分光光度法研究硝酸依伯康唑在胶束介质中的解离平衡

M. V. Krishna, S. A. Idris, G. Madhavi, B. J. Reddy, M. Sowhardhra, D. Sankar
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引用次数: 0

摘要

平衡解离常数(KD)是评价化合物化学结构结合性能的基本参数。因此,建立了多种分析方法来确定KD值,包括放射配基结合法、表面等离子体共振法、荧光能量共振转移法、亲和色谱法和等温滴定量热法。本文详细介绍了硝酸埃伯康唑(Eberconazole nitrate, EBZ)在均相和非均相体系中的解离平衡,重点介绍了基于分光光度法的解离反应方法。在布里顿-罗宾逊缓冲液(BR)中,用分光光度法研究了硝酸埃伯康唑(EBZ)在均相和非均相体系中的解离平衡。在BR缓冲液中发现EBZ的酸度常数为9.5。在超过临界胶束浓度(cmc)的条件下,考察了阴离子、阳离子和非离子表面活性剂对EBZ酸碱性能的影响。结果显示胶束介质中的pKa值与BR缓冲液中的值相比发生了变化。这些pKa值的变化在阳离子和阴离子胶束介质中比在非离子胶束介质中更明显。胶束介质与BR缓冲溶液的pKa值差异在-6.0 ~ -2.0单位之间。胶束介导的pKa位移可以归因于界面相和体相的平均固有溶剂性质之间的差异,在带电胶束水溶液的情况下,静电胶束表面电位也有额外的贡献。
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Study on Dissociation Equilibria of Eberconazole Nitrate in Micellar Media by Spectrophotometry
The equilibrium dissociation constant (KD) is the basic parameter to evaluate the binding property of the chemical structure of compounds. Thus, a variety of analytical methods have been established to determine the KD values, including radioligand binding assay, surface plasmon resonance method, fluorescence energy resonance transfer method, affinity chromatography, and isothermal titration calorimetry. Here we present a detailed overview of the dissociation equilibria of Eberconazole nitrate (EBZ) in homogeneous and heterogeneous systems, focusing primarily on methods that are based on spectrophotometrically of the dissociation reaction. The Dissociation equilibria of Eberconazole nitrate (EBZ) in homogeneous and heterogeneous systems were studied spectrophotometrically in Britton-Robinson’s (BR) buffer at 25°C. Acidity constant of EBZ in BR buffer was found to be 9.5. The effect of anionic, cationic and non-ionic surfactants applied in the concentration exceeding critical micellar concentration (cmc) on acid – base properties of EBZ were also examined. The results revealed a shift of pKa values in micellar media comparing to the values obtained in BR buffer. These shifts in pKa values are more in cationic and anionic micellar media compared with that of non-ionic. The observed differences in pKa values between micellar media and BR buffer solution ranged between -6.0 to -2.0 units. The micellar-mediated pKa shifts can be attributed to the differences between the mean intrinsic solvent properties of the interfacial and bulk phases, with an additional contribution from the electrostatic micellar surface potential in the case of the charged aqueous micellar solutions.
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