Interactions between β-cyclodextrin and an amino acid-based anionic gemini surfactant derived from cysteine

被引:22
|
作者
Faustino, Celia M. C. [1 ]
Calado, Antonio R. T. [1 ]
Garcia-Rio, Luis [2 ]
机构
[1] Univ Lisbon, Fac Pharm, iMed UL, P-1649003 Lisbon, Portugal
[2] Univ Santiago de Compostela, Fac Chem, Dept Phys Chem, Santiago De Compostela 15706, Spain
关键词
Amino acids; Complexation constant; Cyclodextrins; Cysteine; Gemini surfactants; Inclusion complexes; CRITICAL MICELLE CONCENTRATION; SODIUM DODECYL-SULFATE; SPECTRAL DISPLACEMENT; INCLUSION COMPLEXES; BINDING CONSTANTS; AQUEOUS-SOLUTION; WATER; NMR; ASSOCIATION; H-1-NMR;
D O I
10.1016/j.jcis.2011.07.101
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The interaction between beta-cyclodextrin (beta-CD) and an amino acid-based anionic gemini surfactant derived from cysteine (C(8)Cys)2 was studied by three independent techniques: electrical conductivity, UV-Vis spectral displacement technique using phenolphthalein as probe, and H-1 NMR spectroscopy. The data obtained indicated the formation of a 1:1 inclusion complex between beta-CD and the gemini surfactant studied and allowed for the determination of the binding constant, K-1, by considering this stoichiometry. Electrical conductivity, spectral displacement technique, and NMR chemical shift measurements, obtained for aqueous beta-CD-surfactant systems, yielded consistent K-1 values in the order of 10(2) dm(3) mol(-1), typical of a weakly bound beta-CD-surfactant complex. The influence of the presence of the inclusion complex on the micellization process of the gemini surfactant has also been studied and the apparent critical micelle concentration (cmc*) has been obtained. Increasing beta-CD concentration was found to shift the cmc* to higher values, as complexed surfactant monomers are not available to form micelles and aggregation takes place only when all beta-CD cavities are occupied. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:286 / 292
页数:7
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