Thorslund Sara, Lindberg Peter, Andrén Per E, Nikolajeff Fredrik, Bergquist Jonas
Department of Engineering Sciences, Angström Laboratory, Uppsala University, Uppsala, Sweden.
Electrophoresis. 2005 Dec;26(24):4674-83. doi: 10.1002/elps.200500338.
A novel microsystem device in poly(dimethylsiloxane) (PDMS) for MS detection is presented. The microchip integrates sample injection, capillary electrophoretic separation, and electrospray emitter in a single substrate, and all modules are fabricated in the PDMS bulk material. The injection and separation flow is driven electrokinetically and the total amount of external equipment needed consists of a three-channel high-voltage power supply. The instant switching between sample injection and separation is performed through a series of low-cost relays, limiting the separation field strength to a maximum of 270 V/cm. We show that this set-up is sufficient to accomplish electrospray MS analysis and, to a moderate extent, microchip separation of standard peptides. A new method of instant in-channel oxidation makes it possible to overcome the problem of irreversibly bonded PDMS channels that have recovered their hydrophobic properties over time. The fast method turns the channel surfaces hydrophilic and less prone to nonspecific analyte adsorption, yielding better separation efficiencies and higher apparent peptide mobilities.
本文介绍了一种用于质谱检测的聚二甲基硅氧烷(PDMS)新型微系统装置。该微芯片在单个基底上集成了样品注入、毛细管电泳分离和电喷雾发射器,所有模块均在PDMS块状材料中制造。注入和分离流由电动驱动,所需的外部设备总量包括一个三通道高压电源。通过一系列低成本继电器实现样品注入和分离之间的即时切换,将分离场强限制在最大270 V/cm。我们表明,这种设置足以完成电喷雾质谱分析,并在一定程度上实现标准肽的微芯片分离。一种新的即时通道内氧化方法能够克服随着时间推移恢复了疏水特性的不可逆键合PDMS通道的问题。这种快速方法使通道表面具有亲水性,不易发生非特异性分析物吸附,从而产生更好的分离效率和更高的表观肽迁移率。