Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0021-9673(02)01823-X
Title: Indirect capillary electrophoresis with 8-anilino-1-naphthalenesulfonic acid as a fluorescence probe for determining the apparent stability constant of an inclusion complex formed between a cyclodextrin and a solute
Authors: Wang, T.
Feng, H.
Li, S.F.Y. 
Keywords: Amantadine
Anilinonaphthalenesulfonic acid
Complexation
Cyclodextrins
Stability constants
Issue Date: 14-Feb-2003
Citation: Wang, T., Feng, H., Li, S.F.Y. (2003-02-14). Indirect capillary electrophoresis with 8-anilino-1-naphthalenesulfonic acid as a fluorescence probe for determining the apparent stability constant of an inclusion complex formed between a cyclodextrin and a solute. Journal of Chromatography A 987 (1-2) : 485-492. ScholarBank@NUS Repository. https://doi.org/10.1016/S0021-9673(02)01823-X
Abstract: An indirect capillary electrophoresis (CE) method was developed based on two competitive chemical equilibria for determining the stability constant of an inclusion complex formed between a cyclodextrin and a solute. 8-Anilino-1-naphthalenesulfonic acid was employed as a fluorescence probe. A linear relationship between mobility difference and concentration of uncomplexed ligand was theoretically established and experimentally verified. The principle of the method was explained using an example of determining stability constant of an inclusion complex formed between a ligand of hydroxypropyl-β-cyclodextrin and a solute of amantadine. The stability constant was determined to be ∼2·102 M-1. It was calculated without knowledge of the mobility of the complex measured at saturating ligand concentrations. This indirect method can be applied to solutes and ligands lacking signal response on the selected detector in the CE. In addition, the indirect method is valid for both charged and neutral solutes and ligands. © 2002 Elsevier Science B.V. All rights reserved.
Source Title: Journal of Chromatography A
URI: http://scholarbank.nus.edu.sg/handle/10635/95472
ISSN: 00219673
DOI: 10.1016/S0021-9673(02)01823-X
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