University of Virginia, USA.
MicroGEM International, PLC, USA.
Lab Chip. 2022 Sep 13;22(18):3424-3435. doi: 10.1039/d2lc00495j.
The polymerase chain reaction (PCR) is paramount in nucleic acid amplification testing, and for many assays, the use of PCR or qPCR is considered the 'gold standard'. While instrumentation for executing PCR has advanced over the last two decades, a growing interest in point-of-need testing has highlighted the deficit that exists for 'rapid PCR' systems. Here, we describe a field-forward prototype instrument capable of ultra-fast thermal cycling for real-time PCR amplification of DNA and RNA. The custom-designed, injection-molded microfluidic chips interface with a novel mechatronic system to complete 40 cycles of real-time PCR in under 10 minutes, an 84% reduction in time compared to a standard 50 minute assay. Such rapid amplification is enabled by two thermoelectric Peltiers capable of efficiently heating and cooling the sample at 12 and 10 °C s, respectively. Judicious selection and strategic placement of the thermal cyclers and fluorescence detector relative to the microchip enable synchronized thermal cycling and fluorescence monitoring, further reducing time-to-result. Robust amplification and detection of DNA and RNA targets empowers laboratories to achieve rapid, actionable information in endless applications.
聚合酶链反应(PCR)是核酸扩增测试中的关键技术,对于许多检测方法,PCR 或 qPCR 的使用被认为是“金标准”。虽然过去二十年来执行 PCR 的仪器已经得到了改进,但对即时检测的兴趣日益浓厚,突显了“快速 PCR”系统存在的不足。在这里,我们描述了一种具有前瞻性的现场原型仪器,能够实现用于 DNA 和 RNA 实时 PCR 扩增的超快速热循环。定制设计的注塑微流控芯片与新颖的机电系统接口,可在不到 10 分钟内完成 40 个循环的实时 PCR,与标准的 50 分钟检测相比,时间减少了 84%。这种快速扩增是通过两个热电冷却器实现的,它们能够分别以 12 和 10°C/s 的速度高效地加热和冷却样品。热循环器和荧光探测器相对于微芯片的明智选择和战略放置实现了同步热循环和荧光监测,进一步缩短了结果时间。对 DNA 和 RNA 靶标的稳健扩增和检测使实验室能够在各种应用中实现快速、可行的信息。