Liljegren Gustav, Dahlin Andreas, Zettersten Camilla, Bergquist Jonas, Nyholm Leif
Department of Analytical Chemistry, Uppsala University, Box 599, SE-751 24 Uppsala, Sweden.
Lab Chip. 2005 Oct;5(10):1008-16. doi: 10.1039/b506289f. Epub 2005 Aug 10.
A novel method for the manufacturing of microchips for on-chip combinations of electrochemistry (EC) and sheathless electrospray ionisation mass spectrometry (ESI-MS) is described. The technique, which does not require access to clean-room facilities, is based on the incorporation of an array of gold microcoil electrodes into a poly(dimethylsiloxane)(PDMS) microflow channel equipped with an integrated graphite based sheathless ESI emitter. Electrochemical measurements, which were employed to determine the electroactive area of the electrodes and to test the microchips, show that the manufacturing process was reproducible and that the important interelectrode distance in the electrochemical cell could to be adequately controlled. The EC-ESI-MS device was evaluated based on the ESI-MS detection of the oxidation products of dopamine. The results demonstrate that the present on-chip approach enables full potentiostatic control of the electrochemical cell and the attainment of very short transfer times between the electrochemical cell and the electrospray emitter. The transfer times were 0.6 and 1.2 s for flow rates of 1.0 and 0.5 microL min(-1), respectively, while the electrochemical conversion efficiency of the electrochemical cell was found to be 30% at a flow rate of 0.5 microL min(-1). To decouple the electrochemical cell from the ESI-MS high voltage and to increase the user-friendliness, the on-line electrochemistry-ESI-MS experiments were performed using a wireless Bluetooth battery-powered instrument with the chip floating at the potential induced by the ESI high voltage. The described on-chip EC-ESI-MS device can be used for fundamental electrochemical investigations as well as for applications based on the use of electrochemically controlled sample pretreatment, preconcentration and ionisation steps prior to ESI-MS.
本文描述了一种制造用于电化学(EC)与无鞘电喷雾电离质谱(ESI-MS)片上联用的微芯片的新方法。该技术不需要使用洁净室设施,其原理是将一系列金微线圈电极集成到一个配备了基于石墨的集成无鞘ESI发射器的聚二甲基硅氧烷(PDMS)微流通道中。用于确定电极电活性面积和测试微芯片的电化学测量结果表明,制造过程具有可重复性,并且电化学池中重要的电极间距能够得到充分控制。基于多巴胺氧化产物的ESI-MS检测对EC-ESI-MS装置进行了评估。结果表明,目前的片上方法能够实现对电化学池的完全恒电位控制,并能在电化学池和电喷雾发射器之间实现非常短的转移时间。流速为1.0和0.5 μL min⁻¹时,转移时间分别为0.6和1.2 s,而在流速为0.5 μL min⁻¹时,电化学池的电化学转换效率为30%。为了使电化学池与ESI-MS高压解耦并提高用户友好性,在线电化学-ESI-MS实验使用了一种无线蓝牙电池供电仪器,芯片在ESI高压感应的电位下浮动。所描述的片上EC-ESI-MS装置可用于基础电化学研究,以及基于在ESI-MS之前使用电化学控制的样品预处理、预浓缩和电离步骤的应用。