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首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Interaction of aluminum phthalocyanine with aziridinyl quinone in biomimicking micellar microenvironment for the application in photodynamic therapy: Effect of micellar hydration
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Interaction of aluminum phthalocyanine with aziridinyl quinone in biomimicking micellar microenvironment for the application in photodynamic therapy: Effect of micellar hydration

机译:铝酞菁与叠氮基醌在仿生胶束微环境中的相互作用在光动力疗法中的应用:胶束水化的影响

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Aluminum phthalocyanine tetrasulphonate (AlPcS4) is a well characterized water soluble phthalocyanine dye having structural similarities with porphyrin and has immense applications as a photosensitizer in photodynamic therapy (PDT). The present article embodies the exploration of physicochemical properties of PDT active AlPcS4 and its interaction with DNA alkylating quinone in biomimicking micellar microenvironments to overcome the limitation of PDT that is caused by the hypoxic nature of solid tumor. tN-vis absorption, steady state emission and time resolved fluorescence spectroscopy reveal that the AlPcS4 does not undergo considerable interaction with anionic SDS as well as uncharged Triton X-100 micelle, whereas in case of the series of a cationic surfactant (DTAB, TTAB, CTAB) it shows a significant columbic attraction toward the positively charged head group of the surfactant molecule. In premicellar concentration, surfactant induced aggregation of the probe molecule is observed, which subsequently disaggregates into its monomeric form above critical micellar concentration. The anionic dye localizes itself in the Stern layer of cationic micelles. The escalation of the fluorescence anisotropy value (r) with increase in the surfactant concentration is explained by the rise in compactness around the probe with increasing chain length of the cationic surfactant. However, the compactness has a reverse effect on the extent of water penetration or micellar hydration, which in turn decreases the polarity of microenvironment in the Stern layer. The fully micellized PDT active AlPcS4 experiences stronger interaction with DNA alkylating quinone in confined medium as compared to the aqueous solution and the above said interaction intensifies with decrease in the micellar hydration. This spectroscopic research described herein may provide relevant addition to the usefulness of this bioactive dye-quinone system for the application in photodynamic therapy. (C) 2015 Elsevier B.V. All rights reserved.
机译:酞菁铝四磺酸铝(AlPcS4)是一种特征明确的水溶性酞菁染料,与卟啉具有相似的结构,在光动力疗法(PDT)中作为光敏剂具有广阔的应用前景。本文体现了PDT活性AlPcS4的理化性质及其在模拟胶束微环境中与DNA烷基化醌的相互作用的探索,以克服由实体瘤的低氧性引起的PDT的局限性。 tN可见吸收,稳态发射和时间分辨荧光光谱表明,AlPcS4与阴离子SDS以及不带电的Triton X-100胶束没有发生显着的相互作用,而在一系列阳离子表面活性剂(DTAB,TTAB, CTAB)对表面活性剂分子带正电的头基显示出显着的哥伦布吸引力。在胶束前浓度下,观察到表面活性剂诱导的探针分子聚集,随后在临界胶束浓度以上聚集成单体形式。阴离子染料自身定位在阳离子胶束的斯特恩层中。随着表面活性剂浓度的增加,荧光各向异性值(r)的增加可以解释为,随着阳离子表面活性剂链长的增加,探针周围的紧密度增加。然而,紧密度对水渗透或胶束水合的程度具有相反的影响,这继而降低了斯特恩层中微环境的极性。与水溶液相比,完全胶束化的PDT活性AlPcS4与受限介质中的DNA烷基化醌具有更强的相互作用,并且上述相互作用随着胶束水合的减少而增强。本文所述的光谱研究可以为该生物活性染料-醌系统在光动力疗法中的应用的有用性提供相关的补充。 (C)2015 Elsevier B.V.保留所有权利。

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