Micellar electrokinetic chromatography for high-performance analytical separation
Autor: | Shigeru Terabe |
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Rok vydání: | 2008 |
Předmět: |
Analyte
Time Factors Chromatography Chemistry Capillary action General Chemical Engineering Analytical chemistry General Chemistry Separation principle Biochemistry Micelle Micellar electrokinetic chromatography Surface-Active Agents Electrophoresis chemistry.chemical_compound Capillary electrophoresis Materials Chemistry Sodium dodecyl sulfate Micelles Chromatography Micellar Electrokinetic Capillary |
Zdroj: | The Chemical Record. 8:291-301 |
ISSN: | 1528-0691 1527-8999 |
Popis: | Capillary electrophoresis (CE) is a relatively new method of analytical separation having the advantages of high separation efficiency, requirement of a small sample amount, low operating cost, and fast separation time. CE is a separation method where the analyte migrates under an electric field due to a charge on the analyte. Hence, CE was unable to separate neutral analytes until the advent of micellar electrokinetic chromatography (MEKC). MEKC is performed with an addition of ionic micelles to an electrophoretic medium, where a portion of the analyte is incorporated into the micelle and has an apparent charge, which can be subject to electrophoretic separation. The migration velocity of the neutral analyte in MEKC depends on what portion of the analyte is incorporated into the micelle. Thus, the separation principle of MEKC is similar to that of chromatography, although the micelle corresponding to the stationary phase in chromatography is not stationary inside the capillary. The fundamental characteristics and theoretical treatments of the behavior of the analyte in MEKC were studied extensively by the author's group. MEKC has been established as one of the most popular separation modes in CE. This review describes how MEKC was developed and how it is useful as a method of analytical separation. © 2008 The Japan Chemical Journal Forum and Wiley Periodicals, Inc. Chem Rec 8: 291–301; 2008: Published online in Wiley InterScience (www.interscience.wiley.com) DOI 10.1002/tcr.20156 |
Databáze: | OpenAIRE |
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