No abstract

The microenvironment of water droplets of sodium bis (2‐ethylhexyl) sulfosuccinate (AOT) and sodium cholate mixed reverse microemulsions was studied. Structural changes of water pockets in mixed reverse micelles were investigated by IR spectroscopy. The O‐H stretching vibrational absorption spectra in the region of 3000–3800 cm−1 were fit to three subpeaks with the Monte Carlo method. It was revealed that additives of sodium cholate suppress free water fraction in the water droplets of reverse micelles from 31% to 20% and support rising of bound fraction from 53% to 65%. The binding of optical probe ortho‐nitroaniline to the mixed reverse micelles was determined by UV–visible spectroscopy. It was found that introducing of additives of sodium cholate below its critical micelle concentration (CMC) causes increasing of values of binding constant Kb twice compared with reverse micelles modified with pure water. However, values of the binding constant were reduced 4‐fold at concentrations of sodium cholate higher than its CMC. Electrical conductivity of the reverse mixed micellar solutions (AOT + sodium cholate) was measured. Water‐induced percolation in conductance of mixed reverse microemulsions occurs at a lower value of water/surfactant molar ratio (W) under the influence of sodium cholate, viz. electrical percolation threshold decreases from W = 32 to W = 15. The size of water droplets was estimated with the dynamic light scattering method. It was found that additives of sodium cholate below and higher than the CMC results in increasing and decreasing of hydrodynamic diameters of the water droplets, respectively, but sizes of water droplets decrease at concentrations of sodium cholate higher than its CMC.

No abstract

No abstract

The interaction of surface-active drugs with surfactants, used in the simulation of artificial membranes by direct and reversed micelles, mainly determines the transport of drugs in the body and the complex process of the binding to receptors. Besides, the delivery of drugs into the body via microemulsions has been successfully used to reduce the first-pass metabolism. The structure of mixed reverse microemulsions based on the ionic surfactant sodium bis(2-ethylhexyl)sulfosuccinate (AOT) and the cationic surface active drug promethazine hydrochloride (PMT) was studied spectroscopically in the infrared and UV-visible regions, as well as using electrical conductivity and dynamic light scattering. The release profile of PMT from AOT-based microemulsions was studied using cellulose dialysis bags. The introduction of PMT additive into the water pockets of reverse AOT micelles leads to: a) an increase in free water fraction and a decrease in bound water fraction; b) changing the chromatographic retention factors of the model compounds; c) insignificant influence on the values of the binding constant of optical probe o-nitroaniline with the head groups of AOT; d) quenching of water-induced percolation in electrical conductance of reverse AOT microemulsions; e) a slight decrease in the size of water droplets at the same values of the molar ratio of water/surfactant. The release of PMT from the aqueous system obeys Fick’s law of diffusion (n = 0.4852), and the release of PMT from microemulsions is based on non-Fickian or anomalous diffusion.