Ultrasensitive PCR and real-time detection from human genomic samples using a bidirectional flow microreactor

被引:41
作者
Chen, Lin
West, Jonathan
Auroux, Pierre-Alain
Manz, Andreas
Day, Philip J. R.
机构
[1] Inst Analyt Sci, D-44139 Dortmund, Germany
[2] NIST, Elect Engn Lab, Gaithersburg, MD 20899 USA
[3] Univ Manchester, Manchester Interdisciplinary Bioctr, Manchester M1 7ND, Lancs, England
关键词
D O I
10.1021/ac701668k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this paper we present a reliable bidirectional flow DNA amplification microreactor for processing real-world genomic samples. This system shares the low-power thermal responsiveness of a continuous flow reactor with the low surface area to volume ratio character of stationary reactors for reducing surface inhibitory effects. Silanization with dimethyldichlorosilane in combination with dynamic surface passivation was used to enhance PCR compatibility and enable efficient amplification. For realtime fragment amplification monitoring we have implemented an epimodal fluorescent detection capability. The passivated bidirectional flow system was ultrasensitive, achieving an RNase P gene detection limit of 24 human genome copies with a reaction efficiency of 77%. This starts to rival the performance of a conventional real-time PCR instrument with a reaction efficiency of 93% and revitalizes flow-through PCR as a viable component of lab on a chip DNA analysis formats.
引用
收藏
页码:9185 / 9190
页数:6
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