Issue 14, 2024

Single-molecule microfluidic assay for prostate-specific antigen based on magnetic beads and upconversion nanoparticles

Abstract

Early-stage diagnosis of prostatic carcinoma is essential for successful treatment and, thus, significant prognosis improvement. In laboratory practice, the standard non-invasive diagnostic approach is the immunochemical detection of the associated biomarker, prostate-specific antigen (PSA). Ultrasensitive detection of PSA is essential for both diagnostic and recurrence monitoring purposes. To achieve exceptional sensitivity, we have developed a microfluidic device with a flow-through cell for single-molecule analysis using photon-upconversion nanoparticles (UCNPs) as a detection label. For this purpose, magnetic microparticles (MBs) were first optimized for the capture and preconcentration of PSA and then used to implement a bead-based upconversion-linked immunoassay (ULISA) in the microfluidic device. The digital readout based on counting single nanoparticle-labeled PSA molecules on MBs enabled a detection limit of 1.04 pg mL−1 (36 fM) in 50% fetal bovine serum, which is an 11-fold improvement over the respective analog MB-based ULISA. The microfluidic technique conferred several other advantages, such as easy implementation and the potential for achieving high-throughput analysis. Finally, it was proven that the microfluidic setup is suitable for clinical sample analysis, showing a good correlation with a reference electrochemiluminescence assay (recovery rates between 97% and 105%).

Graphical abstract: Single-molecule microfluidic assay for prostate-specific antigen based on magnetic beads and upconversion nanoparticles

Supplementary files

Article information

Article type
Paper
Submitted
22 Apr 2024
Accepted
23 Jun 2024
First published
24 Jun 2024
This article is Open Access
Creative Commons BY license

Lab Chip, 2024,24, 3536-3545

Single-molecule microfluidic assay for prostate-specific antigen based on magnetic beads and upconversion nanoparticles

D. Sklenárová, A. Hlaváček, J. Křivánková, J. C. Brandmeier, J. Weisová, M. Řiháček, H. H. Gorris, P. Skládal and Z. Farka, Lab Chip, 2024, 24, 3536 DOI: 10.1039/D4LC00346B

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