Journal
SCIENTIFIC REPORTS
Volume 12, Issue 1, Pages -Publisher
NATURE PORTFOLIO
DOI: 10.1038/s41598-022-13304-z
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Funding
- ENS Paris-Saclay
- CNRS
- Institute Curie
- Institut Pierre-Gilles de Gennes [ANR-10-IDEX-0001-02 PSL, ANR-10-EQPX-34, ANR-10-LABX-31]
- European project FET-OPEN Horizon 2020 INDEX [766466]
- European project FET-OPEN Horizon 2020 CATCH-UDNA [737212]
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This study reports an innovative microfluidic approach using magnetic bead fluidization to directly extract, preconcentrate, and detect IL-6 on a chip. By tuning the physical properties of the beads, assay performance can be improved by enhancing mass transport, reducing non-specific binding, and amplifying the detection signal threefold. By integrating a full ELISA protocol in a single microfluidic chamber, a twofold reduction in LOD and a large dynamic range are achieved.
The cytokine interleukin 6 (IL-6) is involved in the pathogenesis of different inflammatory diseases, including cancer, and its monitoring could help diagnosis, prognosis of relapse-free survival and recurrence. Here, we report an innovative microfluidic approach that uses the fluidization of magnetic beads to specifically extract, preconcentrate and fluorescently detect IL-6 directly on-chip. We assess how the physical properties of the beads can be tuned to improve assay performance by enhancing mass transport, reduce non-specific binding and multiply the detection signal threefold by transitioning between packed and fluidization states. With the integration of a full ELISA protocol in a single microfluidic chamber, we show a twofold reduction in LOD compared to conventional methods along with a large dynamic range (10 pg/mL to 2 ng/mL). We additionally demonstrate its application to IL-6 detection in undiluted serum samples.
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