Competitive Upconversion-Linked Immunosorbent Assay for the Sensitive Detection of Diclofenac
Author(s) -
Antonín Hlaváček,
Zdeněk Farka,
M. Hübner,
Veronika Horňáková,
Daniel Němeček,
Reinhard Nießner,
Petr Skládal,
Dietmar Knopp,
Hans H. Gorris
Publication year - 2016
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/acs.analchem.6b01083
Subject(s) - chemistry , detection limit , photon upconversion , chromatography , immunoassay , conjugated system , drug detection , nanoparticle , analytical chemistry (journal) , nanotechnology , antibody , polymer , organic chemistry , immunology , biology , materials science , ion
Photon-upconverting nanoparticles (UCNPs) emit light of shorter wavelength under near-infrared excitation and thus avoid optical background interference. We have exploited this unique photophysical feature to establish a sensitive competitive immunoassay for the detection of the pharmaceutical micropollutant diclofenac (DCF) in water. The so-called upconversion-linked immunosorbent assay (ULISA) was critically dependent on the design of the upconversion luminescent detection label. Silica-coated UCNPs (50 nm in diameter) exposing carboxyl groups on the surface were conjugated to a secondary anti-IgG antibody. We investigated the structure and monodispersity of the nanoconjugates in detail. Using a highly affine anti-DCF primary antibody, the optimized ULISA reached a detection limit of 0.05 ng DCF per mL. This performance came close to a conventional enzyme-linked immunosorbent assay (ELISA) without the need for an enzyme-mediated signal amplification step. The ULISA was further employed for analyzing drinking and surface water samples. The results were consistent with a conventional ELISA as well as liquid chromatography-mass spectrometry (LC-MS).
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