Au-coated Fe 3 O 4 core-shell nanohybrids with photothermal activity for point-of-care immunoassay for lipoprotein-associated phospholipase A 2 on a digital near-infrared thermometer

A portable photothermal immunoassay based on Au-coated magnetic Fe O core-shell nanohybrids (Au-Fe O ) was developed for point-of-care (POC) testing of lipoprotein-associated phospholipase A (Lp-PLA ) on a digital near-infrared (NIR) thermometer. Au-Fe O photothermal materials were first synthesized...

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Veröffentlicht in:Analytical and bioanalytical chemistry 2021-01, Vol.413 (1), p.235
Hauptverfasser: Guo, Haixin, Su, Xiaoping, Su, Qingfu, Zhuang, Wei, You, Zhijiao
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Sprache:eng
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Zusammenfassung:A portable photothermal immunoassay based on Au-coated magnetic Fe O core-shell nanohybrids (Au-Fe O ) was developed for point-of-care (POC) testing of lipoprotein-associated phospholipase A (Lp-PLA ) on a digital near-infrared (NIR) thermometer. Au-Fe O photothermal materials were first synthesized through reverse micelle method, and then functionalized with polyclonal rabbit anti-human Lp-PLA antibody. A sandwiched immunoreaction was carried out in polyclonal mouse anti-human Lp-PLA antibody-coated microplate using Au-Fe O -labeled antibody as the detection antibody. With formation of sandwich-type immunocomplex, the captured Au-Fe O on the plate converted the light into heat under an 808-nm laser irradiation (1.5 W cm ), thereby resulting in the increasing temperature of the detection solution. The temperature variations relative to surrounding temperature was determined on a portable NIR thermometer. Several labeling protocols with gold nanoparticle, Fe O nanoparticle, or Au-Fe O nanohybrids were investigated for determination of Lp-PLA and improved analytical features were achieved with the core-shell Au-Fe O nanohybrids. Under optimum conditions, Au-Fe O -based immunoassay exhibited good photothermal responses for the detection of Lp-PLA with a dynamic linear range of 0.01-100 ng mL at a low detection limit of 8.6 pg mL . Good reproducibility and intermediate precision were less than 9.7%. Other biomarkers or proteins did not interfere with responses of this system. An acceptable accuracy was acquired for analysis of human serum sample between Au-Fe O -based photothermal immunoassay and commercialized human Lp-PLA ELISA kit.
ISSN:1618-2650
DOI:10.1007/s00216-020-02995-w