2010
DOI: 10.1016/j.colsurfb.2010.06.027
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Significant effect of polar head group of surfactants on the solubilization of Zein in mixed micellar (SDS–DDAB) media

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Cited by 21 publications
(15 citation statements)
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“…These cases can be explained by the formation of compact mixed micelle due to the intercalation of nonionic OP-10 at x 1 < 0.6 and the increase of electrostatic repulsion between the ionic headgroups of C12AS at x 1 > 0.6 [18]. The similar viewpoint can be supported by some previous investigations [19][20][21][22].…”
Section: Micellization Of C12as Op-10 and Their Mixtures In Aqueous supporting
confidence: 65%
“…These cases can be explained by the formation of compact mixed micelle due to the intercalation of nonionic OP-10 at x 1 < 0.6 and the increase of electrostatic repulsion between the ionic headgroups of C12AS at x 1 > 0.6 [18]. The similar viewpoint can be supported by some previous investigations [19][20][21][22].…”
Section: Micellization Of C12as Op-10 and Their Mixtures In Aqueous supporting
confidence: 65%
“…Several studies have been published on the determination of the CMC of surfactants using various methods [22][23][24][25][26][27][28]. But, there are a few reports on the determination of CMC for surfactants (anionic, cationic and non ionic) by UV spectroscopy [29].…”
Section: Introductionmentioning
confidence: 99%
“…Both of them are hydrophobic proteins. , Thus, zein is often employed as a model protein to evaluate the skin irritation potential of surfactants. Cationic surfactants bind with zein mainly by the hydrophobic interactions of their hydrocarbon chains with the hydrophobic domains of zein and the electrostatic attraction between their cationic headgroups and some negatively charged amino acid residues in zein . Therefore, reducing the number of hydrophobic chains and the charge density of cationic surfactant headgroups is favorable for improvement of the mildness of surfactants.…”
Section: Resultsmentioning
confidence: 99%
“…Cationic surfactants bind with zein mainly by the hydrophobic interactions of their hydrocarbon chains with the hydrophobic domains of zein and the electrostatic attraction between their cationic headgroups and some negatively charged amino acid residues in zein. 67 Therefore, reducing the number of hydrophobic chains and the charge density of cationic surfactant headgroups is favorable for improvement of the mildness of surfactants. In addition, recent studies also suggested that the surfactants with stronger self-assembling ability and larger aggregates show weaker skin irritation.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%