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Gravity-Driven Microfluidic Siphons: Fluidic Characterization and Application to Quantitative Immunoassays.
Reis, Nuno M; Needs, Sarah H; Jegouic, Sophie M; Gill, Kirandeep K; Sirivisoot, Sirintra; Howard, Scott; Kempe, Jack; Bola, Shaan; Al-Hakeem, Kareem; Jones, Ian M; Prommool, Tanapan; Luangaram, Prasit; Avirutnan, Panisadee; Puttikhunt, Chunya; Edwards, Alexander D.
  • Reis NM; Department of Chemical Engineering and Centre for Biosensors, Biodevices and Bioelectronics (C3Bio), University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
  • Needs SH; Reading School of Pharmacy, University of Reading, Whiteknights Campus, Reading, RG6 6AD United Kingdom.
  • Jegouic SM; Reading School of Pharmacy, University of Reading, Whiteknights Campus, Reading, RG6 6AD United Kingdom.
  • Gill KK; School of Biological Sciences, University of Reading, Whiteknights Campus, Reading, RG6 6AJ, United Kingdom.
  • Sirivisoot S; Department of Chemical Engineering and Centre for Biosensors, Biodevices and Bioelectronics (C3Bio), University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
  • Howard S; Dengue Hemorrhagic Fever Research Unit, Office for Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand.
  • Kempe J; Department of Chemical Engineering and Centre for Biosensors, Biodevices and Bioelectronics (C3Bio), University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
  • Bola S; Department of Chemical Engineering and Centre for Biosensors, Biodevices and Bioelectronics (C3Bio), University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
  • Al-Hakeem K; Department of Chemical Engineering and Centre for Biosensors, Biodevices and Bioelectronics (C3Bio), University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
  • Jones IM; Department of Chemical Engineering and Centre for Biosensors, Biodevices and Bioelectronics (C3Bio), University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
  • Prommool T; School of Biological Sciences, University of Reading, Whiteknights Campus, Reading, RG6 6AJ, United Kingdom.
  • Luangaram P; Molecular Biology of Dengue and Flaviviruses Research Team, Medical Molecular Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathum Thani, 73170, Thailand.
  • Avirutnan P; Molecular Biology of Dengue and Flaviviruses Research Team, Medical Molecular Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathum Thani, 73170, Thailand.
  • Puttikhunt C; Dengue Hemorrhagic Fever Research Unit, Office for Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand.
  • Edwards AD; Molecular Biology of Dengue and Flaviviruses Research Team, Medical Molecular Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathum Thani, 73170, Thailand.
ACS Sens ; 6(12): 4338-4348, 2021 12 24.
Article in English | MEDLINE | ID: covidwho-1545581
ABSTRACT
A range of biosensing techniques including immunoassays are routinely used for quantitation of analytes in biological samples and available in a range of formats, from centralized lab testing (e.g., microplate enzyme-linked immunosorbent assay (ELISA)) to automated point-of-care (POC) and lateral flow immunochromatographic tests. High analytical performance is intrinsically linked to the use of a sequence of reagent and washing steps, yet this is extremely challenging to deliver at the POC without a high level of fluidic control involving, e.g., automation, fluidic pumping, or manual fluid handling/pipetting. Here we introduce a microfluidic siphon concept that conceptualizes a multistep ″dipstick″ for quantitative, enzymatically amplified immunoassays using a strip of microporous or microbored material. We demonstrated that gravity-driven siphon flow can be realized in single-bore glass capillaries, a multibored microcapillary film, and a glass fiber porous membrane. In contrast to other POC devices proposed to date, the operation of the siphon is only dependent on the hydrostatic liquid pressure (gravity) and not capillary forces, and the unique stepwise approach to the delivery of the sample and immunoassay reagents results in zero dead volume in the device, no reagent overlap or carryover, and full start/stop fluid control. We demonstrated applications of a 10-bore microfluidic siphon as a portable ELISA system without compromised quantitative capabilities in two global diagnostic applications (1) a four-plex sandwich ELISA for rapid smartphone dengue serotype identification by serotype-specific dengue virus NS1 antigen detection, relevant for acute dengue fever diagnosis, and (2) quantitation of anti-SARS-CoV-2 IgG and IgM titers in spiked serum samples. Diagnostic siphons provide the opportunity for high-performance immunoassay testing outside sophisticated laboratories, meeting the rapidly changing global clinical and public health needs.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Microfluidics / COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: ACS Sens Year: 2021 Document Type: Article Affiliation country: Acssensors.1c01524

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Microfluidics / COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: ACS Sens Year: 2021 Document Type: Article Affiliation country: Acssensors.1c01524