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Quantum-dot-based suspension microarray for multiplex detection of lung cancer markers: preclinical validation and comparison with the Luminex xMAP® system

Authors :
Regina Bilan
Amagoia Ametzazurra
Kristina Brazhnik
Sergio Escorza
David Fernández
María Uríbarri
Igor Nabiev
Alyona Sukhanova
The National Research Nuclear University MEPhI (Moscow Engineering Physics Institute) [Moscow, Russia]
Progenika Biopharma SA [Bizkaia, Spain]
Laboratoire de Recherche en Nanosciences - EA 4682 (LRN)
Université de Reims Champagne-Ardenne (URCA)-SFR CAP Santé (Champagne-Ardenne Picardie Santé)
Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-SFR Condorcet
Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)
Source :
Scientific Reports, Scientific Reports, Nature Publishing Group, 2017, 7, pp.44668. ⟨10.1038/srep44668⟩
Publication Year :
2017
Publisher :
Nature Publishing Group, 2017.

Abstract

International audience; A novel suspension multiplex immunoassay for the simultaneous specific detection of lung cancer markers in bronchoalveolar lavage fluid (BALF) clinical samples based on fluorescent microspheres having different size and spectrally encoded with quantum dots (QDEM) was developed. The designed suspension immunoassay was validated for the quantitative detection of three lung cancer markers in BALF samples from 42 lung cancer patients and 10 control subjects. Tumor markers were detected through simultaneous formation of specific immune complexes consisting of a capture molecule, the target antigen, and biotinylated recognition molecule on the surface of the different QDEM in a mixture. The immune complexes were visualized by fluorescently labeled streptavidin and simultaneously analyzed using a flow cytometer. Preclinical validation of the immunoassay was performed and results were compared with those obtained using an alternative 3-plex immunoassay based on Luminex xMAP ® technology, developed on classical organic fluorophores. The comparison showed that the QDEM and xMAP ® assays yielded almost identical results, with clear discrimination between control and clinical samples. Thus, developed QDEM technology can become a good alternative to xMAP ® assays permitting analysis of multiple protein biomarkers using conventional flow cytometers.

Details

Language :
English
ISSN :
20452322
Volume :
7
Database :
OpenAIRE
Journal :
Scientific Reports
Accession number :
edsair.pmid.dedup....7291f9422e5e4980d0d982e778f32d78