Rapid and label-free A2 peptide epitope decorated CoFe2O4-C60 nanocomposite-based electrochemical immunosensor for detecting Visceral Leishmaniasis

Bioelectrochemistry. 2024 Jun:157:108662. doi: 10.1016/j.bioelechem.2024.108662. Epub 2024 Feb 7.

Abstract

Diagnosis of Visceral Leishmaniasis is challenging due to the shared clinical features with malaria, typhoid, and tuberculosis. A CoFe2O4-C60 nanocomposite-based immunosensor decorated with a sensitive A2 peptide antigen was fabricated to detect anti-A2 antibodies for application in visceral leishmaniasis diagnosis. The flame-synthesised nanocomposite was characterised using Fourier Transform Infrared spectroscopy (FTIR), X-ray diffraction spectroscopy (XRD), Scanning electron microscopy (SEM), Energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy and electrochemical impedance spectroscopy (EIS) techniques. N terminated specific A2 peptide epitope antigen (NH2-QSVGPLSVGP-OH) was synthesised and characterised by high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectroscopy (LC-MS). Using EDC/NHS, A2 peptide antigen (Apg) was immobilised on the CoFe2O4-C60-modified electrode. The performance of the immunosensor, Apg-CoFe2O4-C60NP/GCE, was evaluated by testing its ability to detect varying concentrations of anti-A2 antibody solution in PBS and spiked serum with 1 mM [Fe(CN)6]3-/4- in 0.01 M PBS (pH 7.4) as supporting electrolyte. using differential pulse voltammetry. The immunosensor showed excellent reproducibility and a linear range of 10-10-10-1 µg/mL, with an experimental detection limit of 30.34 fg/mL. These results suggest that the fabricated sensor has great potential as a tool for diagnosing visceral leishmaniasis.

Keywords: Anti-A2 antibodies; Cobalt-iron oxide–carbon nanocomposites; Immunosensor; Peptide antigen; Visceral Leishmaniasis.

MeSH terms

  • Antibodies
  • Biosensing Techniques* / methods
  • Electrochemical Techniques / methods
  • Epitopes
  • Humans
  • Immunoassay / methods
  • Leishmaniasis, Visceral* / diagnosis
  • Limit of Detection
  • Metal Nanoparticles* / chemistry
  • Nanocomposites* / chemistry
  • Peptides
  • Reproducibility of Results

Substances

  • Epitopes
  • Peptides
  • Antibodies