三种不同微乳液体系作为毛细管电泳分离酮类测试溶质的缓冲液的比较

H. Watarai, I. Takahashi
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引用次数: 12

摘要

以阴离子、非离子和阳离子油水溶液(0 /w)为分离介质,以萘为荧光基团间接荧光检测,研究了酮类和β-二酮类的毛细管电泳行为。迁移行为在很大程度上取决于微乳液的电荷类型、组成和ph值。在所研究的体系中,十二烷基硫酸钠(SDS)微乳液因其更宽的分离窗口、更高的溶解能力和更快的分布速率而最具优势。SDS微乳电泳中溶质的容量因子与其在两相体系中的分布和界面吸附参数相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of three different microemulsion systems as the run buffer for the capillary electrophoretic separation of ketone test solutes
Capillary electrophoretic behavior of ketones and β-diketones was examined using anionic, nonionic and cationic oil in water (o/w) microemulsions as separation media, containing naphthalene as a fluorophore for means of indirect fluorescence detection. The migration behavior was greatly dependent on the charge type of microemulsions as well as on the composition and pH. Among the systems examined, sodium dodecyl sulfate (SDS) microemulsions were the most advantageous because of the wider separation window, the higher dissolution capacity and the rapid distribution rate. Capacity factors of the solutes in the electrophoresis employing SDS microemulsions were correlated to the distribution and interfacial adsorption parameters determined in bulk two-phase systems.
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