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Peer-reviewedCC BY-NC-ND 4.0Scientific Reports

Microfluidic platform for rapid passive preparation of complex biological matrices in point-of-care testing

  1. 1Department of Biology, York University, 4700 Keele Street, Toronto, ON M3J 1P3 Canada
  2. 2Laboratory of Advanced Biotechnologies for Health Assessments (Lab-HA), Lassonde School of Engineering, York University, Toronto, ON M3J 1P3 Canada
  3. 3Department of Electrical Engineering and Computer Science (EECS), Lassonde School of Engineering, York University, Toronto, ON M3J 1P3 Canada

Abstract

Efficient whole blood processing at the point-of-care (POC) remains challenging due to interference from cellular components, risk of hemolysis, as well as reliance on external equipment and skilled operators. Here, we present a passive, low-cost microfluidic platform for rapid separation of cellular components from diluted samples of whole blood without the need for external pumps. The device features a circular maze-shaped microchannel incorporating 18 sequential wells, enabling effective cell retention through purely passive hydrodynamic mechanisms. Fabricated from hydrophilic polymer sheets and pressure-sensitive adhesive (PSA) layers, the platform is scalable, disposable, and enables very low-cost production (< $1 per unit). The blood-separation performance of the standalone microfluidic chip was validated using HEK-293 and AtT-20 cell suspensions, mixed cell suspensions, and diluted human blood. Efficient retention of cellular components in the early wells generated a cell-free filtrate suitable for downstream analytical applications. Building on this validated separation capability, the platform was integrated with a lateral flow immunoassay (LFIA) module as a proof-of-concept in a POC application by testing for hepatitis B surface antigen (HBsAg). The integrated system enabled detection of HBsAg at concentrations as low as 10 ng/mL within 10 min. In addition, deep learning–assisted convolutional neural networks were employed for automated assessment of filtration efficiency and test-line intensity. Overall, this work demonstrates a robust and accessible microfluidic sample-preparation platform with potential for decentralized diagnostic applications, particularly critical for resource-limited settings.

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BibTeX
@article{sadighbayan2026microfluidic,
  title = {{Microfluidic platform for rapid passive preparation of complex biological matrices in point-of-care testing}},
  author = {Deniz Sadighbayan and Alireza Norouziazad and Fatemeh Rahimi and Jean-Paul Paluzzi and Razieh Salahandish},
  journal = {Scientific Reports},
  year = {2026},
  month = jul,
  doi = {10.1038/s41598-026-63706-6},
  url = {https://doi.org/10.1038/s41598-026-63706-6},
  note = {CC BY-NC-ND 4.0},
}
RIS
TY  - JOUR
TI  - Microfluidic platform for rapid passive preparation of complex biological matrices in point-of-care testing
AU  - Deniz Sadighbayan
AU  - Alireza Norouziazad
AU  - Fatemeh Rahimi
AU  - Jean-Paul Paluzzi
AU  - Razieh Salahandish
PY  - 2026
DA  - 2026/07/28
JO  - Scientific Reports
DO  - 10.1038/s41598-026-63706-6
UR  - https://doi.org/10.1038/s41598-026-63706-6
AB  - Efficient whole blood processing at the point-of-care (POC) remains challenging due to interference from cellular components, risk of hemolysis, as well as reliance on external equipment and skilled operators. Here, we present a passive, low-cost microfluidic platform for rapid separation of cellular components from diluted samples of whole blood without the need for external pumps. The device features a circular maze-shaped microchannel incorporating 18 sequential wells, enabling effective cell retention through purely passive hydrodynamic mechanisms. Fabricated from hydrophilic polymer sheets and pressure-sensitive adhesive (PSA) layers, the platform is scalable, disposable, and enables very low-cost production (< $1 per unit). The blood-separation performance of the standalone microfluidic chip was validated using HEK-293 and AtT-20 cell suspensions, mixed cell suspensions, and diluted human blood. Efficient retention of cellular components in the early wells generated a cell-free filtrate suitable for downstream analytical applications. Building on this validated separation capability, the platform was integrated with a lateral flow immunoassay (LFIA) module as a proof-of-concept in a POC application by testing for hepatitis B surface antigen (HBsAg). The integrated system enabled detection of HBsAg at concentrations as low as 10 ng/mL within 10 min. In addition, deep learning–assisted convolutional neural networks were employed for automated assessment of filtration efficiency and test-line intensity. Overall, this work demonstrates a robust and accessible microfluidic sample-preparation platform with potential for decentralized diagnostic applications, particularly critical for resource-limited settings.
SN  - 2045-2322
ER  -