Abstract
A novel electrochemiluminescence (ECL) signal amplified strategy based on self-catalyzed luminol derivative and carbon nanohorn-based hybrid for luminol/H2O2 system was firstly proposed, and applied to fabricate an ultrasensitive ECL immunosensor for the detection of N-terminal pro-brain natriuretic peptides (NT-proBNP). Initially, PdCu nanocubes supported single-walled carbon nanohorns (PdCu@SWCNHs) hybrid was successfully synthesized through a facile one-pot strategy. For signal tag fabrication, 3,4,9,10-perylenetetracarboxylic acid (PTCA) conjugated luminol (PTC-Lu) as a novel self-catalyzed luminescence emitter was prepared and then effectively immobilized on the PdCu@SWCNHs to form PTC-Lu/PdCu@SWCNHs nanocomposite via π-π stacking. Herein, PTCA was selected and introduced into the luminol/H2O2 ECL system for the first time, which could not only increase the luminescence signal but also remarkably improve the stability and hydrophilicity of pristine SWCNHs. More notably, PdCu@SWCNHs nanohybrid showed superior catalytic activity toward H2O2 that could further amplify the ECL signal of luminol/H2O2 system. Meanwhile, good biocompatibility and high specific surface area of PdCu nanocubes make the composite possess excellent property for immobilization of detection antibody. Based upon above, the proposed “signal on” immunosensor exhibited a wide linear detection range of 0.1pgmL−1 to 25ngmL−1 with a relatively low detection limit of 0.05pgmL−1, and successfully achieved the detection in clinical human serum samples with desirable results.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.