Built-in thiol mesoporous carbon immunosensor to detect carcinoembryonic antigen in human serum

A label-free electrochemical immunosensor for carcinoembryonic antigens (CEA) detection is reported based on a built-in thiol-mesoporous carbon architecture. The material was functionalized with 3-maleimidepropionic acid to immobilize anti-CEA antibodies. The immunosensor was characterized using field-emission scanning electron microscopy, X-ray photoelectron spectroscopy, cyclic voltammetry, and electrochemical impedance spectroscopy. Biorecognition events were monitored by differential pulse voltammetry, with current intensity dependent on protein concentration. The device exhibited a linear range of 1–10 ng mL-1 for CEA, with a clinically relevant limit of detection of 1.02 ng mL-1. The immunosensor successfully detected CEA in human serum samples, with results comparable to those obtained by a standard spectrophotometric method. This platform has proven to be a promising alternative for the prognosis and management of patients with colorectal cancer, as well as having significant potential for point-of-care diagnosis.

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Publication Details

Journal
Microchimica Acta
Published
2026-04-13
DOI
https://doi.org/10.1007/s00604-026-07987-8
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Built-in thiol mesoporous carbon immunosensor to detect carcinoembryonic antigen in human serum

Danilo Echeverri, Jahir Orozco, Néstor Llinás-Quintero, Jennifer Laverde et al.
Microchimica Acta
Advanced biosensing and bioanalysis techniques
article

Built-in thiol mesoporous carbon immunosensor to detect carcinoembryonic antigen in human serum

Danilo Echeverri, Jahir Orozco, Néstor Llinás-Quintero, Jennifer Laverde, Diana López, Luis Gerónimo Restrepo
article en

Abstract

A label-free electrochemical immunosensor for carcinoembryonic antigens (CEA) detection is reported based on a built-in thiol-mesoporous carbon architecture. The material was functionalized with 3-maleimidepropionic acid to immobilize anti-CEA antibodies. The immunosensor was characterized using field-emission scanning electron microscopy, X-ray photoelectron spectroscopy, cyclic voltammetry, and electrochemical impedance spectroscopy. Biorecognition events were monitored by differential pulse voltammetry, with current intensity dependent on protein concentration. The device exhibited a linear range of 1–10 ng mL-1 for CEA, with a clinically relevant limit of detection of 1.02 ng mL-1. The immunosensor successfully detected CEA in human serum samples, with results comparable to those obtained by a standard spectrophotometric method. This platform has proven to be a promising alternative for the prognosis and management of patients with colorectal cancer, as well as having significant potential for point-of-care diagnosis.

Microchimica ActaVol. 193(5)
Universidad de Antioquia (CO), Foundation for Clinical and Applied Cancer Research (CO), Instituto Tecnológico Metropolitano (CO)
Max-Planck-Gesellschaft, Universidad de Antioquia
Openalex Percentile: Top 24%
Advanced biosensing and bioanalysis techniques
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