Dept. of Computer Engineering, Hallym University, Chuncheon, South Korea.
Bio-IT Research Center, Hallym University, Chuncheon, South Korea.
Biomed Eng Online. 2018 Nov 6;17(Suppl 2):156. doi: 10.1186/s12938-018-0579-0.
Polymerase chain reaction (PCR) is used in nucleic acid tests of infectious diseases in point-of-care testing. Previous studies have demonstrated real-time PCR that uses a micro-PCR chip made of packing tape, double-sided tape, and a plastic cover with polycarbonate or polypropylene on a black matte printed circuit board substrate. Despite the success of DNA amplification and fluorescence detection using an early version of the micro-PCR chip, reaching the target temperature was fairly slow and, as a result, the total running time was getting longer. To reduce this runtime, the micro-PCR chip was modified by reducing the heater pattern size of the PCB substrate to one-quarter of the original size or less, while maintaining the ability of the heating pattern to cover the reservoir area of the microfluidic channel. In subsequent experiments, DNA amplification failed several times. During the analysis of the cause of this failure, it was found that the reagent was boiling with the heating range from 25 to 95 °C.
As a method of DNA amplification verification, images were captured by digital single-lens reflex camera to detect FAM fluorescence using diagonal illumination from a blue LED light source. The images were automatically captured at 72 °C (the extension step in nucleic acid amplification) and the brightness of the captured images was analyzed to con-firm the success of DNA amplification.
Compared to the previous chip with a larger heating pattern size, the current chip appears to generate excess energy as the size of the heating pattern was reduced. To reduce this excess energy, the initial voltage was lowered to 2 V and 2.5 V, which is equivalent to a one-fifth and one-quarter voltage-power reduction in pulse width modulation control, respectively. In both voltage reduction cases, the DNA amplification was successful.
DNA amplification tests may fail due to the excess energy generated by reducing the heater pattern size of the PCB substrate. However, the tests succeeded when the voltage was reduced to 2 V or 2.5 V. The 2.5 V power test was more efficient for reducing the overall running time.
聚合酶链式反应(PCR)用于即时护理检测中的传染病核酸检测。先前的研究已经证明了使用包装胶带、双面胶带和带有聚碳酸酯或聚丙烯的塑料盖制成的微 PCR 芯片的实时 PCR,该芯片位于黑色亚光印刷电路板衬底上。尽管使用早期版本的微 PCR 芯片成功地进行了 DNA 扩增和荧光检测,但达到目标温度的速度相当慢,因此总运行时间越来越长。为了缩短运行时间,将微 PCR 芯片的 PCB 衬底的加热图案尺寸缩小到原始尺寸的四分之一或更小,同时保持加热图案覆盖微流道储液器区域的能力。在随后的实验中,DNA 扩增多次失败。在分析失败原因的过程中,发现试剂在 25 至 95°C 的加热范围内沸腾。
作为 DNA 扩增验证的一种方法,使用数字单镜头反光相机拍摄图像,使用蓝色 LED 光源的对角线照明检测 FAM 荧光。图像在 72°C(核酸扩增的延伸步骤)自动捕获,并分析捕获图像的亮度以确认 DNA 扩增的成功。
与之前加热图案尺寸较大的芯片相比,当前芯片在减小加热图案尺寸时似乎会产生过多的能量。为了减少这种多余的能量,将初始电压降低到 2V 和 2.5V,这分别相当于脉宽调制控制的五分之一和四分之一电压功率降低。在这两种电压降低的情况下,DNA 扩增都成功了。
DNA 扩增测试可能会因减小 PCB 衬底加热图案尺寸而导致能量过剩而失败。但是,当电压降低到 2V 或 2.5V 时,测试就成功了。2.5V 功率测试在降低整体运行时间方面更有效。