4.7 Article

Multi-function PtCo nanozymes/CdS nanocrystals@graphene oxide luminophores and K2S2O8/H2O2 coreactants-based dual amplified electrochemiluminescence immunosensor for ultrasensitive detection of anti-myeloperoxidase antibody

期刊

JOURNAL OF NANOBIOTECHNOLOGY
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12951-021-00968-4

关键词

PtCo/CdS@GO luminophores; Nanozyme; K2S2O8/H2O2 coreactants; Electrochemiluminescence immunosensor; Anti-myeloperoxidase antibody

资金

  1. National Science and Technology Major Project of the Ministry of Science and Technology of China [2018ZX10732202]
  2. Zhejiang Public Welfare Technology Application Research Project [2017C33091]
  3. Zhejiang Provincial Natural Science Fund [LQ21H200005]

向作者/读者索取更多资源

A dual amplified electrochemiluminescence immunosensor was developed for ultrasensitive detection of anti-MPO, using PtCo/CdS@GO luminophores and K2S2O8/H2O2 coreactants. The novel signal amplification labels demonstrated excellent peroxidase-like catalytic activity and high-efficiency luminescence performance, leading to a low detection limit and good concentration linearity for anti-MPO detection. This study not only successfully detected anti-MPO in clinical serum samples, but also provided a new concept for designing high-performance luminophores with wide potential for biomarkers detection in clinical diagnosis.
Background: Anti-myeloperoxidase antibody (anti-MPO) is an important biomarker for anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitides (AAVs). However, the complicated operation procedures and insufficient sensitivity of conventional anti-MPO detection methods limit their application in monitoring efficacy of AAVs in clinical diagnosis. Herein, a dual amplified electrochemiluminescence (ECL) immunosensor based on multi-function PtCo nanozymes/CdS nanocrystals@graphene oxide (PtCo/CdS@GO) luminophores and K2S2O8/H2O2 coreactants has been fabricated for ultrasensitive detection of anti-MPO. Results: PtCo/CdS@GO luminophores as novel signal amplification labels and nanocarriers to load rabbit anti-mouse IgG were synthesized by co-doping with Pt and Co nanozymes simultaneously with several considerable advantages, including astonishing peroxidase-like catalytic activity, high-efficiency luminescence performance and superior stability in aqueous solutions. Meanwhile, upon the K2S2O8/H2O2 coreactants system, benefiting from the efficient peroxidase-like activity of the PtCo/CdS@GO toward H2O2, massive of transient reactive intermediates could react with K2S2O8, thus obtaining higher ECL emission. Therefore, the developed ECL immunosensor for anti-MPO detection displayed good analytical performance with good concentration linearity in the range of 0.02 to 1000 pg/mL and low detection limit down to 7.39 fg/mL. Conclusions: The introduction of multi-function PtCo/CdS@GO luminophores into the established ECL immunoassay not only was successfully applied for specific detection of anti-MPO in clinical serum samples, but also provided a completely new concept to design other high-performance luminophores. Meaningfully, the ECL immunoassay strategy held wide potential for biomarkers detection in clinical diagnosis.

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