Hsieh Yi-Fan, Lee Da-Sheng, Chen Ping-Hei, Liao Shao-Kai, Yeh Shiou-Hwei, Chen Pei-Jer, Yang An-Shik
Department of Mechanical Engineering, National Taiwan University, Taipei 106, Taiwan.
Department of Energy and Refrigerating Air-Conditioning Engineering, National Taipei University of Technology, Taipei 106, Taiwan.
Sens Actuators B Chem. 2013 Jul 5;183:434-440. doi: 10.1016/j.snb.2013.04.003. Epub 2013 Apr 11.
This research reports the design, analysis, integration, and test of a prototype of a real-time convective polymerase chain reaction (RT-cPCR) machine that uses a color charged coupled device (CCD) for detecting the emission of fluorescence intensity from an RT-cPCR mix in a microliter volume glass capillary. Because of its simple mechanism, DNA amplification involves employing the cPCR technique with no need for thermocycling control. The flow pattern and temperature distribution can greatly affect the cPCR process in the capillary tube, a computational fluid dynamics (CFD) simulation was conducted in this study for the first time to estimate the required period of an RT-cPCR cycle. This study also tested the PCR mix containing hepatitis B virus (HBV) plasmid samples by using SYBR Green I fluorescence labeling dye to assess the prototype performance. The measured results from the image-processing scheme indicate that the RT-cPCR prototype with a CCD-based fluorometer can achieve similar DNA quantification reproducibility compared to commercial machines, even when the initial DNA concentration in the test PCR mix is reduced to 10 copies/μL.
本研究报告了一种实时对流聚合酶链反应(RT-cPCR)机器原型的设计、分析、集成和测试。该机器使用彩色电荷耦合器件(CCD)来检测微升体积玻璃毛细管中RT-cPCR混合物的荧光强度发射。由于其机制简单,DNA扩增采用cPCR技术,无需热循环控制。流动模式和温度分布会极大地影响毛细管中的cPCR过程,本研究首次进行了计算流体动力学(CFD)模拟,以估计RT-cPCR循环所需的时间。本研究还通过使用SYBR Green I荧光标记染料测试了含有乙型肝炎病毒(HBV)质粒样本的PCR混合物,以评估该原型的性能。图像处理方案的测量结果表明,即使测试PCR混合物中的初始DNA浓度降至10拷贝/μL,基于CCD的荧光计的RT-cPCR原型与商用机器相比仍可实现相似的DNA定量重现性。