4.2 Article

Design and Implementation of Polymerase Chain Reaction Device for Aptamers Selection of Tumor Cells

期刊

JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
卷 20, 期 3, 页码 1332-1340

出版社

AMER SCIENTIFIC PUBLISHERS
DOI: 10.1166/jnn.2020.17356

关键词

PCR Amplification; Nucleic Acid Aptamer Selection; PID Algorithm; Temperature Control

资金

  1. NSFC [61527806]
  2. National Key Research and Development Program of China [2017YFA0205301]
  3. Hunan Key Research Project [2017SK2174]
  4. Natural Science Foundation of Hunan Province of China [2017JJ2069, 2018JJ3130]
  5. Economical Forest Cultivation and Utilization of 2011 Collaborative Innovation Center in Hunan Province [(2013) 448]

向作者/读者索取更多资源

Nucleic acid aptamers are a kind of one-dimensional biological nanomaterials and have found many applications. This paper designed and implemented a polymerase chain reaction (PCR) amplification device with a reaction volume of 500 mu L, which can be used for the amplification of nucleic acid aptamers of tumor cells in the aptamer selection. This device mainly includes a control module, a temperature measuring module, a PCR amplification tube, a metal tank module, a liquid crystal display (LCD) and operation module and a cooling module. The new PCR amplification chamber is matched with the designed metal tank to ensure the temperature uniformity of the PCR amplification solution. The control module based on the STM32F103RCT6 manages the workflow of the entire device. The PCR amplification chamber and PT100 sensors on the metal tank formed a closed-loop feedback system, and the incremental proportional-integral-derivative (PID) algorithm was used to achieve the precise temperature control. In addition, we introduced the Smith predictive compensation algorithm to solve the temperature hysteresis problem of the PCR amplification chamber. The experimental results showed that the PCR device can meet the requirements for the nucleic acid aptamer selection of tumor cells. The device can also be used in other experiments with large-volume PCR amplification.

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