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All-fiber all-optical quantitative polymerase chain reaction (qPCR).
Li, Xuegang; Nguyen, Linh V; Hill, Kelly; Ebendorff-Heidepriem, Heike; Schartner, Erik P; Zhao, Yong; Zhou, Xue; Zhang, Yanan; Warren-Smith, Stephen C.
Afiliação
  • Li X; College of Information Science and Engineering, Northeastern University, Shenyang, Liaoning, 110819, China.
  • Nguyen LV; Institute for Photonics and Advanced Sensing and School of Physical Sciences, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Hill K; Institute for Photonics and Advanced Sensing and School of Physical Sciences, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Ebendorff-Heidepriem H; South Australian Research and Development Institute, Urrbrae, SA, 5064, Australia.
  • Schartner EP; School of Agriculture, Food and Wine, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Zhao Y; Institute for Photonics and Advanced Sensing and School of Physical Sciences, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Zhou X; ARC Centre of Excellence for Nanoscale BioPhotonics, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Zhang Y; Institute for Photonics and Advanced Sensing and School of Physical Sciences, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Warren-Smith SC; ARC Centre of Excellence for Nanoscale BioPhotonics, The University of Adelaide, Adelaide, SA, 5005, Australia.
Sens Actuators B Chem ; 323: 128681, 2020 Nov 15.
Article em En | MEDLINE | ID: mdl-32834504
Quantitative polymerase chain reaction (qPCR), the real-time amplification and measurement of a targeted DNA molecule, has revolutionized the biological sciences and is routinely applied in areas such as medical diagnostics, forensics, and agriculture. Despite widescale use of qPCR technology in the lab, the availability of low-cost and high-speed portable systems remains one of the barriers to routine in-field implementation. Here we propose and demonstrate a potential solution using a photonics-based qPCR system. By using an all-optical approach, we achieve ultra-fast temperature response with real-time temperature feedback using nanoliter scale reaction volumes. The system uses a microcavity to act as a nanoliter scale reaction vessel with a laser-driven and optically monitored temperature cycling system for ultrafast thermal cycling and incorporates an all-fiber fluorescence excitation/detection system to achieve real-time, high sensitivity fluorescence monitoring of the qPCR process. Further, we demonstrate the potential of the system to operate as a label-free qPCR system through direct optical measurement of the sample refractive index. Due to advantages in portability and fabrication simplicity, we anticipate that this platform technology will offer a new strategy for fundamental techniques in biochemistry applications, such as point-of-care and remote diagnostics.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sens Actuators B Chem Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sens Actuators B Chem Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China