MCU based real-time temperature control system for universal microfluidic PCR chip

被引:12
|
作者
Han, Dawoon [1 ]
Jang, You-Cheol [2 ]
Oh, Sung-Nam [3 ]
Chand, Rohit [1 ]
Lim, Ki-Tae [1 ]
Kim, Kab-Il [3 ]
Kim, Yong-Sang [1 ]
机构
[1] Sungkyunkwan Univ, Sch Elect & Elect Engn, Suwon 440746, Gyeonggi, South Korea
[2] STATSChipPac, Dept Res & Dev, Inchon 467734, Gyeonggi, South Korea
[3] Myongji Univ, Dept Elect Engn, Yongin 449728, Gyeonggi, South Korea
来源
MICROSYSTEM TECHNOLOGIES-MICRO-AND NANOSYSTEMS-INFORMATION STORAGE AND PROCESSING SYSTEMS | 2014年 / 20卷 / 03期
关键词
DIAGNOSTICS; FABRICATION; GLASS;
D O I
10.1007/s00542-013-1970-1
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
The analysis of genetic materials in the post-human genome project era has become an ever-expanding branch of research and thus routinely employed in majority of biochemical laboratories. Most of the diagnostic research area emphasizes on polymerase chain reaction for detecting pathogenic organisms. However, the conventional polymerase chain reaction requires expensive and sophisticated thermal cycler and is not handy owing to its large dimensions. Therefore, we fabricated a continuous-flow polymerase chain reaction chip on a PDMS based microfluidic platform to ease the hardship of the conventional system. Temperature being the most crucial factor in polymerase chain reaction, was monitored and regulated by thermostatic action using an on-line computer system. Indium tin oxide coated glass platform was used for heating as it is transparent and has good thermal conductivity under the influence of DC bias. The heating circuit used an ATMega 128 MCU to control the temperature. As a result, a precise and quick heating environment was maintained on the microfluidic chip to amplify the target DNA. We successfully amplified Lambda phage and Escherichia coli DNA on our chip to prove the practicality of the device.
引用
收藏
页码:471 / 476
页数:6
相关论文
共 50 条
  • [21] Laboratory Diagnosis of 37 Cases of Bartonella Endocarditis Based on Enzyme Immunoassay and Real-Time PCR
    Shapira, Lev
    Rasis, Michal
    Ehrenreich, Inbal Binsky
    Maor, Yasmin
    Katchman, Eugene A.
    Treves, Adi
    Velan, Ariel
    Halutz, Ora
    Graidy-Varon, Merav
    Leibovitch, Cecilia
    Maisler, Noam
    Ephros, Moshe
    Giladi, Michael
    JOURNAL OF CLINICAL MICROBIOLOGY, 2021, 59 (06)
  • [22] Real-time measurement of flow rate in microfluidic devices using a cantilever-based optofluidic sensor
    Cheri, Mohammad Sadegh
    Latifi, Hamid
    Sadeghi, Jalal
    Moghaddam, Mohammadreza Salehi
    Shahraki, Hamidreza
    Hajghassem, Hasan
    ANALYST, 2014, 139 (02) : 431 - 438
  • [23] Comparison of multiplexed-tandem real-time PCR panel with reference real-time PCR molecular diagnostic assays for detection of Giardia intestinalis and Tritrichomonas foetus in cats
    Meggiolaro, Maira N.
    Roeber, Florian
    Kobylski, Victoria
    Higgins, Damien P.
    Slapeta, Jan
    VETERINARY PARASITOLOGY, 2019, 266 : 12 - 17
  • [24] Performance of a real-time PCR-based approach and droplet digital PCR in detecting human parechovirus type 3 RNA
    Aizawa, Yuta
    Koyama, Akihide
    Ishihara, Tomohiko
    Onodera, Osamu
    Saitoh, Akihiko
    JOURNAL OF CLINICAL VIROLOGY, 2016, 84 : 27 - 31
  • [25] Characterization and analysis of real-time capillary convective PCR toward commercialization
    Qiu, Xianbo
    Zhang, Shiyin
    Mei, Lanju
    Wu, Di
    Guo, Qi
    Li, Ke
    Ge, Shengxiang
    Ye, Xiangzhong
    Xia, Ningshao
    Mauk, Michael G.
    BIOMICROFLUIDICS, 2017, 11 (02):
  • [26] Partial validation of a TaqMan real-time quantitative PCR for the detection of ranaviruses
    Stilwell, Natalie K.
    Whittington, Richard J.
    Hick, Paul M.
    Becker, Joy A.
    Ariel, Ellen
    van Beurden, Steven
    Vendramin, Niccolo
    Olesen, Niels J.
    Waltzek, Thomas B.
    DISEASES OF AQUATIC ORGANISMS, 2018, 128 (02) : 105 - 116
  • [27] Conventional PCR and Real-time Quantitative PCR Detection of Helminthosporium Solani in Soil and on Potato Tubers
    Danny W. Cullen
    Alison K. Lees
    Ian K. Toth
    James M. Duncan
    European Journal of Plant Pathology, 2001, 107 : 387 - 398
  • [28] Conventional PCR and real-time quantitative PCR detection of Helminthosporium solani in soil and on potato tubers
    Cullen, DW
    Lees, AK
    Toth, IK
    Duncan, JM
    EUROPEAN JOURNAL OF PLANT PATHOLOGY, 2001, 107 (04) : 387 - 398
  • [29] DETECTION OF RHIZOCTONIA CEREALIS IN WHEAT TISSUES BY A REAL-TIME PCR ASSAY
    Hamada, M. S.
    Yin, Y. N.
    Ma, Z. H.
    JOURNAL OF PLANT PATHOLOGY, 2012, 94 (01) : 215 - 217
  • [30] Rapid detection of diarrheagenic E. coli by real-time PCR
    Bischoff, C
    Lüthy, J
    Altwegg, M
    Baggi, F
    JOURNAL OF MICROBIOLOGICAL METHODS, 2005, 61 (03) : 335 - 341