Xu Zhongqi, Nakamura Yousuke, Hirokawa Takeshi
Applied Chemistry, Department of Chemistry and Chemical Engineering, Graduate School of Engineering, Hiroshima University, Kagamiyama, Higashi-hiroshima, Japan.
Electrophoresis. 2005 Jan;26(2):383-90. doi: 10.1002/elps.200410151.
Fundamental understanding of the impact of reservoir potentials on the analyte behavior on the microfluidic chips is an important issue in microchip electrophoresis (MCE) for suitable injection and separation of analytes, since the applied potentials may significantly affect the shape of sample plug, sample leakage from the injection channel to the separation channel, injected sample amount, and separation efficiency. This study addressed this issue for the case of a conventional cross-geometry microchip with four reservoirs using computer simulations, the results of which were verified by the analysis of DNA fragments. For the microchip with a definite structure and migration distance, the injected sample amount was shown to be the vital parameter for improving the limit of detection and resolution. During injection, the shape of the sample plug could be adjusted by varying the reservoir potentials. It was demonstrated that a "magnified injection" (applying high voltage on the three reservoirs to the sample reservoir) is useful to enhance the detection sensitivity depending on the analyte composition, although such injection was previously avoided because of introducing too large amounts of the analyte in comparison with two established modes, floating and pinched injection. Optimal magnified injection was proved to improve the sensitivity for about 4 times over that of pinched injection for the analysis of DNA step ladders using microchip gel electrophoresis (MCGE). Sample leakage of DNA fragments could be suppressed by applying a high positive voltage on injection channel during separation, but the voltage degraded the injected amount and resolution.
深入理解储液器电位对微流控芯片上分析物行为的影响,对于微芯片电泳(MCE)中实现分析物的合适进样和分离而言是一个重要问题,因为所施加的电位可能会显著影响样品塞的形状、样品从进样通道泄漏到分离通道的情况、进样量以及分离效率。本研究针对具有四个储液器的传统交叉结构微芯片的情况,通过计算机模拟解决了这一问题,其结果通过对DNA片段的分析得到了验证。对于具有确定结构和迁移距离的微芯片,进样量被证明是提高检测限和分辨率的关键参数。在进样过程中,可以通过改变储液器电位来调整样品塞的形状。结果表明,“放大进样”(在三个储液器上对样品储液器施加高电压)有助于根据分析物组成提高检测灵敏度,尽管由于与两种既定模式(浮动进样和夹断进样)相比会引入过多的分析物,这种进样方式此前一直被避免使用。对于使用微芯片凝胶电泳(MCGE)分析DNA阶梯,经证明最佳放大进样比夹断进样的灵敏度提高约4倍。在分离过程中,通过在进样通道上施加高正电压,可以抑制DNA片段的样品泄漏,但该电压会降低进样量和分辨率。