1. Study on Dissociation Equilibria of Eberconazole Nitrate in Micellar Media by Spectrophotometry
- Author
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D. Gowri Sankar, Marothu Vamsi Krishna, M. Sowhardhra, B. Jalachandra Reddy, Gajulapalle Madhavi, and Salah Ali Mahgoub Idris
- Subjects
Dissociation constant ,chemistry.chemical_compound ,Aqueous solution ,chemistry ,Critical micelle concentration ,Micellar solutions ,Inorganic chemistry ,technology, industry, and agriculture ,Buffer solution ,Acid dissociation constant ,Eberconazole ,Dissociation (chemistry) - Abstract
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.
- Published
- 2019
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