Xiangfu Laboratory, Jiashan 314100, China.
State Key Laboratory of Transducer Technology, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050, China.
Biosensors (Basel). 2024 Aug 6;14(8):379. doi: 10.3390/bios14080379.
In the rapid development of molecular biology, nucleic acid amplification detection technology has received more and more attention. The traditional polymerase chain reaction (PCR) instrument has poor refrigeration performance during its transition from a high temperature to a low temperature in the temperature cycle, resulting in a longer PCR amplification cycle. Peltier element equipped with both heating and cooling functions was used, while the robust adaptive fuzzy proportional integral derivative (PID) algorithm was also utilized as the fundamental temperature control mechanism. The heating and cooling functions were switched through the state machine mode, and the PCR temperature control module was designed to achieve rapid temperature change. Cycle temperature test results showed that the fuzzy PID control algorithm was used to accurately control the temperature and achieve rapid temperature rise and fall (average rising speed = 11 °C/s, average falling speed = 8 °C/s) while preventing temperature overcharging, maintaining temperature stability, and achieving ultra-fast PCR amplification processes (45 temperature cycle time < 19 min). The quantitative results show that different amounts of fluorescence signals can be observed according to the different concentrations of added viral particles, and an analytical detection limit (LoD) as low as 10 copies per μL can be achieved with no false positive in the negative control. The results show that the TEC amplification of nucleic acid has a high detection rate, sensitivity, and stability. This study intended to solve the problem where the existing thermal cycle temperature control technology finds it difficult to meet various new development requirements, such as the rapid, efficient, and miniaturization of PCR.
在分子生物学的快速发展中,核酸扩增检测技术受到了越来越多的关注。传统的聚合酶链反应(PCR)仪器在温度循环中从高温到低温的转换过程中制冷性能较差,导致 PCR 扩增周期较长。采用了同时具备加热和冷却功能的 Peltier 元件,并利用强大的自适应模糊比例积分微分(PID)算法作为基本的温度控制机制。通过状态机模式切换加热和冷却功能,设计了 PCR 温度控制模块以实现快速温度变化。循环温度测试结果表明,模糊 PID 控制算法可精确控制温度,实现快速升温降温和防止温度过冲,保持温度稳定性,并实现超快速的 PCR 扩增过程(45 个温度循环时间<19 分钟)。定量结果表明,根据添加的病毒颗粒的不同浓度,可以观察到不同量的荧光信号,并且在阴性对照中没有假阳性,可达到低至 10 拷贝/μL 的分析检测限(LoD)。结果表明,TEC 核酸扩增具有高检测率、灵敏度和稳定性。本研究旨在解决现有热循环温度控制技术难以满足各种新发展要求的问题,如 PCR 的快速、高效和小型化。