Synergism and formation of vesicle gels in salt-free catanionic hydrocarbon/fluorocarbon surfactant mixtures

RSC Advances ◽  
2014 ◽  
Vol 4 (76) ◽  
pp. 40595-40605 ◽  
Author(s):  
Mei Yang ◽  
Jingcheng Hao ◽  
Hongguang Li
1992 ◽  
Vol 45 (4) ◽  
pp. 769 ◽  
Author(s):  
TJ Connolly ◽  
VC Reinsborough ◽  
XY Xiang

Solubilities of pyridine-2-azo-p-dimethylaniline ( pada ) were determined at 25�C in four mixed fluorocarbon/hydrocarbon short-chained surfactant systems: ( i ) sodium decyl sulfate/sodium perfluoroheptanoate; (ii) sodium octanesulfonate /sodium perfluorooctanoate ; (iii) sodium octanesulfonate /sodium perfluoroheptanoate ; (iv) sodium nonanesulfonate /sodium perfluoroheptanoate. Systems ( i ), (iii) and (iv) showed micellar miscibility (one mixed micelle) and synergistic solubilization effects. System (ii) had two critical micelle concentrations pointing to two micellar forms in solution, and no synergism could be detected. From these four examples, it is deduced that single mixed micelles are formed when the critical micelle concentrations of the pure surfactants are within a factor of 3 of each other.


2006 ◽  
Vol 110 (23) ◽  
pp. 11369-11376 ◽  
Author(s):  
Elena Blanco ◽  
Paula Messina ◽  
Juan M. Ruso ◽  
Gerardo Prieto ◽  
Félix Sarmiento

2014 ◽  
Vol 417 ◽  
pp. 180-187 ◽  
Author(s):  
Katarzyna Szymczyk ◽  
Maria Luisa González-Martín ◽  
Jose Morales Bruque ◽  
Bronisław Jańczuk

2021 ◽  
Vol 3 (1) ◽  
Author(s):  
Yutang Zhou ◽  
Yong Jin ◽  
Yichao Shen ◽  
Liangjie Shi ◽  
Shuangquan Lai ◽  
...  

Abstract Mixing hydrocarbon surfactants with fluorocarbon surfactants is still an important strategy to improve the economic benefits and performances of fluorocarbon surfactants and expand their range of application. Herein, we prepared a novel kind of hydrocarbon-fluorocarbon surfactant mixtures via mixing a cationic surfactant, cetyltrimethylammonium bromide (CTAB), with a tri-block nonionic short-chain fluorocarbon surfactant (F9EG13F9) in aqueous solution. The results showed that adding a small CTAB amount to F9EG13F9 (the molar fraction of CTAB in the mixture (x1) was 0.2) could greatly reduce its critical micelle concentrations (cmc) from 0.408 mmol/L to 0.191 mmol/L. At this x1, the contact angle of the mixture was the minimum (57.7 °) at 100 s on polytetrafluoroethylene film, which was even lower than that of F9EG13F9. Besides, CTAB/F9EG13F9 mixtures possessed better colloidal stability and solubilization ability toward hydrophobic dye (Sudan І) than F9EG13F9. The outstanding performances of binary surfactant mixtures benefited from the non-ideal mixing and strong synergistic effect evidence that CTAB/F9EG13F9 surfactant mixtures could be used in practical applications instead of individual F9EG13F9, thereby reducing the used cost of F9EG13F9. Graphical abstract


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.


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