Paper-based microfluidic electro-analytical device (PMED) for magneto-assay automation: Towards generic point-of-care
J Prat-Trunas1, K Arias-Alpizar1, A Álvarez-Carulla2
1Diagnostic Nanotools Group, Vall d'Hebron Hospital Institut de Recerca (VHIR), Barcelona, Spain; Universitat Autònoma de Barcelona (UAB), Bellaterra, Spain.
This study introduces a novel paper-based microfluidic electro-analytical device (PMED) technology for point-of-care (POC) infectious disease diagnostics. The versatile PMEDs offer quantitative, objective, and cost-effective results, overcoming limitations of current rapid diagnostic tests (RDTs).
Area of Science:
- Biomedical Engineering
- Analytical Chemistry
- Point-of-Care Diagnostics
Background:
- Rapid diagnostic tests (RDTs) are widely used for point-of-care (POC) testing due to their ease of use.
- However, RDTs suffer from limitations including low sensitivity, subjective visual interpretation, batch variability, and poor storage stability.
- Existing RDTs are typically paper-bound, limiting their analytical capabilities and quantitative accuracy.
Purpose of the Study:
- To develop a versatile and cost-effective technology for point-of-care (POC) infectious disease diagnostics.
- To overcome the limitations of traditional rapid diagnostic tests (RDTs) by providing quantitative and objective results.
- To demonstrate the application of the developed technology for detecting specific biomarkers, including Plasmodium falciparum lactate dehydrogenase (Pf-LDH).
Main Methods:
- Development of inexpensive paper-based microfluidic electro-analytical devices (PMEDs) using locally sourced, low-cost equipment.
- Integration of short magneto-assays with PMEDs for analyte detection.
- Utilized commercial or customized screen-printed electrodes and measurement equipment for quantitative analysis.
Main Results:
- PMEDs demonstrated room temperature stability, ease of use, and provided quantitative, objective results.
- The technology successfully quantified streptavidin-HRP, biotinylated HRP, and Plasmodium falciparum lactate dehydrogenase (Pf-LDH) within 25 minutes.
- Pf-LDH detection in diluted whole blood showed a linear response (3-25 ng/mL), with low detection and quantification limits, correlating well with ELISA reference methods.
Conclusions:
- The developed PMED technology offers a versatile, simple, and highly cost-effective solution for point-of-care (POC) testing.
- This technology addresses key limitations of traditional RDTs, enabling accurate and objective disease diagnosis.
- PMEDs hold significant potential for improving infectious disease diagnostics in resource-limited settings.
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