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Updated: Jan 11, 2026

ELIME Enzyme Linked Immuno Magnetic Electrochemical Method for Mycotoxin Detection
Published on: October 23, 2009
Engineering high-affinity and selective molecular recognition redox active imprinted platform on carbon cloth for
Aqsa Tariq1, Seham J F Alanazi2, Mian Hasnain Nawaz1
1Interdisciplinary Research Centre in Biomedical Materials (IRCBM), COMSATS University, Islamabad, Lahore Campus, Lahore 54000, Pakistan.
Abstract:
A novel dual-functional redox-controllable molecularly imprinted polymer (MIP)-based electrochemical sensor for the sensitive detection and efficient microextraction of aflatoxin B1 (AFB1) was developed in this study, filling an essential void in food safety monitoring. The β-CFe@MIP/CC sensor was engineered by UV-curing beta-cyclodextrin-ferrocene (β-CFe) conjugates and conventional monomers onto a carbon cloth matrix. The synergistic role of β-cyclodextrin (βCD) to increase host-guest interaction ensures high selectivity towards AFB1, and ferrocene (Fe) enhances redox cycling efficiency, enhancing the electrochemical signal. Specifically, the binding of AFB1 with β-CFe@MIP/CC through recognition pockets that controlled the electron transfer and exhibited an imprinting factor (IF) ∼ 6 thus accurately detecting the toxins. The sensor showed an excellent linear detection range of 0.3-1500 ng/mL, LOD of 0.03 ng/mL and LOQ of 0.1 ng/mL. The sensor exhibited excellent reproducibility across real milk, wheat and corn samples with a recovery rates between 98.6 and 104.7 % with low RSD values (0.35-2.83 %) and displayed remarkable selectivity, differentiating AFB1 from structurally related mycotoxins. This bimodal sensor exhibited extraordinary microextraction efficiency for AFB1 in milk samples, extensively reducing the contamination levels across all tested concentrations. The obtained results were validated with standard High-performance liquid chromatography (HPLC) analysis of the milk samples pre and post-incubation with β-CFe@MIP/CC. The sensor's high adsorption capacity, binding specificity and detoxification efficacy establish it as a superior tool for integration into routine milk quality monitoring systems.

