@article {4204,
	title = {Recent developments towards a unified theory for separation science},
	journal = {Electrophoresis},
	volume = {19},
	number = {10},
	year = {1998},
	note = {ISI Document Delivery No.: 108XDTimes Cited: 0Cited Reference Count: 30},
	month = {Jul},
	pages = {1586-1589},
	type = {Review},
	abstract = {Various techniques for chemical separation can be described using a generally applicable theory. There are several schools of thought on how a unified separation science should be developed. The theories described include the mass balance equation (i.e. moving boundary), virtual migration distances, and the use of individual capacity factors.},
	keywords = {CAPILLARIES, HIGH-PERFORMANCE ELECTROPHORESIS, individual capacity factors, INTERPLAY, LIQUID-CHROMATOGRAPHY, mass balance equation, resolution equation, separation science, virtual migration distances},
	isbn = {0173-0835},
	url = {<Go to ISI>://000075290300010},
	author = {Bowser, M. T. and Chen, D. D. Y.}
}
@article {4099,
	title = {Quantitative description of analyte migration behavior based on the dynamic complexation model in capillary electrophoresis},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {75},
	number = {5},
	year = {1997},
	note = {ISI Document Delivery No.: XF492Times Cited: 20Cited Reference Count: 27},
	month = {May},
	pages = {507-517},
	type = {Article},
	abstract = {A theory based on dynamic complexation is used to describe analyte migration behavior in capillary electrophoresis (CE). This theory is based on a one-phase system, instead of the commonly accepted two-phase system. The migration behavior of an analyte is described by three parameters (the electrophoretic mobility of the free analyte, the electrophoretic mobility of the analyte-additive complex, and the equilibrium constant (formation constant) that determines the fractions of the free analyte and the complex at a certain additive concentration). Varying the additive concentration shifts the equilibrium and changes the viscosity of the background electrolyte. Viscosity correction is crucial in interpreting the observed migration behavior of analytes. While electroosmotic flow in a capillary often varies from one capillary to another, the viscosity of a buffer is characteristic of the buffer composition and is constant for each buffer. The electrophoretic mobility of a certain species and the equilibrium constant are intrinsic properties and are less sensitive to changes in the environment. Understanding these relationships is indispensable in CE method development and method validation. A universal resolution equation is proposed, with a separation factor that has taken both the electrophoretic mobilities and equilibria into consideration. This resolution equation gives clear guidance for the optimization of CE separations. A group of nucleosides and their phosphates are used as analytes, and P-cyclodextrin is used as the additive in the model system studied in this paper. Both the observed analyte migration behavior and the resolution of analytes agree well with this theory.},
	keywords = {ACIDS, BETA-CYCLODEXTRIN, BINDING, capacity factor, CHIRAL SEPARATION, CORRECTION, dynamic complexation capillary electrophoresis, ELECTROKINETIC CHROMATOGRAPHY, mobility, nucleoside and, nucleotide separation, RESOLUTION, resolution equation, VISCOSITY},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1997XF49200005},
	author = {Peng, X. J. and Bebault, G. M. and Sacks, S. L. and Chen, D. D. Y.}
}
