Chen Zongyuan, Qian Shizhi, Abrams William R, Malamud Daniel, Bau Haim H
Department of Mechanical Engineering and Applied Mechanics, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA 19104-6315, USA.
Anal Chem. 2004 Jul 1;76(13):3707-15. doi: 10.1021/ac049914k.
A self-actuated, flow-cycling polymerase chain reaction (PCR) reactor that takes advantage of buoyancy forces to continuously circulate reagents in a closed loop through various thermal zones has been constructed, tested, and modeled. The heating required for the PCR is advantageously used to induce fluid motion without the need for a pump. Flow velocities on the order of millimeters per second are readily attainable. In our preliminary prototype, we measured a cross-sectionally averaged velocity of 2.5 mm/s and a cycle time of 104 s. The flow velocity is nearly independent of the loop's length, making the device readily scalable. Successful amplifications of 700- and 305-bp fragments of Bacillus cereus genomic DNA have been demonstrated. Since the device does not require any moving parts, it is particularly suitable for miniature systems.
一种利用浮力使试剂在封闭回路中连续循环通过不同热区的自驱动、流量循环聚合酶链反应(PCR)反应器已被构建、测试和建模。PCR所需的加热被有利地用于诱导流体运动,而无需泵。每秒毫米量级的流速很容易实现。在我们的初步原型中,我们测量到横截面平均流速为2.5毫米/秒,循环时间为104秒。流速几乎与回路长度无关,这使得该装置易于扩展。已证明成功扩增了蜡样芽孢杆菌基因组DNA的700和305碱基对片段。由于该装置不需要任何活动部件,因此特别适用于微型系统。