Liu Dayu, Ou Ziyou, Xu Mingfei, Wang Lihui
Bioengineering Center, Improve Medical Instrument's Co., Ltd., 510370 Guangzhou, China.
J Chromatogr A. 2008 Dec 19;1214(1-2):165-70. doi: 10.1016/j.chroma.2008.10.066. Epub 2008 Oct 21.
We present a sensitive, simple and robust on-chip transient isotachophoresis/capillary gel electrophoresis (tITP/CGE) method for the analysis of polymerase chain reaction (PCR) samples. Using chloride ions in the PCR buffer and N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid (HEPES) in the background electrolyte, respectively, as the leading and terminating electrolytes, the tITP preconcentration was coupled with CGE separation with double-T shaped channel network. The tITP/CGE separation was carried out with a single running buffer. The separation process involved only two steps that were performed continuously with the sequential switching of four voltage outputs. The tITP/CGE method showed an analysis time and a separation efficiency comparable to those of standard CGE, while the signal intensity was enhanced by factors of over 20. The limit of detection of the chip-based tITP/CGE method was estimated to be 1.1 ng/mL of DNA in 1x PCR buffer using confocal fluorescence detection following 473 nm laser excitation.
我们展示了一种灵敏、简单且稳健的芯片上瞬态等速电泳/毛细管凝胶电泳(tITP/CGE)方法,用于分析聚合酶链反应(PCR)样品。分别使用PCR缓冲液中的氯离子和背景电解质中的N-2-羟乙基哌嗪-N'-2-乙磺酸(HEPES)作为前导电解质和终止电解质,tITP预浓缩与具有双T形通道网络的CGE分离相结合。tITP/CGE分离使用单一运行缓冲液进行。分离过程仅涉及两个步骤,通过依次切换四个电压输出连续进行。tITP/CGE方法的分析时间和分离效率与标准CGE相当,而信号强度提高了20倍以上。在473nm激光激发后,使用共聚焦荧光检测,基于芯片的tITP/CGE方法的检测限估计为1x PCR缓冲液中1.1ng/mL的DNA。