Facile preparation of poly-(styrene-co-maleic anhydride) encapsulated Iridium(III) complexes as highly efficient electrochemiluminescence indicators for sensitive immunoassay of CYFRA 21-1.

Anal Chim Acta

Key Laboratory of Interfacial Reaction & Sensing Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan, 250022, China; Department of Chemistry, Sungkyunkwan University, Suwon, 16419, Republic of Korea. Electronic address:

Published: September 2023

Exploring facile strategy for developing highly efficient emitters using water-insoluble luminophores has become a vital topic in electrochemiluminescence (ECL) immunoassay. In this work, an ECL-active and water-dispersive iridium(III) complex-based polymer dots (IrPdots) was fabricated by encapsulating water-insoluble tris[1-phenylisoquinolinato-C2, N] iridium(III) complexes [Ir(piq)] into poly-(styrene-co-maleic anhydride) (PSMA) matrix by a controllable nanoprecipitation process. The obtained IrPdots generated strong ECL signals in the presence of tri-n-propylamine (TPrA) and were used to label detection antibody (Ab) to act as ECL probes to indicate the signal changes when analyzing target antigen. To construct a sandwich immunosensor, Pd nanoparticles (NPs) decorated MoS/TiCT MXene nanocomposites (MoS/TiCT MXene/Pd) were fabricated as substrates to bind capture antibody (Ab), which could further amplify ECL signals via a coreaction-accelerating pathway to improve the detection sensitivity. When the cytokeratin 19 fragment 21-1 (CYFRA 21-1) was chosen as model analyte, the developed immunosensor displayed a good linear relationship ranging from 0.1 pg/mL to 50 ng/mL with a low detection limit of 95 fg/mL (S/N = 3) was achieved as well. This research proposed a facile and effective method of fabricating IrPdots as ECL probes for immunoassay using water-insoluble iridium complexes, which expanded the application scope of those water-insoluble luminophores for aqueous bioanalysis.

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http://dx.doi.org/10.1016/j.aca.2023.341512DOI Listing

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