Surfactants And The Stratum Corneum Lipids

A simplified mixture of model stratum corneum lipids was mixed with different surfactants to make a preliminary estimation of the influence of surfactants on the stratum corneum lipid structure. The results revealed differences between cationic and anionic surfactants and between anionic surfactants with different structures. © 1998

Formation and dissolution of surfactant precipitates.

Precipitation of surfactants is one of the most important considerations in surfactant applications. Understanding the formation and dissolution of surfactant precipitates provides more effective utilization of surfactants. In this study, firstly, the kinetics of precipitation of mixed anionic surfactants with calcium ion was studied and the relationship between the supersaturation ratios of precipitating surfactants and the rate of surfactant precipitation was established. The precipitation in mixed anionic surfactants is delayed substantially when the supersaturation ratios of precipitating surfactants are approximately the same, indicating the growth of each precipitating surfactant is interrupted by use of growing crystals as nucleation sites for the dissimilar surfactant to form crystals. Secondly, precipitation phase boundaries of an anionic surfactant and a pH sensitive amphoteric surfactant were measured and modeled at different pH levels. A hydrogen ion titration to obtain the pKa of the amphoteric surfactant, regular solution theory to describe mixed micelle formation, and the solubility product of the precipitate were combined to predict the precipitation phase boundary. Lastly, the thermodynamics and kinetics of the dissolution of precipitate of calcium salt of a long chain fatty acid or soap scum using water-soluble surfactants and ligand were studied. Simultaneous removal of calcium from the soap scum molecule by ligand complexation and formation of mixed micelles of the alkyl carboxylate anion molecules and co-surfactants are responsible for high solubility and rapid dissolution of soap scum. The solution pH plays an important role in the dissolution in this system as pH affects the dissociation of calcium from soap scum molecule and the release of calcium by affecting the effectiveness of the chelating agent used, as well as affecting the formation of mixed micelles by altering the charge on the surfactant head groups of a pH-sensitive amphoteric surfactant when used as an added surfactant

Mixed adsorption and surface tension prediction of nonideal ternary surfactant systems

To deal with the mixed adsorption of nonideal ternary surfactant systems, the regular solution approximation for nonideal binary surfactant systems is extended and a pseudo-binary system treatment is also proposed. With both treatments, the compositions of the mixed monolayer and the solution concentrations required to produce given surface tensions can be predicted based only on the gamma-LogC curves of individual surfactants and the pair interaction parameters. Conversely, the surface tensions of solutions with different bulk compositions can be predicted by the surface tension equations for mixed surfactant systems. Two ternary systems: SDS/Hyamine 1622/AEO7, composed of homogeneous surfactants, and AES/DPCl/AEO9, composed of commercial surfactants, in the presence of excess NaCl, are examined for the applicability of the two treatments. The results show that, in general, the pseudo-binary system treatment gives better prediction than the extended regular solution approximation, and the applicability of the latter to typical anionic/cationic/nonionic nonideal ternary surfactant systems seems to depend on the combined interaction parameter, $${\mathop {(\beta }\nolimits_{an}^s } + {\mathop \beta \nolimits_{cn}^s })/2 - {\mathop \beta \nolimits_{ac}^s }/4$$ : the more it deviates from zero, the larger the prediction difference. If $${\mathop {(\beta }\nolimits_{an}^s } + {\mathop \beta \nolimits_{cn}^s })/2 - {\mathop \beta \nolimits_{ac}^s }/4$$ rarr0, good agreements between predicted and experimental results can be obtained and both treatments, though differently derived, are interrelated and tend to be equivalent

Efektivitas Ukuran Blok Campuran Tanah dan Hydraulic Loading Rate Pada Multi Soil Layering Guna Menurunkan Parameter Fosfat dan Surfaktan Anionik di Usaha Binatu

The laundry business is one of the business that produces phosphate and anionic surfactant parameters that cause eutrophication and environmental pollution. Parameters of phosphate and anionic surfactants can be reduced using multi soil layering with two stages. This study aims to analyze the effect of soil mixed block size and hydraulic loading rate on reducing pollutant concentration. The materials used in this study are andosol soil, rice husk charcoal and iron powder. The permeable layer uses gravel and pearlite media. The reactor is made of acrylic with a length of 50 cm, a width of 15 cm and a height of 50 cm. Multi soil layering systems successfully reduce concentrations to 98,603% for phosphate parameters and 99.99% for anionic surfactant parameters. The decrease in phosphate parameters and anionic surfactants is caused by physical and chemical adsorption processes by soil components and rice husk charcoal. The decrease in the parameters of anionic surfactants is also helped by the process of biodegradation of microbes in the soil

Weak and saturable protein-surfactant interactions in the denaturation of apo-α-lactalbumin by acidic and lactonic sophorolipid

