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翻訳と辞書　辞書検索 [ 開発暫定版 ] スポンサード リンク micellar electrokinetic chromatography ： ウィキペディア英語版 micellar electrokinetic chromatography Micellar electrokinetic chromatography (MEKC), is a chromatography technique, used in analytical chemistry. It is a modification of capillary electrophoresis (CE), where the samples are separated by differential partitioning between micelles (pseudo-stationary phase) and a surrounding aqueous buffer solution (mobile phase).〔Terabe, S.; Otsuka, K.; Ichikawa, K.; Tsuchiya, A.; Ando, T. ''Anal. Chem''. 1984, ''56'', 111.〕 The basic set-up and detection methods used for MEKC are the same as those used in CE. The difference is that the solution contains a surfactant at a concentration that is greater than the critical micelle concentration (CMC). Above this concentration, surfactant monomers are in equilibrium with micelles. In most applications, MEKC is performed in open capillaries under alkaline conditions to generate a strong electroosmotic flow. Sodium dodecyl sulfate (SDS) is the most commonly used surfactant in MEKC applications. The anionic character of the sulfate groups of SDS cause the surfactant and micelles to have electrophoretic mobility that is counter to the direction of the strong electroosmotic flow. As a result, the surfactant monomers and micelles migrate quite slowly, though their net movement is still toward the cathode.〔Baker, D.R. “Capillary Electrophoresis” John Wiley & Sons, Inc.: New York, 1995.〕 During a MEKC separation, analytes distribute themselves between the hydrophobic interior of the micelle and hydrophilic buffer solution as shown in ''figure 1''. Analytes that are insoluble in the interior of micelles should migrate at the electroosmotic flow velocity, $u\_o$, and be detected at the retention time of the buffer, $t\_M$. Analytes that solubilize completely within the micelles (analytes that are highly hydrophobic) should migrate at the micelle velocity, $u\_c$, and elute at the final elution time, $t\_c$.〔Terabe, S.; Otsuka, K.; Ichikawa, K.; Tsuchiya, A.; Ando, T. ''Anal. Chem''. 1984, ''56'', 113.〕 == Theory == The micelle velocity is defined by: $u\_c=\; u\_p+u\_o$ where $u\_p$ is the electrophoretic velocity of a micelle.〔 The retention time of a given sample should depend on the capacity factor, $k^1$: $k^1=\backslash frac$ where $n\_c$ is the total number of moles of solute in the micelle and $n\_w$ is the total moles in the aqueous phase.〔 The retention time of a solute should then be within the range: $t\_M\backslash le\; t\_r\backslash le\; t\_c$ Charged analytes have a more complex interaction in the capillary because they exhibit electrophoretic mobility, engage in electrostatic interactions with the micelle, and participate in hydrophobic partitioning.〔Cunico,R.L.; Goodin, K.M.; Wehr,T. “Basic HPLC and CE of Biomolecules” Bay Bioanalytical Laboratory: Richmond, CA, 1998.〕 The fraction of the sample in the aqueous phase, $R$, is given by: $R=\; \backslash frac$ where $u\_s$ is the migration velocity of the solute.〔 The value $R$ can also be expressed in terms of the capacity factor: $R=\backslash frac$ Using the relationship between velocity, tube length from the injection end to the detector cell ($L$), and retention time, $u\_=\; L/t\_M$, $u\_=\; L/t\_$ and $u\_s\; =\; L/t\_r$, a relationship between the capacity factor and retention times can be formulated:〔 $k^1=\backslash frac$ The extra term enclosed in parenthesis accounts for the partial mobility of the hydrophobic phase in MEKC.〔 This equation resembles an expression derived for $k^1$ in conventional packed bed chromatography: $k=\backslash frac$ A rearrangement of the previous equation can be used to write an expression for the retention factor:〔Foley, J.P. ''Anal. Chem''. 1990, ''62'', 1302.〕 $t\_r\; =\backslash left\; (\; \backslash frac\; \backslash right\; )t\_M$ From this equation it can be seen that all analytes that partition strongly into the micellar phase (where $k^1$ is essentially ∞) migrate at the same time, $t\_c$. In conventional chromatography, separation of similar compounds can be improved by gradient elution. In MEKC, however, techniques must be used to extend the elution range to separate strongly retained analytes.〔 Elution ranges can be extended by several techniques including the use of organic modifiers, cyclodextrins, and mixed micelle systems. Short-chain alcohols or acetonitrile can be used as organic modifiers that decrease $t\_M$ and $k^1$ to improve the resolution of analytes that co-elute with the micellar phase. These agents, however, may alter the level of the EOF. Cyclodextrins are cyclic polysaccharides that form inclusion complexes that can cause competitive hydrophobic partitioning of the analyte. Since analyte-cyclodextrin complexes are neutral, they will migrate toward the cathode at a higher velocity than that of the negatively charged micelles. Mixed micelle systems, such as the one formed by combining SDS with the neutral surfactant Brij-35, can also be used to alter the selectivity of MEKC.〔 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「micellar electrokinetic chromatography」の詳細全文を読む スポンサード リンク 翻訳と辞書 : 翻訳のためのインターネットリソース Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.