Hilton John P, Nguyen ThaiHuu, Barbu Mihaela, Pei Renjun, Stojanovic Milan, Lin Qiao
Department of Mechanical Engineering, Columbia University, New York, NY 10027, USA.
Division of Clinical Pharmacology and Experimental Therapeutics, Department of Medicine, Columbia University, New York, NY 10032, USA.
Microfluid Nanofluidics. 2012 Nov;13(5):749-760. doi: 10.1007/s10404-012-0993-8. Epub 2012 May 16.
We present a bead-based approach to microfluidic polymerase chain reaction (PCR), enabling fluorescent detection and sample conditioning in a single microchamber. Bead-based PCR, while not extensively investigated in microchip format, has been used in a variety of bioanalytical applications in recent years. We leverage the ability of bead-based PCR to accumulate fluorescent labels following DNA amplification to explore a novel DNA detection scheme on a microchip. The microchip uses an integrated microheater and temperature sensor for rapid control of thermal cycling temperatures, while the sample is held in a microchamber fabricated from (poly)dimethylsiloxane and coated with Parylene. The effects of key bead-based PCR parameters, including annealing temperature and concentration of microbeads in the reaction mixture, are studied to achieve optimized device sensitivity and detection time. The device is capable of detecting a synthetically prepared section of the genome in as few as 10 temperature cycles with times as short as 15 min. We then demonstrate the use of the procedure in an integrated device; capturing, amplifying, detecting, and purifying template DNA in a single microfluidic chamber. These results show that this method is an effective method of DNA detection which is easily integrated in a microfluidic device to perform additional steps such as sample pre-conditioning.
我们展示了一种基于微珠的微流控聚合酶链反应(PCR)方法,可在单个微腔室中实现荧光检测和样品预处理。基于微珠的PCR虽然在微芯片形式中未得到广泛研究,但近年来已用于各种生物分析应用中。我们利用基于微珠的PCR在DNA扩增后积累荧光标记的能力,探索一种在微芯片上的新型DNA检测方案。该微芯片使用集成的微型加热器和温度传感器来快速控制热循环温度,而样品则保存在由(聚)二甲基硅氧烷制成并涂有聚对二甲苯的微腔室中。研究了基于微珠的PCR关键参数的影响,包括退火温度和反应混合物中微珠的浓度,以实现优化的设备灵敏度和检测时间。该设备能够在短短15分钟内仅进行10个温度循环就能检测到合成制备的基因组片段。然后,我们展示了该程序在集成设备中的使用;在单个微流控腔室中捕获、扩增、检测和纯化模板DNA。这些结果表明,该方法是一种有效的DNA检测方法,易于集成到微流控设备中以执行诸如样品预处理等附加步骤。