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  • Analytical Chemistry and Spectroscopy  (2)
  • Zone electrophoresis  (2)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 2 (1990), S. 229-233 
    ISSN: 1040-7685
    Keywords: capillary isotachophoresis ; capillary zone electrophoresis ; detectability enhancement ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple isotachophoretic (ITP) preconcentration column for subsequent online capillary zone electrophoresis is described, and its use for enhancing detectability in capillary zone electrophoresis (CZE) is evaluated. Sample preconcentration using ITP is shown to enhance detectability in CZE by several orders of magnitude. Experimental verification of the detectability gain is demonstrated for cationic and anionic separations; an increase in detectability of more than 200-fold was achieved. The practical applicability of this method is demonstrated using a direct analysis of thiamine in human blood.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 2 (1990), S. 80-83 
    ISSN: 1040-7685
    Keywords: capillary isotachophoresis ; determination of pyruvate ; acetoacetate ; 3-hydroxybutyrate ; lactate ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An isotachophoretic method was developed and optimized for simultaneous determination of pyruvate, acetoacetate, lactate, and 3-hydroxybutyrate in 1-10 μL of untreated heparin plasma of patients with diabetes mellitus. A commercial instrument with a column switching system was used. The preseparation capillary was filled with the leading electrolyte of pH 4.2 and the analytical capillary was filled with leading electrolyte of pH 3.0. The concentrations of individual ketone bodies and lactate found in human plasma varied within 0.01-1.4 mmol/L and 0.8-11.8 mmol/L, respectively. Analysis time was about 30 min.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 16 (1995), S. 1999-2007 
    ISSN: 0173-0835
    Keywords: Isotachophoresis ; Zone electrophoresis ; Separation theory ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: The qualitative characteristics of isotachophoresis differ substantially from “classical” separation methods such as chromatography or zone electrophoresis. Self-sharpening zone boundaries and step-like concentration profiles are the most specific features of this method, which does not allow the description of the isotachophoretic separation in usual “chromatographic” terms, such as resolution or number of theoretical plates. A theory is presented in this paper, combining the usual isotachophoretic separation characteristics with the theory of isotachophoretic zone boundary, which is the only element of the isotachophoretic system with dispersional properties. This allows us to consider situations near the limits of the isotachophoretic method as far as both selectivity and sample amount (i.e., zone size) are concerned. Based on a simplified expression of the concentration profiles across the isotachophoretic zone boundary, separation and separation limits are described and discussed in terms of resolution, selectivity and zone capacity. Equations are derived showing the relationships between resolution, boundary width, selectivity, sample amount, and column and electrolyte conditions. A simple phenomenological equation is presented, expressing isotachophoretic resolution as a function of only sample amount (or sample zone length) and boundary width. A thermo-dynamic form of this equation is derived, which is shown to be similar to such an expression for resolution in zone electrophoresis. In both cases resolution is a function of sample selectivity, electric field strength and column length. A simple theoretical model for zone capacity is presented, making it possible to estimate the separation performance of isotachophoretic systems. Based on the presented theory, parallels between isotachophoresis and zone electrophoresis are discussed and both methods are compared.
    Additional Material: 8 Ill.
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  • 4
    ISSN: 0173-0835
    Keywords: Zone electrophoresis ; Sample stacking ; Sample self-stacking ; Matrix effects ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A theoretical study is presented of zone electrophoretic behavior of samples that contain one or more minor analytes and at least one major ionogenic component of like charge. Based on a simple model comprising weak univalent anionic electrolytes, conditions are derived under which analytes are temporarily focused isotachophoretically into very narrow zones by a sample self-stacking effect provided by the major sample components. Requirements for minimal/maximal mobility and a background coion concentration dependent minimal concentration of a major sample component (stacker) are presented. For systems in which sample self-stacking does not apply, an expression for the concentrating factor is derived that involves the effects of both nonselective (classical) and selective sample stacking, the latter being a consequence of electrophoretic separation of the minor analyte from the major component. The theory derived is discussed with selected model examples by using both numerical calculation and computer simulation.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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