An Yi-Quan, Huang Shao-Lei, Xi Bang-Chao, Gong Xiang-Lian, Ji Jun-Hao, Hu You, Ding Yi-Jie, Zhang Dong-Xu, Ge Sheng-Xiang, Zhang Jun, Xia Ning-Shao
State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, Department of Laboratory Medicine, School of Public Heath, Xiamen University, Xiamen 361102, China.
Micromachines (Basel). 2023 Mar 15;14(3):658. doi: 10.3390/mi14030658.
The polymerase chain reaction (PCR) is essential in nucleic acid amplification tests and is widely used in many applications such as infectious disease detection, tumor screening, and food safety testing; however, most PCR devices have inefficient heating and cooling ramp rates for the solution, which significantly limit their application in special scenarios such as hospital emergencies, airports, and customs. Here, we propose a temperature control strategy to significantly increase the ramp rates for the solution temperature by switching microfluidic chips between multiple temperature zones and excessively increasing the temperature difference between temperature zones and the solution; accordingly, we have designed an ultrafast thermocycler. The results showed that the ramp rates of the solution temperature are a linear function of temperature differences within a range, and a larger temperature difference would result in faster ramp rates. The maximum heating and cooling ramp rates of the 25 μL solution reached 24.12 °C/s and 25.28 °C/s, respectively, and the average ramp rate was 13.33 °C/s, 6-8 times higher than that of conventional commercial PCR devices. The thermocycler achieved 9 min (1 min pre-denaturation + 45 PCR cycles) ultrafast nucleic acid amplification, shortening the time by 92% compared to the conventional 120 min nucleic acid amplification, and has the potential to be used for rapid nucleic acid detection.
聚合酶链反应(PCR)在核酸扩增检测中至关重要,并且广泛应用于许多领域,如传染病检测、肿瘤筛查和食品安全检测;然而,大多数PCR设备对溶液的加热和冷却升温速率较低,这显著限制了它们在医院急诊、机场和海关等特殊场景中的应用。在此,我们提出一种温度控制策略,通过在多个温度区之间切换微流控芯片并过度增大温度区与溶液之间的温差,显著提高溶液温度的升温速率;据此,我们设计了一种超快速热循环仪。结果表明,在一定范围内,溶液温度的升温速率是温差的线性函数,温差越大,升温速率越快。25 μL溶液的最大加热和冷却升温速率分别达到24.12 °C/s和25.28 °C/s,平均升温速率为13.33 °C/s,比传统商用PCR设备高6 - 8倍。该热循环仪实现了9分钟(1分钟预变性 + 45个PCR循环)的超快速核酸扩增,与传统的120分钟核酸扩增相比,时间缩短了92%,具有用于快速核酸检测的潜力。