Kim Jitae, Byun Doyoung, Mauk Michael G, Bau Haim H
Department of Mechanical Engineering and Applied Mechanics, University of Pennsylvania, Philadelphia, PA 19104-6315, USA.
Lab Chip. 2009 Feb 21;9(4):606-12. doi: 10.1039/b807915c. Epub 2008 Nov 18.
A disposable, self-contained polymerase chain reaction (PCR) chip with on-board stored, just-on-time releasable, paraffin-passivated, dry reagents is described. During both storage and sample preparation, the paraffin immobilizes and protects the stored reagents. Fluid flow through the reactor leaves the reagents undisturbed. Prior to the amplification step, the chamber is filled with target analyte suspended in water. Upon heating the PCR chamber to the DNA's denaturation temperature, the paraffin melts and moves out of the way, and the reagents are released and hydrated. To better understand the reagent release process, a scaled up model of the reactor was constructed and the paraffin migration was visualized. Experiments were carried out with a 30 microl reactor demonstrating detectable amplification (with agarose gel electrophoresis) of 10 fg ( approximately 200 copies) of lambda DNA template. The in-reactor storage and on-time release of the PCR reagents reduce the number of needed operations and significantly simplifies the flow control that would, otherwise, be needed in lab-on-chip devices.
描述了一种一次性、独立的聚合酶链反应(PCR)芯片,其带有在芯片上储存、可即时释放、经石蜡钝化的干燥试剂。在储存和样品制备过程中,石蜡固定并保护储存的试剂。流体流经反应器时不会扰动试剂。在扩增步骤之前,向反应腔中加入悬浮于水中的目标分析物。将PCR反应腔加热至DNA变性温度时,石蜡熔化并移开,试剂被释放并水化。为了更好地理解试剂释放过程,构建了反应器的放大模型并可视化石蜡迁移。使用30微升反应器进行的实验表明,对10飞克(约200个拷贝)的λDNA模板进行了可检测到的扩增(通过琼脂糖凝胶电泳)。PCR试剂在反应器内的储存和即时释放减少了所需的操作数量,并显著简化了芯片实验室设备中原本所需的流动控制。