An electrochemiluminescence biosensor based on silver-cysteine nanorod as an emitter and AgNP-decorated FeMoOν as a signal amplifier for sensitive detection of heart-type fatty acid binding protein

Mikrochim Acta. 2024 Dec 30;192(1):46. doi: 10.1007/s00604-024-06923-y.

Abstract

An electrochemiluminescence (ECL) immunosensor was developed for the highly sensitive and specific detection of heart-type fatty acid binding protein (H-FABP) and the rapid diagnosis of acute myocardial infarction (AMI). H-FABP is a biomarker that is highly specific to cardiac tissue and is associated with a range of cardiac diseases. Following myocardial injury, the rate of increase in H-FABP levels is greater than that observed for myoglobin and troponin. Therefore, the measurement of H-FABP is crucial for the early exclusion of AMI. Silver-cysteine nanorod (AgCysNR), which served as the ECL emitter, was produced with a one-step, green, simple, template-free aqueous phase method. The surfaces of AgCysNR displayed many amino and carboxyl groups that were connected to a large number of a secondary H-FABP-specific antibody. Ferrum-doped molybdenum oxide (FeMoOν), with a large specific surface area, was richly decorated with silver nanoparticle (AgNP), which increased the interfacial electron transfer rate of FeMoOν. The AgNP was used as a co-reaction accelerator to promote persulfate to produce more sulfate anion radical and then enhance the ECL intensity of AgCysNR. The linear range of the ECL immunosensor was 10 fg/mL to 100 ng/mL, and the detection limit was 2.3 fg/mL (signal/noise = 3). The sensor was determined to be stable, repeatable, and reproducible, and the method achieved recoveries of 101.0 to 102.6% with relative standard deviations of 1.4 to 2.0%. This immunosensor represents a promising tool for the early diagnosis of AMI.

Keywords: Biosensor; Electrochemiluminescence; Luminophore; Silver-cysteine nanorod.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Immobilized / immunology
  • Biosensing Techniques* / methods
  • Cysteine* / analysis
  • Cysteine* / chemistry
  • Electrochemical Techniques* / instrumentation
  • Electrochemical Techniques* / methods
  • Fatty Acid Binding Protein 3 / analysis
  • Fatty Acid Binding Protein 3 / blood
  • Fatty Acid-Binding Proteins / analysis
  • Fatty Acid-Binding Proteins / blood
  • Humans
  • Immunoassay / methods
  • Limit of Detection*
  • Luminescent Measurements* / methods
  • Metal Nanoparticles* / chemistry
  • Molybdenum / chemistry
  • Myocardial Infarction / diagnosis
  • Nanotubes* / chemistry
  • Oxides / chemistry
  • Silver* / chemistry

Substances

  • Cysteine
  • Silver
  • Molybdenum
  • Fatty Acid Binding Protein 3
  • Oxides
  • Antibodies, Immobilized
  • FABP3 protein, human
  • Fatty Acid-Binding Proteins