Sample-to-answer lateral flow assay with integrated plasma separation and NT-proBNP detection

• Published in: Analytical and bioanalytical chemistry Vol. 416; no. 13; pp. 3107 - 3115
• Main Authors: Strohmaier-Nguyen, Dan, Horn, Carina, Baeumner, Antje J.
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.05.2024; Springer Nature B.V
• Subjects: Agglutination; Analytical Chemistry; Antibodies; Biochemistry; Blood; Blood volume; Centrifugation; Characterization and Evaluation of Materials; Chemistry; Chemistry and Materials Science; Control systems; Dilution; Equipment Design; Erythrocytes; Fluorescence; Food Science; Humans; Immunoassay; Immunoassay - instrumentation; Immunoassay - methods; Laboratory Medicine; Monitoring/Environmental Analysis; Natriuretic Peptide, Brain - blood; Natriuretic Peptide, Brain - isolation & purification; Paper in Forefront; Peptide Fragments - blood; Plasma; Point-of-Care Testing; Polymers; Rehydration; Sedimentation; Separation; Streptavidin; Suction; Point-of-care diagnostics; Lateral flow assay; Blood plasma separation; Sample-to-answer; Sedimentation
• ISSN: 1618-2642; 1618-2650
• DOI: 10.1007/s00216-024-05271-3

Through enabling whole blood detection in point-of-care testing (POCT), sedimentation-based plasma separation promises to enhance the functionality and extend the application range of lateral flow assays (LFAs). To streamline the entire process from the introduction of the blood sample to the generation of quantitative immune-fluorescence results, we combined a simple plasma separation technique, an immunoreaction, and a micropump-driven external suction control system in a polymer channel-based LFA. Our primary objective was to eliminate the reliance on sample-absorbing separation membranes, the use of active separation forces commonly found in POCT, and ultimately allowing finger prick testing. Combining the principle of agglutination of red blood cells with an on-device sedimentation-based separation, our device allows for the efficient and fast separation of plasma from a 25-µL blood volume within a mere 10 min and overcomes limitations such as clogging, analyte adsorption, and blood pre-dilution. To simplify this process, we stored the agglutination agent in a dried state on the test and incorporated a filter trench to initiate sedimentation-based separation. The separated plasma was then moved to the integrated mixing area, initiating the immunoreaction by rehydration of probe-specific fluorophore-conjugated antibodies. The biotinylated immune complex was subsequently trapped in the streptavidin-rich detection zone and quantitatively analyzed using a fluorescence microscope. Normalized to the centrifugation-based separation, our device demonstrated high separation efficiency of 96% and a yield of 7.23 µL (= 72%). Furthermore, we elaborate on its user-friendly nature and demonstrate its proof-of-concept through an all-dried ready-to-go NT-proBNP lateral flow immunoassay with clinical blood samples. Graphical Abstract