4.8 Article

Graphite paper-based bipolar electrode electrochemiluminescence sensing platform

期刊

BIOSENSORS & BIOELECTRONICS
卷 94, 期 -, 页码 47-55

出版社

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2017.02.033

关键词

Bipolar electrode; Electrochemiluminescence; Graphite paper; Immunoassay; Carcinoembryonic antigen

资金

  1. National Natural Science Foundation of China [21575022, 21535003]
  2. National High Technology Research and Development Program (863 Program) of China [2015AA020502]
  3. Fundamental Research Funds for the Central Universities [3207046422]
  4. Qing Lan Project
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions [1107047002]

向作者/读者索取更多资源

In this work, aiming at the construction of a disposable, wireless, low-cost and sensitive system for bioassay, we report a closed bipolar electrode electrochemiluminescence (BPE-ECL) sensing platform based on graphite paper as BPE for the first time. Graphite paper is qualified as BPE due to its unique properties such as excellent electrical conductivity, uniform composition and ease of use. This simple BPE-ECL device was applied to the quantitative analysis of oxidant (H2O2) and biomarker (CEA) respectively, according to the principle of BPE sensing-charge balance. For the H2O2 analysis, Pt NPs were electrodeposited onto the cathode through a bipolar electrodeposition approach to promote the sensing performance. As a result, this BPE-ECL device exhibited a wide linear range of 0.001-15 mM with a low detection limit of 0.5 mu M (S/N=3) for H2O2 determination. For the determination of CEA, chitosan-multi-walled carbon nanotubes (CS-MWCNTs) were employed to supply a hydrophilic interface for immobilizing primary antibody (Ab(1)); and Au@Pt nanostructures were conjugated with secondary antibody (Ab(2)) as catalysts for H2O2 reduction. Under the optimal conditions, the BPE-ECL immunodevice showed a wide linear range of 0.01-60 ng mL(-1) with a detection limit of 5.0 pg mL(-1) for CEA. Furthermore, it also displayed satisfactory selectivity, excellent stability and good reproducibility. The developed method opened a new avenue to clinical bioassay.

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