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Microfluidic Digital Immunoassay for Point-of-Care Detection of NT-proBNP from Whole Blood.
Chen, Chao; Porter, Ryan; Zhou, Xiaoyan; Snozek, Christine Lh; Yang, Eric H; Wang, Shaopeng.
Afiliación
  • Chen C; School of Biological and Health Systems Engineering, Arizona State University, Tempe, Arizona 85287, United States.
  • Porter R; Center for Biosensors and Bioelectronics, The Biodesign Institute, Arizona State University, Tempe, Arizona 85287, United States.
  • Zhou X; Center for Biosensors and Bioelectronics, The Biodesign Institute, Arizona State University, Tempe, Arizona 85287, United States.
  • Snozek CL; School of Electrical, Computer and Energy Engineering, Arizona State University, Tempe, Arizona 85287, United States.
  • Yang EH; Center for Biosensors and Bioelectronics, The Biodesign Institute, Arizona State University, Tempe, Arizona 85287, United States.
  • Wang S; School of Electrical, Computer and Energy Engineering, Arizona State University, Tempe, Arizona 85287, United States.
Anal Chem ; 96(26): 10569-10576, 2024 07 02.
Article en En | MEDLINE | ID: mdl-38877973
ABSTRACT
The high prevalence and economic burden of heart failure remain a challenge to global health. This lifelong disease leads to a buildup of permanent heart damage, making early detection and frequent monitoring crucial for effective treatment. N-terminal proBNP (NT-proBNP) is an important biomarker for monitoring the disease state, but current commercial and research NT-proBNP assays require phlebotomy and bulky equipment or do not satisfy clinical requirements such as sensitivity and detection thresholds. Here, we report a point-of-care (POC) compatible microfluidic digital immunoassay that can quantify the NT-proBNP concentration in a small volume of whole blood. Our automated microfluidic device takes whole blood samples mixed with biotinylated detection antibodies and passes through a plasma filter to react with a capture antibody-functionalized sensor surface. Streptavidin-coated gold nanoparticles (GNPs) are then released to mark the surface-bound single NT-proBNP immunocomplexes and recorded with bright-field microscopy. NT-proBNP concentrations in the sample are quantified via a hybrid digital/analog calibration curve. Digital counts of bound GNPs are used as readout signal at low concentrations for high sensitivity detection, and GNP pixel occupancies are used at high concentrations for extended dynamic range. With this approach, we detected NT-proBNP in the range of 8.24-10 000 pg/mL from 7 µL of whole blood in 10 min, with a limit of detection of 0.94 pg/mL. Finally, the method was validated with 15 clinical serum samples, showing excellent linear correlation (r = 0.998) with Roche's Elecsys proBNP II assay. This evidence indicates that this method holds promise for decentralized monitoring of heart failure.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Sistemas de Atención de Punto / Péptido Natriurético Encefálico Límite: Humans Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Sistemas de Atención de Punto / Péptido Natriurético Encefálico Límite: Humans Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos