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Magnetic Bead Handling Using a Paper-Based Device for Quantitative Point-of-Care Testing.

Kevin Arias-Alpízar1,2, Ana Sánchez-Cano1,2, Judit Prat-Trunas1

  • 1Diagnostic Nanotools Group, Vall d'Hebron Institut de Recerca (VHIR), 08035 Barcelona, Spain.

Biosensors
|September 23, 2022
PubMed
Summary
This summary is machine-generated.

This study introduces a novel microfluidic paper-based analytical device (μPAD) for rapid malaria diagnosis. The affordable μPAD automates a magneto-immunoassay, enabling sensitive Plasmodium falciparum lactate dehydrogenase (Pf-LDH) detection at room temperature.

Keywords:
immuno-modified magnetic beadslow-cost assay automationmalaria quantitative diagnosispaper-based diagnostic devicepoint-of-care testingsmartphone colorimetric detection

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Area of Science:

  • Analytical Chemistry
  • Biomedical Engineering
  • Point-of-Care Diagnostics

Background:

  • Microfluidic paper-based analytical devices (μPADs) offer potential for point-of-care (POC) testing.
  • Existing μPADs often rely on dried reagents, leading to production, stability, and storage challenges.
  • Room temperature storage and simplified manufacturing are critical for widespread POC adoption.

Purpose of the Study:

  • To develop an affordable, room-temperature-storable μPAD for partially automating magneto-immunoassays.
  • To demonstrate the μPAD's utility for quantitative detection of Plasmodium falciparum lactate dehydrogenase (Pf-LDH), a malaria biomarker.
  • To assess the device's performance against established diagnostic methods.

Main Methods:

  • Fabrication of μPADs using a craft cutter for affordability and ease of production.
  • Implementation of a single-step colorimetric magneto-immunoassay involving magnetic beads (MB), antibodies, and an enzymatic amplifier.
  • On-chip magnetic concentration and washing of MBs, followed by colorimetric signal generation and readout via naked eye or smartphone imaging.

Main Results:

  • Quantitative detection of Pf-LDH achieved in under 15 minutes.
  • Detection limits of 6.25 ng mL−1 (naked eye) and 1.4 ng mL−1 (smartphone imaging).
  • Clinical sample analysis showed correlation with ELISA and superior sensitivity compared to commercial rapid diagnostic tests (RDTs).

Conclusions:

  • The developed μPAD enables partial automation of magneto-immunoassays, meeting key requirements for POC testing.
  • The device offers a stable, room-temperature-storable, and affordable platform for malaria diagnosis.
  • This approach significantly enhances the potential of μPADs for accessible and sensitive disease detection.