Department of Chemistry, Indian Institute of Technology, Kharagpur 721302, WB, India.
J Phys Chem B. 2012 Aug 2;116(30):8780-92. doi: 10.1021/jp302435h. Epub 2012 Jul 6.
The modulation of the photophysical properties of 1'-hydroxy-2'-acetonaphthone (HAN) upon encapsulation into the hydrophobic nanocavities of different bile salt aggregates has been investigated for the first time using steady-state and time-resolved fluorescence spectroscopy. Because HAN is very sensitive to the polarity of the microenvironment in which it is confined, we performed a comparative study on the excited-state binding dynamics of HAN using three different bile salts of varying hydrophobicity. The encapsulation of HAN into the bile salt aggregates led to an enhanced fluorescence intensity along with a significant blue shift in the emission maxima that was highly sensitive to the confined microenvironment. Using HAN as a sensitive fluorophore to probe the nanocavities of bile salt aggregates in aqueous solution, we found different mechanisms of probe encapsulation depending on the degree of hydrophobicity of the nanocavities, which results in a difference in the alteration of the spectral behavior. A sharp increase in the fluorescence quantum yield near the cmc was observed, followed by saturation for all three bile salt aggregates. However, maximum fluorescence quantum yield in NaDC aggregates can be rationalized by maximum partitioning of HAN into the more hydrophobic and rigid environment provided by NaDC aggregates. Moreover, the alteration of the spectral behavior with increasing concentration of bile salts strikingly differs from that observed previously in the presence of conventional surfactants. Time-resolved fluorescence measurements further elucidated how the probe molecules interact with the aggregates. Longer fluorescence lifetime and anisotropy values clearly indicate the caging of the tautomers of HAN into the hydrophobic nanocavities of bile salt aggregates. This work further demonstrates the changes in the fluorescence properties of HAN with structural changes of bile salt aggregates induced by the addition of salt and organic cosolvent.
首次使用稳态和时间分辨荧光光谱法研究了 1'-羟基-2'-乙酰萘(HAN)在包封到不同胆盐聚集体的疏水性纳米腔中时其光物理性质的调制。由于 HAN 对其被限制的微环境的极性非常敏感,我们使用三种不同疏水性的胆盐进行了 HAN 激发态结合动力学的比较研究。HAN 被包封到胆盐聚集体中会导致荧光强度增强,同时发射最大值发生显著蓝移,这对受限的微环境非常敏感。使用 HAN 作为灵敏荧光探针来探测水溶液中胆盐聚集体的纳米腔,我们发现了根据纳米腔的疏水性程度不同的探针包封机制,这导致光谱行为的变化不同。在 cmc 附近观察到荧光量子产率的急剧增加,随后所有三种胆盐聚集体的荧光量子产率都达到饱和。然而,NaDC 聚集体中最大的荧光量子产率可以通过 HAN 最大地分配到由 NaDC 聚集体提供的更疏水和刚性的环境来合理化。此外,随着胆盐浓度的增加,光谱行为的变化与以前在存在常规表面活性剂时观察到的明显不同。时间分辨荧光测量进一步阐明了探针分子如何与聚集体相互作用。更长的荧光寿命和各向异性值清楚地表明,HAN 的互变异构体被笼封到胆盐聚集体的疏水性纳米腔中。这项工作进一步证明了随着盐和有机溶剂的添加引起的胆盐聚集体结构变化,HAN 的荧光性质发生了变化。