AI Article Synopsis

  • Diagnosis of visceral leishmaniasis is complicated due to similarities with other diseases like malaria and tuberculosis, necessitating effective detection methods.
  • A novel immunosensor was developed using a CoFeO-C60 nanocomposite and an A2 peptide antigen to identify specific antibodies, showcasing advanced techniques for characterization and testing.
  • The immunosensor demonstrated high reproducibility and sensitivity, with a detection range of 10-10 µg/mL and a limit of 30.34 fg/mL, indicating its promising utility for diagnosing visceral leishmaniasis.

Article Abstract

Diagnosis of Visceral Leishmaniasis is challenging due to the shared clinical features with malaria, typhoid, and tuberculosis. A CoFeO-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 (NH-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 CoFeO-C60-modified electrode. The performance of the immunosensor, Apg-CoFeO-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)] 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 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.

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Source
http://dx.doi.org/10.1016/j.bioelechem.2024.108662DOI Listing

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