Hofmann O, Che D, Cruickshank K A, Müller U R
Vysis, Inc., Downers Grove, Illinois 60515, USA.
Anal Chem. 1999 Feb 1;71(3):678-86. doi: 10.1021/ac9806660.
As a first step toward adaptation of capillary isoelectric focusing (cIEF) to microchannels on a glass chip, we have compared the three most common mobilization methods: chemical, hydrodynamic, and electroosmotic flow (EOF)-driven mobilization. Using a commercial cIEF apparatus with coated or uncoated fused-silica capillaries, both chemical and hydrodynamic mobilization gave superior separation efficiency and reproducibility. However, EOF-driven mobilization, which occurs simultaneously with focusing, proved most suitable for miniaturization because of high speed, EOF compatibility and low instrumentation requirements. When this method was tested in a 200-micron-wide, 10-micron-deep, and 7-cm-long channel etched into planar glass, a mixture of Cy5-labeled peptides could be focused in less than 30 s, with plate heights of 0.4 micron (410 plates/s) upon optimization. For a total analysis time of less than 5 min, we estimate a maximum peak capacity of approximately 30-40. Interestingly, the order of migration was found to be reversed compared to capillary-based focusing.
作为将毛细管等电聚焦(cIEF)应用于玻璃芯片微通道的第一步,我们比较了三种最常用的驱动方法:化学驱动、流体动力学驱动和电渗流(EOF)驱动。使用配有涂层或未涂层熔融石英毛细管的商用cIEF仪器,化学驱动和流体动力学驱动均具有更高的分离效率和重现性。然而,与聚焦同时发生的EOF驱动因速度快、与EOF兼容性好且仪器要求低,被证明最适合小型化。当在平面玻璃上蚀刻的200微米宽、10微米深、7厘米长的通道中测试此方法时,Cy5标记的肽混合物可在不到30秒内聚焦,优化后板高为0.4微米(410板/秒)。对于总分析时间少于5分钟的情况,我们估计最大峰容量约为30 - 40。有趣的是,发现迁移顺序与基于毛细管的聚焦相反。