首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >An extrusion fluidic driving method for continuous-flow polymerase chain reaction on a microfluidic chip
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An extrusion fluidic driving method for continuous-flow polymerase chain reaction on a microfluidic chip

机译:一种在微流控芯片上进行连续流聚合酶链反应的挤出流体驱动方法

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摘要

A novel extrusion driving protocol was developed based on micro-fabricated polydimethylsiloxane (PDMS) pneumatic valves. High efficiency liquid transfer was performed by using entirely overlapping control channels and fluid channels. A 0.5-s time is sufficient for the transfer of 9 μL sample solution between two chambers in the microchip with a nitrogen pressure of 70 kPa. The driving method was used in a microfluidic polymerase chain reaction (PCR) system, and rapid cycling of the PCR mixture in a closed loop was achieved. The amplification of DNA was demonstrated via both three-stage and two-stage PCR thermal cycling on the microchips resulting in significant reduction of the PCR time. The amplifications of 144-bp and 200-bp DNA fragments were achieved within 24 min using a three-stage protocol with 30 thermal cycles, and 130-bp DNA fragments within 12 min by using 20 thermal cycles in the two-stage system, compared to about 2 h in benchtop PCR with the same number of thermal cycles.
机译:基于微制造的聚二甲基硅氧烷(PDMS)气动阀,开发了一种新颖的挤出驱动方案。通过使用完全重叠的控制通道和流体通道进行高效液体传输。 0.5 s的时间足以在氮气压力为70 kPa的情况下在微芯片的两个腔室之间转移9μL样品溶液。该驱动方法用于微流体聚合酶链反应(PCR)系统中,并实现了PCR混合物在闭环中的快速循环。通过在微芯片上进行的三阶段和两阶段PCR热循环证明了DNA的扩增,从而大大缩短了PCR时间。相比之下,使用两阶段系统中的30个热循环的三阶段方案可在24分钟内完成144 bp和200 bp DNA片段的扩增,而在两阶段系统中使用20个热循环可在12分钟内实现130 bp DNA片段的扩增。在相同数量的热循环条件下,在台式PCR中约需2 h。

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