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Toward one-step point-of-care immunodiagnostics using capillary-driven microfluidics and PDMS substrates
Luc Gervais1, Emmanuel Delamarche
1University Hospital Basel, Petersgraben 4, 4031, Basel, Switzerland.
This study introduces a novel one-step microfluidic immunoassay chip for rapid point-of-care diagnostics. The device integrates reagents and uses capillary forces for sensitive detection of C-reactive protein (CRP) in human serum.
Area of Science:
- Biomedical Engineering
- Analytical Chemistry
- Diagnostics
Background:
- Microfluidics offers significant advantages for point-of-care diagnostics, including sample preservation, enhanced sensitivity, and faster reaction times.
- A key challenge in microfluidic diagnostics is the integration of reagents and user-friendliness for rapid assays.
Purpose of the Study:
- To develop and validate a novel one-step microfluidic immunoassay for point-of-care diagnostics.
- To integrate essential reagents and microfluidic elements for a capillary-driven, sandwich immunoassay.
Main Methods:
- Integration of microfluidic components including a sample collector, delay valves, flow resistors, and a reaction chamber sealed with a patterned polydimethylsiloxane (PDMS) substrate.
- Optimization of inkjet deposition of detection antibodies (dAbs) and patterning of capture antibodies (cAbs) and analytes on PDMS.
- Detection of C-reactive protein (CRP) in human serum using capillary forces and fluorescence microscopy.
Main Results:
- The developed one-step microfluidic chip successfully detected CRP in 5 microL of human serum.
- Detection limits for CRP were achieved at 10 ng/mL in under 3 minutes and below 1 ng/mL within 14 minutes.
- Storage of patterned PDMS with desiccant maintained over 51% of capture antibody activity for up to 6 months.
Conclusions:
- This integrated microfluidic device enables a simple, one-step fluorescence immunoassay for point-of-care applications.
- The capillary-driven microfluidic system demonstrates potential for rapid and sensitive detection of biomarkers like CRP.
- The findings may promote the use of microfluidics and PDMS substrates in fluorescence immunoassays for diagnostics.
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