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Probing the temperature-dependent changes of the interfacial hydration and viscosity of Tween20: cholesterol (1:1) niosome membrane using fisetin as a fluorescent molecular probe

机译:探讨互相水合和吐温粘度的温度依赖性变化:胆固醇(1:1)定位膜作为荧光分子探针的胆固醇(1:1)定位膜

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A detailed photophysical study of fisetin in a Tween20 : cholesterol (1 : 1) niosome membrane has been carried out. Fisetin is found to partition well into the Tween20 : cholesterol (1 : 1) niosome membrane at low temperature (Kp = 2.7 104 M 1 at 10 1C). Cetylpyridinium chloride quenching study confirms the location of fisetin molecules in the interfacial domain of Tween20 : cholesterol (1 : 1) niosome membrane. The emission from the prototropic forms of fisetin (neutral form, excited state anion, ground state anion and phototautomer form) is found to sensitively reflect the local heterogeneities in Tween20 : cholesterol (1 : 1) niosome membrane. The shift in anionic emission maximum with variation in temperature shows the sensitivity of fisetin towards water accessibility at the interfacial domain of Tween20 : cholesterol (1 : 1) niosome membrane. Zeta potential value confirms that there is no role of surface charge in the multiple prototropism of fisetin in Tween20 : cholesterol (1 : 1) niosome membrane. The microviscosity changes with temperature, as reflected in fluorescence anisotropy values of fisetin phototautomeric species FT*, give information about the temperature-induced changes in the motional resistance offered by the interfacial domain of the niosomal membrane to small molecules. A temperature-dependent fluorescence lifetime study confirms the distribution of FT* in the two different sites of niosomal interfacial domain, i. e. water-deficient inner site and water-accessible outer site. This heterogeneity in distribution of FT* is further confirmed through time-resolved fluorescence anisotropy decay resulting in two different rotational time constants (faster component of B1.04 ns originates from water-accessible outer site and slower component of B16.50 ns originates from water-deficient inner site). The interfacial location of fisetin in Tween20: cholesterol (1 : 1) niosome membrane has an important implication with regards to antioxidant activity as confirmed from a DPPH radical scavenging study.
机译:在吐温中的Fisetin细致的表现细物理研究:胆固醇(1:1)定位膜已经进行。发现Fisetin在低温下分配进入Tween20:胆固醇(1:1)定位膜(在10 1℃下Kp = 2.7104m 1)。十六烷嘧啶猝灭研究证实了在Tween20的界面结构域中的Fisetin分子的位置:胆固醇(1:1)定位膜。发现Fisetin(中性形式,激发态阴离子,研磨状态阴离子和光液体形式)的发射敏感地反映了Tween20:胆固醇(1:1)定位膜中的局部异质性。阴离子发射最大值的变化,温度变化表明,Fisetin在Tween20:胆固醇(1:1)定位膜的界面结构域中的水可均力的敏感性。 Zeta潜在值证实,在Tween20中Fisetin的多种原型中没有表面电荷的作用:胆固醇(1:1)定位膜。微粘性随温度的变化,如Fisetin光学型物质FT *的荧光各向异性值反射,提供有关尼元膜的界面域对小分子的界面域提供的温度诱导的变化的信息。温度依赖性荧光寿命研究证实了FT *的分布在两种不同位点的术语界面域,I。 e。缺水式内部部位和可散水外部部位。通过时间分辨荧光各向异性衰减进一步证实了FT *的这种异质性,得到了两种不同的旋转时间常数(B1.04 NS的更快成分来自可进入的外部部位,B16.50 NS的较慢组分起源于水 - 内部部位)。在TWEEN20中Fisetin的界面位置:胆固醇(1:1)定位膜具有关于从DPPH激进清除研究证实的抗氧化活性的重要意义。

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