Battery-Powered Portable Rotary Real-Time Fluorescent qPCR with Low Energy Consumption, Low Cost, and High Throughput

被引:15
作者
He, Limin [1 ,2 ]
Sang, Benliang [1 ,2 ]
Wu, Wenming [1 ,2 ]
机构
[1] Chinese Acad Sci, State Key Lab Appl Opt, Changchun Inst Opt Fine Mech & Phys CIOMP, Changchun 130033, Jilin, Peoples R China
[2] Univ Chinese Acad Sci UCAS, Beijing 100049, Peoples R China
来源
BIOSENSORS-BASEL | 2020年 / 10卷 / 05期
基金
中国国家自然科学基金;
关键词
real-time PCR; portable; rotary; low cost; low energy consumption; high throughput; DNA AMPLIFICATION; VIRAL-RNA; PCR; VIRUS;
D O I
10.3390/bios10050049
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The traditional qPCR instrument is bulky, expensive, and inconvenient to carry, so we report a portable rotary real-time fluorescent PCR (polymerase chain reaction) that completes the PCR amplification of DNA in the field, and the reaction can be observed in real-time. Through the analysis of a target gene, namely pGEM-3Zf (+), the gradient amplification and melting curves are compared to commercial devices. The results confirm the stability of our device. This is the first use of a mechanical rotary structure to achieve gradient amplification curves and melting curves comparable to commercial instruments. The average power consumption of our system is about 7.6 W, which is the lowest energy consumption for real-time fluorescence quantification in shunting PCR and enables the use of our device in the field thanks to its self-contained power supply based on a lithium battery. In addition, all of the equipment costs only about 710 dollars, which is far lower than the cost of a commercial PCR instrument because the control system through mechanical displacement replaces the traditional TEC (thermoelectric cooler) temperature control. Moreover, the equipment has a low technical barrier, which can suit the needs of non-professional settings, with strong repeatability.
引用
收藏
页数:11
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共 27 条
  • [1] Handheld real-time PCR device
    Ahrberg, Christian D.
    Ilic, Bojan Robert
    Manz, Andreas
    Neuzil, Pavel
    [J]. LAB ON A CHIP, 2016, 16 (03) : 586 - 592
  • [2] Basic principles of real-time quantitative PCR
    Arya, M
    Shergill, IS
    Williamson, M
    Gommersall, L
    Arya, N
    Patel, HRH
    [J]. EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2005, 5 (02) : 209 - 219
  • [3] Bialek H., 2016, P 2016 IEEE EMBS INT, P1
  • [4] Real-time reverse transcription PCR (qRT-PCR) and its potential use in clinical diagnosis
    Bustin, SA
    Mueller, R
    [J]. CLINICAL SCIENCE, 2005, 109 (04) : 365 - 379
  • [5] Identification of A/H5N1 influenza viruses using a single gene diagnostic microarray
    Dawson, Erica D.
    Moore, Chad L.
    Dankbar, Daniela M.
    Mehlmann, Martin
    Townsend, Michael B.
    Smagala, James A.
    Smith, Catherine B.
    Cox, Nancy J.
    Kuchta, Robert D.
    Rowlen, Kathy L.
    [J]. ANALYTICAL CHEMISTRY, 2007, 79 (01) : 378 - 384
  • [6] Ellis J, 2009, EUROSURVEILLANCE, V14
  • [7] Real time quantitative PCR
    Heid, CA
    Stevens, J
    Livak, KJ
    Williams, PM
    [J]. GENOME RESEARCH, 1996, 6 (10): : 986 - 994
  • [8] Rapid quantification of hepatitis B virus DNA by real-time PCR using fluorescent hybridization probes
    Ho, SKN
    Yam, WC
    Leung, ETK
    Wong, LP
    Leung, JKH
    Lai, KN
    Chan, TM
    [J]. JOURNAL OF MEDICAL MICROBIOLOGY, 2003, 52 (05) : 397 - 402
  • [9] Application of automatic feedback photographing by portable smartphone in PCR
    Jiang, Yangyang
    Li, Bin
    Wu, Wenming
    [J]. SENSORS AND ACTUATORS B-CHEMICAL, 2019, 298
  • [10] Ultrafast Rotary PCR system for multiple influenza viral RNA detection
    Jung, Jae Hwan
    Choi, Seok Jin
    Park, Byung Hyun
    Choi, Young Ki
    Seo, Tae Seok
    [J]. LAB ON A CHIP, 2012, 12 (09) : 1598 - 1600