Biosurfactants are of growing interest as sustainable alternatives to fossil-fuel-derived chemical surfactants, particularly for the detergent industry. To realize this potential, it is necessary to understand how they affect proteins which they may encounter in their applications. However, knowledge of such interactions is limited. Here, we present a study of the interactions between the model protein apo-alpha-lactalbumin (apo-aLA) and the biosurfactant sophorolipid (SL) produced by the yeast Starmerella bombicola. SL occurs both as an acidic and a lactonic form; the lactonic form (lactSL) is sparingly soluble and has a lower critical micelle concentration (cmc) than the acidic form [non-acetylated acidic sophorolipid (acidSL)]. We show that acidSL affects apo-aLA in a similar way to the related glycolipid biosurfactant rhamnolipid (RL), with the important difference that RL is also active below the cmc in contrast to acidSL. Using isothermal titration calorimetry data, we show that acidSL has weak and saturable interactions with apo-aLA at low concentrations; due to the relatively low cmc of acidSL (which means that the monomer concentration is limited to ca. 0-1 mM SL), it is only possible to observe interactions with monomeric acidSL at high apo-aLA concentrations. However, the denaturation kinetics of apo-aLA in the presence of acidSL are consistent with a collaboration between monomeric and micellar surfactant species, similar to RL and non-ionic or zwitterionic surfactants. Inclusion of diacetylated lactonic sophorolipid (lactSL) as mixed micelles with acidSL lowers the cmc and this effectively reduces the rate of unfolding, emphasizing that SL like other biosurfactants is a gentle anionic surfactant. Our data highlight the potential of these biosurfactants for future use in the detergent and pharmaceutical industry

Effect of surfactants on liquid side mass transfer coefficients

In the present paper, the effect of liquid properties (surfactants) on bubble generation phenomenon, interfacial area and liquid side mass transfer coefficient was investigated. The measurements of surface tension (static and dynamic methods), of Critical Micelle Concentration (CMC) and of characteristic adsorption parameters such as the surface coverage ratio at equilibrium (se) were performed to understand the effects of surfactants on the mass transfer efficiency. Tap water and aqueous solutions with surfactants (cationic and anionic) were used as liquid phases and an elastic membrane with a single orifice as gas sparger. The bubbles were generated into a small-scale bubble column. The local liquid side mass transfer coefficient (kL) was obtained from the volumetric mass transfer coefficient (kLa) and the interfacial area (a) was deduced from the bubble diameter (DB), the bubble frequency (fB) and the terminal bubble rising velocity (UB). Only the dynamic bubble regime was considered in this work (ReOR = 150 - 1000 and We = 0.002 - 4). This study has clearly shown that the presence of surfactants affects the bubble generation phenomenon and thus the interfacial area (a) and the different mass transfer parameters, such as the volumetric mass transfer coefficient (kLa) and the liquid-side mass transfer coefficient (kL). Whatever the operating conditions, the new kLa determination method has provided good accuracy without assuming that the liquid phase is perfectly mixed as in the classical method. The surface coverage ratio (se) proves to be crucial for predicting the changes of kL in aqueous solutions with surfactants

The removal of thermally aged films of triacylglycerides by surfactant solutions

Thermal ageing of triacylglycerides (TAG) at high temperatures produces films which resist removal using aqueous surfactant solutions. We used a mass loss method to investigate the removal of thermally aged TAG films from hard surfaces using aqueous solutions of surfactants of different charge types. It was found that cationic surfactants are most effective at high pH, whereas anionics are most effective at low pH and a non-ionic surfactant is most effective at intermediate pH. We showed that the TAG film removal process occurs in several stages. In the first ‘‘lag phase’’ no TAG removal occurs; the surfactant first partitions into the thermally aged film. In the second stage, the TAG film containing surfactant was removed by solubilisation into micelles in the aqueous solution. The effects of pH and surfactant charge on the TAG removal process correlate with the effects of these variables on the extent of surfactant partitioning to the TAG film and on the maximum extent of TAG solubilisation within the micelles. Additionally, we showed how the TAG removal is enhanced by the addition of amphiphilic additives such as alcohols which act as co-surfactants. The study demonstrates that aqueous surfactant solutions provide a viable and more benign alternative to current methods for the removal of thermally aged TAG films

The influence of natural pulmonary surfactant on the efficacy of siRNA-loaded dextran nanogels

Aim: Topical administration of siRNA nanocarriers is a promising approach in the treatment of pulmonary disorders. Pulmonary surfactant, covering the entire alveolar surface of mammalian lungs, will be one of the first interfaces that siRNA nanocarriers encounter upon inhalation therapy. Therefore, it is of outstanding importance to evaluate the impact of pulmonary surfactant on the performance of siRNA nanocarriers. Materials & methods: The effect of natural lung-derived surfactants on the siRNA delivery capacity of dextran nanogels (DEX-NGs) was evaluated in vitro using flow cytometry and confocal microscopy. Results: Although the interaction with pulmonary surfactant decreases the cellular internalization of siRNA-loaded DEX-NGs significantly, the gene silencing potential of siRNA-loaded DEX-NGs was maintained. On the other hand, cationic lipid-based siRNA nanocarriers (Lipofectamine (TM) RNAiMAX) were incompatible with pulmonary surfactants. Conclusion: Our data suggest that pulmonary surfactant can enhance the intracellular siRNA delivery by DEX-NGs, thereby possibly providing new therapeutic opportunities