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Disposable silicon-based all-in-one micro-qPCR for rapid on-site detection of pathogens.
Nunez-Bajo, Estefania; Silva Pinto Collins, Alexander; Kasimatis, Michael; Cotur, Yasin; Asfour, Tarek; Tanriverdi, Ugur; Grell, Max; Kaisti, Matti; Senesi, Guglielmo; Stevenson, Karen; Güder, Firat.
Afiliação
  • Nunez-Bajo E; Department of Bioengineering, Imperial College London, London, SW7 2AZ, UK.
  • Silva Pinto Collins A; Department of Bioengineering, Imperial College London, London, SW7 2AZ, UK.
  • Kasimatis M; Department of Bioengineering, Imperial College London, London, SW7 2AZ, UK.
  • Cotur Y; Department of Bioengineering, Imperial College London, London, SW7 2AZ, UK.
  • Asfour T; Department of Bioengineering, Imperial College London, London, SW7 2AZ, UK.
  • Tanriverdi U; Department of Bioengineering, Imperial College London, London, SW7 2AZ, UK.
  • Grell M; Department of Bioengineering, Imperial College London, London, SW7 2AZ, UK.
  • Kaisti M; Department of Bioengineering, Imperial College London, London, SW7 2AZ, UK.
  • Senesi G; Department of Future Technologies, University of Turku, 20500, Turku, Finland.
  • Stevenson K; Department of Bioengineering, Imperial College London, London, SW7 2AZ, UK.
  • Güder F; Moredun Research Institute, Pentlands Science Park, Bush Loan, Edinburgh, Scotland, EH26 0PZ, UK.
Nat Commun ; 11(1): 6176, 2020 12 02.
Article em En | MEDLINE | ID: mdl-33268779
ABSTRACT
Rapid screening and low-cost diagnosis play a crucial role in choosing the correct course of intervention when dealing with highly infectious pathogens. This is especially important if the disease-causing agent has no effective treatment, such as the novel coronavirus SARS-CoV-2, and shows no or similar symptoms to other common infections. Here, we report a disposable silicon-based integrated Point-of-Need transducer (TriSilix) for real-time quantitative detection of pathogen-specific sequences of nucleic acids. TriSilix can be produced at wafer-scale in a standard laboratory (37 chips of 10 × 10 × 0.65 mm in size can be produced in 7 h, costing ~0.35 USD per device). We are able to quantitatively detect a 563 bp fragment of genomic DNA of Mycobacterium avium subspecies paratuberculosis through real-time PCR with a limit-of-detection of 20 fg, equivalent to a single bacterium, at the 35th cycle. Using TriSilix, we also detect the cDNA from SARS-CoV-2 (1 pg) with high specificity against SARS-CoV (2003).
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Técnicas de Amplificação de Ácido Nucleico / COVID-19 Tipo de estudo: Diagnostic_studies Limite: Animals / Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido País de publicação: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Técnicas de Amplificação de Ácido Nucleico / COVID-19 Tipo de estudo: Diagnostic_studies Limite: Animals / Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido País de publicação: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM