2024
Single-molecule microfluidic assay for prostate-specific antigen based on magnetic beads and upconversion nanoparticles
SKLENÁROVÁ, Dorota; Antonín HLAVÁČEK; Jana KŘIVÁNKOVÁ; Julian BRANDMEIER; Julie WEISOVÁ et. al.Základní údaje
Originální název
Single-molecule microfluidic assay for prostate-specific antigen based on magnetic beads and upconversion nanoparticles
Autoři
SKLENÁROVÁ, Dorota; Antonín HLAVÁČEK; Jana KŘIVÁNKOVÁ; Julian BRANDMEIER; Julie WEISOVÁ; Michal ŘIHÁČEK; Hans-Heiner GORRIS; Petr SKLÁDAL a Zdeněk FARKA
Vydání
Lab on a Chip, Cambridge, Royal Society of Chemistry, 2024, 1473-0197
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10406 Analytical chemistry
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 5.400
Kód RIV
RIV/00216224:14310/24:00139473
Organizační jednotka
Přírodovědecká fakulta
UT WoS
001258448900001
EID Scopus
2-s2.0-85197932979
Klíčová slova anglicky
Photon-upconversion nanoparticle; Immunoassay; Microfluidics; Prostate-specific antigen
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 4. 4. 2025 13:19, Mgr. Marie Novosadová Šípková, DiS.
Anotace
V originále
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%).
Návaznosti
| GA21-03156S, projekt VaV |
|