Formation of oil-in-water nano-emulsions has been studied in the water/C12E4/isohexadecane system by the phase inversion temperature emulsification method. Emulsification started at the corresponding hydrophilic-lipophilic balance temperature, and then the samples were quickly cooled to 25 degrees C. The influence of phase behavior on nano-emulsion droplet size and stability has been studied. Droplet size was determined by dynamic light scattering, and nano-emulsion stability was assessed, measuring the variation of droplet size as a function of time. The results obtained showed that the smallest droplet sizes were produced in samples where the emulsification started in a bicontinuous microemulsion (D) phase region or in a two-phase region consisting of a microemulsion (D) and a liquid crystalline phase (L(alpha)). Although the breakdown process of nano-emulsions could be attributed to the oil transference from the smaller to the bigger droplets, the increase in instability found with the increase in surfactant concentration may be related to the higher surfactant excess, favoring the oil micellar transport between the emulsion droplets.
A kinetic model describing the fluorescence quenching of micelle-solubilized probes including intermicellar quencher exchange is tested in detail with pyrene and pyrene derivatives as fluorescent probes, 10 metal ions as quenchers, and SDS as soap. The rate constants obtained are discussed, with emphasis on kqm, the micellar quenching rate constant. An empirical model and a theoretical model for the first-order micellar quenching rate constant are compared; both lead to excellent agreement with the experimental observations.
Active ingredients have been around in cosmetics for a long time but have they really resulted in active cosmetic products? In order to achieve this, the right active needs to be delivered to the right location at the right concentration for the correct period of time. And the extent (and therefore the concentration) of this delivery depends on the formulation. From a rather theoretical approach based on the polarity of the active ingredient, the stratum corneum and the oil phase, the Relative Polarity Index was established that enables the selection of a suitable emollient for ensuring skin penetration of the active ingredient. Practical examples subsequently show the validity of this approach that demonstrates that one can regulate the delivery of an active molecule (and therefore the efficacy of a cosmetic formulation) by selection and control of the emollient system. Cosmetic formulations are generally quite complex mixtures and subsequent experiments using different emulsifier systems indicated that this component of a cosmetic formulation could also have an impact on steering the active ingredient to the right layer of the skin, although it is too early to be able to derive general rules from this.
Articles you may be interested inRate kernel theory for pseudo-first-order kinetics of diffusion-influenced reactions and application to fluorescence quenching kinetics Fluorescence quenching by reversible excitation transfer: Application of a hierarchy approach to a pseudo firstorder modelConsidering the fact that in a micellar medium solubilized molecules are mostly present near the surface, a solution of Fick's diffusion law on a spherical surface is obtained to calculate the rate of diffusion controlled reactions in a micelle. It is shown that transients are small. Corrections are applied for the radial distribution of probe and quencher. The model is extended to reactions slower than diffusion controlled.
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