A low-cost PCR instrument for molecular disease diagnostics based on customized printed circuit board heaters.

This article describes the fabrication of a low-cost Polymerase Chain Reaction (PCR) instrument to detect diseases. In order to reduce the instrument price and simplify construction we developed an alternative fabrication process, transforming conventional printed circuit boards (PCB) in heating ele...

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Publicado en:Biomedical Microdevices Vol. 23; no. 2; pp. 1 - 9
Autores principales: de Oliveira, Viviane Klassen, Camargo, Bruno Dias, Alexandrino, Fabiana, Morello, Luis Gustavo, Marchini, Fabricio Klerynton, Aoki, Mateus Nóbrega, Blanes, Lucas
Formato: Journal Article
Publicado: Springer Nature Jun2021
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jun2021
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s10544-021-00563-2
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        atl: A low-cost PCR instrument for molecular disease diagnostics based on customized printed circuit board heaters.
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          de Oliveira, Viviane Klassen
          Camargo, Bruno Dias
          Alexandrino, Fabiana
          Morello, Luis Gustavo
          Marchini, Fabricio Klerynton
          Aoki, Mateus Nóbrega
          Blanes, Lucas
        affil: Laboratory for Applied Science and Technology in Health, Carlos Chagas Institute, Oswaldo Cruz Foundation (Fiocruz), Curitiba, Brazil
      sug:
      ab: This article describes the fabrication of a low-cost Polymerase Chain Reaction (PCR) instrument to detect diseases. In order to reduce the instrument price and simplify construction we developed an alternative fabrication process, transforming conventional printed circuit boards (PCB) in heating elements, avoiding the use of aluminum heating/cooling blocks and Peltier devices. To cool down the reaction a simple computer fan was used. The vial holder was fabricated using two double side PCB boards assembled in a sandwich-like configuration. The bottom PCB has a resistance of 0.9 Ω used to heat the reaction mix, while the top layer has a resistance of 1.1 Ω to heat the vial body, preventing vapor condensation. The top board was maintained at ~ 110 ± 1 °C during all cycles. The final device was able to heat and cool down the reaction at rates of ~ 2.0 °C/s, a rate comparable to commercial thermocyclers. An SMD NTC thermistor was used as temperature sensors, and a PID (proportional–integral–derivative) control algorithm was implemented to acquire and precisely control the temperature. We also discuss how the instrument is calibrated. The device was tested successfully for the amplification of T. pallidum (Syphilis) bacterial DNA and Zika virus RNA samples, showing similar performance to a commercial PCR instrument.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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