MICROFLUIDIC FLOW-THROUGH REACTOR WITH ELECTROCHEMICAL SENSOR ARRAY FOR REAL-TIME PCR

被引:1
|
作者
Huey-Fang, Teh [1 ]
Ramalingam, Naveen [1 ]
Hai-Qing, Gong [1 ]
Swee-Ngin, Tan [2 ]
机构
[1] Nanyang Technol Univ, Sch Mech & Aerosp Engn, BioMEMS Lab, Singapore 639798, Singapore
[2] Nanyang Technol Univ, Natl Inst Educ, Div Nat Sci, Singapore 639798, Singapore
来源
MODERN PHYSICS LETTERS B | 2009年 / 23卷 / 03期
关键词
Flow-through PCR microdevice; real-time quantification PCR; electrochemical detection; AMPLIFICATION;
D O I
10.1142/S0217984909018424
中图分类号
O59 [应用物理学];
学科分类号
摘要
We developed an integrated microfluidic flow-through EC-PCR (EC-PCR) microdevice for the concurrent DNA amplification, PCR products EC detection and PCR products quantification instead of the current available fluorescence detection scheme. The microfluidic flow-through EC-PCR microdevice was fabricated with the state-of-the-art microfabrication technology, by bonding a bottom glass substrate having a microelectrode array to a top glass cover having the microchannels made of PDMS material. Both the amplification of the target DNA sequence and the subsequent EC detection of the PCR products were carried out concurrently on the integrated device by real-time monitoring. The underlying principle of the microfluidic flow-through EC-PCR method was based on the changes of current signal of methylene blue (MB), which worked as an electrochemically active species DNA intercalator in the PCR mixture, during the amplification process at the extension phase. The results shown in this work indicated that the nucleic acid analysis could be performed in a fast thermal cycling and true real-time quantitative electrochemical detection. The signal variation trends of the EC detection and the fluorescence detection were the same in our verification measurements for both methods, which suggested that the EC detection method was feasible for this application.
引用
收藏
页码:369 / 372
页数:4
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