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Nucleic acid sample preparation from whole blood in a paper microfluidic device using isotachophoresis.
Sullivan, Benjamin P; Bender, Andrew T; Ngyuen, Duy N; Zhang, Jane Yuqian; Posner, Jonathan D.
Afiliação
  • Sullivan BP; Department of Mechanical Engineering, University of Washington, Seattle, WA, USA.
  • Bender AT; Department of Mechanical Engineering, University of Washington, Seattle, WA, USA.
  • Ngyuen DN; Department of Chemical Engineering, University of Washington, Seattle, WA, USA.
  • Zhang JY; Department of Mechanical Engineering, University of Washington, Seattle, WA, USA.
  • Posner JD; Department of Mechanical Engineering, University of Washington, Seattle, WA, USA; Department of Chemical Engineering, University of Washington, Seattle, WA, USA; Department of Family Medicine, University of Washington, Seattle, WA, USA. Electronic address: jposner@uw.edu.
Article em En | MEDLINE | ID: mdl-33401049
ABSTRACT
Nucleic acid amplification tests (NAATs) are a crucial diagnostic and monitoring tool for infectious diseases. A key procedural step for NAATs is sample preparation separating and purifying target nucleic acids from crude biological samples prior to nucleic acid amplification and detection. Traditionally, sample preparation has been performed with liquid- or solid-phase extraction, both of which require multiple trained user steps and significant laboratory equipment. The challenges associated with sample preparation have limited the dissemination of NAAT point-of-care diagnostics in low resource environments, including low- and middle-income countries. We report on a paper-based device for purification of nucleic acids from whole blood using isotachophoresis (ITP) for point-of-care NAATs. We show successful extraction and purification of target nucleic acids from large volumes (33 µL) of whole human blood samples with no moving parts and few user steps. Our device utilizes paper-based buffer reservoirs to fully contain the liquid ITP buffers and does not require complex filling procedures, instead relying on the natural wicking of integrated paper membranes. We perform on-device blood fractionation via filtration to remove leukocytes and erythrocytes from our sample, followed by integrated on-paper proteolytic digestion of endogenous plasma proteins to allow for successful isotachophoretic extraction. Paper-based isotachophoresis purifies and concentrates target nucleic acids that are added directly to recombinase polymerase amplification (RPA) reactions. We show consistent amplification of input copy concentrations of as low as 3 × 103 copies nucleic acid per mL input blood with extraction and purification taking only 30 min. By employing a paper architecture, we are able to incorporate these processes in a single, robust, low-cost design, enabling the direct processing of large volumes of blood, with the only intermediate user steps being the removal and addition of tape. Our device represents a step towards a simple, fully integrated sample preparation system for nucleic acid amplification tests at the point-of-care.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Nucleicos / Técnicas Analíticas Microfluídicas / Dispositivos Lab-On-A-Chip / Isotacoforese Limite: Humans Idioma: En Revista: J Chromatogr B Analyt Technol Biomed Life Sci Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Nucleicos / Técnicas Analíticas Microfluídicas / Dispositivos Lab-On-A-Chip / Isotacoforese Limite: Humans Idioma: En Revista: J Chromatogr B Analyt Technol Biomed Life Sci Ano de publicação: 2021 Tipo de documento: Article