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Related Concept Videos

Enzyme-Linked Immunosorbent Assay01:33

Enzyme-Linked Immunosorbent Assay

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In 1971, Peter Perlman and Eva Engvall developed an Enzyme-linked immunosorbent assay (ELISA or EIA). ELISA differs from western blot in that the assays are conducted in microtiter plates or in vivo rather than on an absorbent membrane.
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen.  Enzyme-substrate reaction allows the antigen to be visualized or...
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Dry Film Photoresist-based Electrochemical Microfluidic Biosensor Platform: Device Fabrication, On-chip Assay Preparation, and System Operation
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Split-Type Electrochemical Immunoassay System Triggering Ascorbic Acid-Mediated Signal Magnification Based on a

Liu Qu1, Xiang Ren1, Dawei Fan1

  • 1Collaborative Innovation Center for Green Chemical Manufacturing and Accurate Detection, Key Laboratory of Interfacial Reaction & Sensing Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan, 250022 Shandong, China.

ACS Applied Materials & Interfaces
|June 8, 2021
PubMed
Summary

A novel electrochemical immunosensor uses a controlled-release strategy for sensitive neuron-specific enolase (NSE) detection. This biosensor integrates ascorbic acid (AA) release with a gold nanoparticle/porous bismuth vanadate platform for signal amplification.

Keywords:
SBGCdS-AAcontrolled-release strategyneuron-specific enolasesplit-type EC immunosensorsynergetic catalysis oxidation

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Area of Science:

  • Electrochemistry
  • Biosensing
  • Nanomaterials

Background:

  • Traditional electrochemical immunosensors face challenges with immune interference and steric hindrance.
  • Developing sensitive and efficient biosensing platforms for disease biomarkers is crucial.

Purpose of the Study:

  • To develop a novel split-type electrochemical immunosensor for sensitive neuron-specific enolase (NSE) detection.
  • To integrate a controlled-release strategy with electrochemical detection to minimize bioanalytical complexity and enhance sensitivity.

Main Methods:

  • Ascorbic acid (AA) was encapsulated in cadmium sulfide-capped spherical mesoporous bioactive glass nanocarriers (SBGCdS).
  • A 96-well microplate was used for antibody-based immunoreactions, separating it from electrochemical detection.
  • AA was released using dithiothreitol, and its oxidation was catalyzed by a FcAI/l-Cys/gold nanoparticles/porous BiVO4/ITO electrochemical sensing platform for signal amplification.

Main Results:

  • The electrochemical immunosensor demonstrated sensitive detection of neuron-specific enolase (NSE).
  • A wide linear range of 0.001-100 ng/mL and a low detection limit of 1.08 pg/mL were achieved.
  • The ordered nanoarray structure of porous BiVO4 accelerated electron transfer, enhancing system sensitivity.

Conclusions:

  • The developed split-type electrochemical immunosensor effectively overcomes limitations of traditional methods.
  • This approach offers a sensitive and reliable method for neuron-specific enolase (NSE) biomarker assay.
  • The study presents an innovative strategy for the bioanalysis of NSE and potentially other biomarkers.