译:已合成了三个被羟基封端的四甘醇链取代的Zn(ii)酞菁。为了评估这些高度水溶性的酞菁作为II型光敏剂用于光动力疗法的潜力,通过确定相关的光物理和光化学特性(例如它们在水性缓冲液中的聚集行为,它们的荧光特性和它们在产生单线态氧方面的效率。另外,使用最近开发的生物分析方法获得了与未稀释的人血浆中血浆蛋白相互作用微不足道的证据,并与荧光猝灭方法进行了比较。这些结果与有关这些酞菁对HT-29癌细胞的光毒性的体外数据相结合,为非外围取代衍生物与进一步的体内研究相关性提供了证据。

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