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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 3 (1991), S. 141-145 
    ISSN: 1040-7685
    Keywords: capillary electrophoresis ; copper electrode detection ; amino acids ; catecholamines ; peptides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The use of a copper wire amperometric detector for capillary electrophoresis is reported. Detection is accomplished by use of a porous glass joint, which allows amperometric detection at a copper wire electrode inserted in the end of the capillary. An anodic current is produced by a change in the copper oxide film solubility, resulting from complexation of copper ions with certain analytes at the electrode surface. This copper/copper oxide electrode has been used to detect nonelectroactive native amino acids and dipeptides. Subfemtomole detection limits in picoliter injection volumes have been obtained without solute derivatization. In addition, simultaneous analysis of nonelectroactive amino acids and electroactive catecholamines has been demonstrated.
    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 6 (1994), S. 97-106 
    ISSN: 1040-7685
    Keywords: electrogenerated chemiluminescence ; luminol ; capillary electrophoresis ; microelectrodes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrogenerated chemiluminescence (ECL) detection based on the reaction of luminol and H2O2 has been developed for capillary electrophoresis. The ECL response at carbon fiber and platinum wire microelectrodes has been investigated. Carbon fiber electrodes are observed to be less sensitive than platinum electrodes but provide a more stable response. The ECL response at a carbon fiber electrode is linear over three orders of magnitude for luminol with a linear correlation coefficient of 0.998. Mass detection limits of 92 amol and 260 amol have been obtained for luminol using platinum wire microelectrodes and carbon fiber microelectrodes, respectively. The influence of hydrogen peroxide concentration (in the detection buffer resrvoir) on the luminescence response has been examined and found to be dependent on electrode type. The dependence of the ECL response on the applied voltage at the microelectrode has been studied for both electrode types. Capillary electrophoresis with ECL detection has been used for analysis of amines derivatized with N-(4-aminobutyl)-N-ethylisoluminol coupled to N, N-disuccinimidylcarbonate (ABEI-DSC). Detection limits of 2.0 fmol and 0.96 fmol are obtained for n-octylamine and n-propylamine, respectively. In addition, ABEI-DSC has been used to successfully label the tripeptide Val-Tyr-Val, and micellar electrokinetic capillary chromatography has been used with ECL detection for the separation of ABEI-DSC labeled amines.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 6 (1994), S. 373-384 
    ISSN: 1040-7685
    Keywords: capillary electrophoresis ; post-column derivatization ; fluorescence ; OPA ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The construction and performance of a post-column reactor for capillary electrophoresis with laser-induced fluorescence detection in 10 μm i.d. capillaries is described. The post-column reactor is based on a gap design and relies primarily on diffusion for addition and mixing of derivatizing reagents. Reactors with gaps of 4 to 160 μm are easily built with minimal micromanipulation between two 10 μm i.d. capillaries. Optimal separation efficiencies and sensitivities are obtained with gaps of less than 10 μm. Separations of amino acids and proteins with o-phthaldialdehyde/2-mercaptoethanol post-column derivatization and laser-induced fluorescence detection are shown. Linear detector response is found for amino acids and proteins, and peak efficiencies as high as 230,000 theoretical plates are obtained for some analytes. The use of relatively small columns for capillary electrophoresis results in a separation and detection system that produces very low mass detection limits for biological molecules from picoliter sample injections. Mass detection limits of 130 and 5.2 attomoles are obtained for glycine and human transferrin, respectively.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 6 (1994), S. 263-268 
    ISSN: 1040-7685
    Keywords: capillary electrophoresis ; scanning electrochemical detection ; voltammetric detection ; catecholamines ; peptides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Scanning electrochemical detection has been combined with capillary electrophoresis to increase the resolving power for closely eluting solutes. This detection mode has been characterized and provides voltammetric information for easily oxidized solutes with linear detection over concentrations in the 10-3 to 10-5 M range. Detection limits for catechols range from 360 amol to 740 amol (2.3 μM to 6.6 μM concentrations). Finally, two neutral solutes, catechol and tryptophan, co-elute under zone electrophoresis conditions, but are resolved with scanning detection.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 2 (1990), S. 176-180 
    ISSN: 1040-7685
    Keywords: electroosmosis ; buffer effects ; capillary electrophoresis ; alcohol effects ; ionic strength ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Solute migration in capillary electrophoresis is the sum of the molecularly specific electrophoretic mobility and the electric-field-induced solvent flow (electroosmosis). This solvent flow is an important component of capillary electrophoresis and has been linked to resolution and automation aspects of this technique. This work demonstrates that equivalent electroosmotic flows can be achieved using different buffer types if the ionic strength is equal in the two systems. The effects of the addition of acetonitrile and several different alcohols on electroosmotic flow are also examined. The data suggest a unique surface effect of alcohols on the observed electroosmotic flow.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 6 (1994), S. 483-494 
    ISSN: 1040-7685
    Keywords: continuous electrophoresis ; channel electrophoresis ; capillary electrophoresis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Continuous electrophoretic separations in narrow channels have been carried out by coupling conventional capillary zone electrophoresis to open channel structures with rectangular cross sections. Presented here is an examination of the results of continuous separations conducted under various experimental conditions. The characterization is conducted using analysis of both continuous and plug injections of material into the channel, and the parameters used to analyze the separation are lateral dispersion, longitudinal dispersion, and signal intensity. Longitudinal dispersion indicates the amount of band broadening in the direction parallel to channel flow and, therefore, determines the spatial resolution of the separation. Lateral dispersion corresponds to band broadening perpendicular to channel flow and affects the accuracy with which the time of sample introduction into the channel can be determined. The results from these experiments indicate that (a) a cooled channel system provides better results when longer analyses are conducted, (b) a capillary step rate yielding a band introduction angle of 45 degrees relative to the direction of flow in the channel provides the best compromise between longitudinal and lateral dispersions (this value typically equals 0.9 s/25-μm step for the system used in this research), (c) a capillary to channel linear velocity ratio of 3 to 5 yields improved signals relative to lower ratios due to more sample introduced (velocity ratios above this may lead to loss of spatial resolution), and (4) fast channel flows yield more symmetrically shaped bands than do slower flows due to more efficient transfer of material from the capillary-channel junction into the channel. Detection limits of 41 μM are obtained with a linear range from 0.12 mM to 1.9 mM for laser induced fluorescence detection.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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