A dual-electrode label-free immunosensor based on in situ prepared Au-MoO-Chi/porous graphene nanoparticles for point-of-care detection of cholangiocarcinoma.

Talanta

Center of Excellence for Trace Analysis and Biosensor, Prince of Songkla University, Hat Yai, Songkhla, 90110, Thailand; Center of Excellence for Innovation in Chemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, 90110, Thailand; Division of Health and Applied Sciences, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, 90110, Thailand; Forensic Science Innovation and Service Center, Prince of Songkla University, Hat Yai, Songkhla, 90110, Thailand. Electronic address:

Published: May 2024

AI Article Synopsis

  • A label-free electrochemical immunosensor was developed to detect CA19-9 and CEA, important biomarkers for cholangiocarcinoma, using a novel nanocomposite of gold nanoparticles, molybdenum trioxide, and chitosan.
  • The sensor's construction involved a layer-by-layer self-assembling technique on a dual screen-printed electrode, which enhanced its surface area and conductivity, improving antibody immobilization and sensitivity.
  • The immunosensor demonstrated reliable detection capabilities with specific concentration ranges and low limits of detection for both biomarkers, successfully analyzing human serum samples and achieving results comparable to standard clinical methods.

Article Abstract

A novel label-free electrochemical immunosensor was prepared for the detection of carbohydrate antigen 19-9 (CA19-9) and carcinoembryonic antigen (CEA) as biomarkers of cholangiocarcinoma (CCA). A nanocomposite of gold nanoparticles, molybdenum trioxide, and chitosan (Au-MoO-Chi) was layer-by-layer assembled on the porous graphene (PG) modified a dual screen-printed electrode using a self-assembling technique, which increased surface area and conductivity and enhanced the adsorption of immobilized antibodies. The stepwise self-assembling procedure of the modified electrode was further characterized morphologically and functionally. The electroanalytical detection of biomarkers was based on the interaction between the antibody and antigen of each marker via linear sweep voltammetry using ferrocyanide/ferricyanide as an electrochemical redox indicator. Under optimized conditions, the fabricated immunosensor showed linear relationships between current change (ΔI) and antigen concentrations in two ranges: 0.0025-0.1 U mL and 0.1-1.0 U mL for CA19-9, and 0.001-0.01 ng mL and 0.01-1.0 ng mL for CEA. The limits of detection (LOD) were 1.0 mU mL for CA19-9 and 0.5 pg mL for CEA. Limits of quantitation (LOQ) were 3.3 mU mL for CA19-9 and 1.6 pg mL for CEA. The selectivity of the developed immunosensor was tested on mixtures of antigens and was then successfully applied to determine CA19-9 and CEA in human serum samples, producing satisfactory results consistent with the clinical method.

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http://dx.doi.org/10.1016/j.talanta.2024.125755DOI Listing

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