The Structure and Surface Activity of Proteins in Surfactants and Surfactant Mixtures

2021 ◽  
Author(s):  
Jason Berberich ◽  
Kayla Thompson ◽  
Kerri Peterson ◽  
Evan Danielson ◽  
Jason Boock
2021 ◽  
Vol 9 ◽  
Author(s):  
Camillo La Mesa ◽  
Gianfranco Risuleo

The surface activity of surfactant mixtures is critically analyzed. Cat-anionic systems, in which two ionic species are mixed in non-stoichiometric ratios, are considered. With respect to the solution behavior, where a substantial decrease of cmc is met compared to the pure components, a moderate effect on surface tension, γ, occurs. Compared to the pure species, the decrease of surface tension for such mixtures is not significant, and no clear dependence on the mole fraction anionic/cationic is met. The surface tension is grossly constant in the whole concentration range. Conversely, the interaction parameter for surfaces, βsurf (calculated by the regular solution theory), is more negative than that for micelle formation, βmic. This fact suggests that the desolvation of polar heads of the two species at interfaces is largely different. Very presumably, the underlying rationale finds origin in the sizes and solvation of both polar head groups.


Author(s):  
E. Naranjo

Equilibrium vesicles, those which are the stable form of aggregation and form spontaneously on mixing surfactant with water, have never been demonstrated in single component bilayers and only rarely in lipid or surfactant mixtures. Designing a simple and general method for producing spontaneous and stable vesicles depends on a better understanding of the thermodynamics of aggregation, the interplay of intermolecular forces in surfactants, and an efficient way of doing structural characterization in dynamic systems.


2020 ◽  
Author(s):  
Zahari Vinarov ◽  
Gabriela Gancheva ◽  
Nikola Burdzhiev ◽  
Slavka S. Tcholakova

Although surfactants are frequently used in enabling formulations of poorly water-soluble drugs, the link between their structure and drug solubilization capacity is still unclear. We studied the solubilization of the “brick-dust” molecule itraconazole by 16 surfactants and 3 phospholipid:surfactant mixtures. NMR spectroscopy was used to study in more details the drug-surfactant interactions. Very high solubility of itraconazole (up to 3.6 g/L) was measured in anionic surfactant micelles at pH = 3, due to electrostatic attraction between the oppositely charged (at this pH) drug and surfactant molecules. <sup>1</sup>H NMR spectroscopy showed that itraconazole is ionized at two sites (2+ charge) at these conditions: in the phenoxy-linked piperazine nitrogen and in the dioxolane-linked triazole ring. The increase of amphiphile hydrophobic chain length had a markedly different effect, depending on the amphiphile type: the solubilization capacity of single-chain surfactants increased, whereas a decrease was observed for double-chained surfactants (phosphatidylglycerols). The excellent correlation between the chain melting temperatures of phosphatidylglycerols and itraconazole solubilization illustrated the importance of hydrophobic chain mobility. This study provides rules for selection of itraconazole solubilizers among classical single-chain surfactants and phospholipids. The basic physics underpinning the described effects suggests that these rules should be transferrable to other “brick-dust” molecules.


1993 ◽  
Vol 58 (3) ◽  
pp. 496-505
Author(s):  
Ondřej Wein

Partial blocking of the transport surface under the stagnant (nerst) layer is simulated by periodically alternating bands of perfectly insulating zones and active zones with a constant potential of driving force. The numeric solution of the corresponding two-dimensional elliptic problem is represented by a simple empirical correlation for the transfer coefficients. The result is interpreted in terms of a simple electrochemical problem about limiting diffusion currents at electrodes with non-uniform surface activity.


2021 ◽  
Vol 334 ◽  
pp. 115988
Author(s):  
Angelica Mero ◽  
Andrea Mezzetta ◽  
Janusz Nowicki ◽  
Justyna Łuczak ◽  
Lorenzo Guazzelli

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