Integrated acoustic immunoaffinity-capture (IAI) platform for detection of PSA from whole blood samplesConflict of interest: Dr Hans Lilja holds patents for free PSA, hK2 and intact PSA assays

On-chip detection of low abundant protein biomarkers is of interest to enable point-of-care diagnostics. Using a simple form of integration, we have realized an integrated microfluidic platform for the detection of prostate specific antigen (PSA), directly in anti-coagulated whole blood. We combine...

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Hauptverfasser: Tajudin, A. Ahmad, Petersson, K, Lenshof, A, Swärd-Nilsson, A.-M, Åberg, L, Marko-Varga, G, Malm, J, Lilja, H, Laurell, T
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Sprache:eng
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Zusammenfassung:On-chip detection of low abundant protein biomarkers is of interest to enable point-of-care diagnostics. Using a simple form of integration, we have realized an integrated microfluidic platform for the detection of prostate specific antigen (PSA), directly in anti-coagulated whole blood. We combine acoustophoresis-based separation of plasma from undiluted whole blood with a miniaturized immunoassay system in a polymer manifold, demonstrating improved assay speed on our Integrated Acoustic Immunoaffinity-capture (IAI) platform. The IAI platform separates plasma from undiluted whole blood by means of acoustophoresis and provides cell free plasma of clinical quality at a rate of 10 uL/min for an online immunoaffinity-capture of PSA on a porous silicon antibody microarray. The whole blood input (hematocrit 38-40%) rate was 50 μl min −1 giving a plasma volume fraction yield of 33%. PSA was immunoaffinity-captured directly from spiked female whole blood samples at clinically significant levels of 1.7-100 ng ml −1 within 15 min and was subsequently detected via fluorescence readout, showing a linear response over the entire range with a coefficient of variation of 13%. We present an integrated microfluidic platform for the detection of prostate specific antigen (PSA), directly in anti-coagulated whole blood.
ISSN:1473-0197
1473-0189
DOI:10.1039/c3lc41269e