Detailed Information on Publication Record
2016
Competitive Upconversion-Linked Immunosorbent Assay for the Sensitive Detection of Diclofenac
HLAVÁČEK, Antonín, Zdeněk FARKA, Maria HUEBNER, Veronika HORŇÁKOVÁ, Daniel NĚMEČEK et. al.Basic information
Original name
Competitive Upconversion-Linked Immunosorbent Assay for the Sensitive Detection of Diclofenac
Authors
HLAVÁČEK, Antonín (203 Czech Republic, belonging to the institution), Zdeněk FARKA (203 Czech Republic, belonging to the institution), Maria HUEBNER (276 Germany), Veronika HORŇÁKOVÁ (203 Czech Republic, belonging to the institution), Daniel NĚMEČEK (203 Czech Republic, belonging to the institution), Reinhard NIESSNER (276 Germany), Petr SKLÁDAL (203 Czech Republic, guarantor, belonging to the institution), Dietmar KNOPP (276 Germany) and Hans Heiner GORRIS (276 Germany)
Edition
Analytical Chemistry, Washington, D.C., USA, American Chemical Society, 2016, 0003-2700
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10406 Analytical chemistry
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 6.320
RIV identification code
RIV/00216224:14740/16:00090133
Organization unit
Central European Institute of Technology
UT WoS
000377631000065
Keywords in English
antibody; bioconjugation; diclofenac; immunoassay; pharmaceutical micropollutant; photon-upconversion
Tags
Tags
International impact, Reviewed
Změněno: 15/9/2018 18:49, doc. Mgr. Zdeněk Farka, Ph.D.
Abstract
V originále
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).
Links
ED1.1.00/02.0068, research and development project |
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EE2.3.30.0009, research and development project |
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LD15023, research and development project |
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