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Electroanalytical method development for the receptor tyrosine kinase inhibitor lenvatinib using a Ti3C2Tx-MXene based molecularly imprinted polymer modified carbon electrode.

Created on 02 Jul 2026

Authors

Mehmet Gülcan, Pınar Talay Pınar

Published in

Analytical and bioanalytical chemistry. Jul 01, 2026. Epub Jul 01, 2026.

Abstract

In this study, a Ti3C2Tx-MXene-based molecularly imprinted polymer sensor (MX/GCE-MiP) was developed for the electrochemical determination of the tyrosine kinase inhibitor lenvatinib. By combining the high surface area and conductivity of Ti3C2Tx-MXene with the selective recognition properties of molecularly imprinted polymers, a sensitive electrochemical sensing platform was obtained. The analytical performance of the sensor was evaluated by square-wave voltammetry (SWV) using the [Fe(CN)6]-3/-4 redox probe system after rebinding of lenvatinib within the imprinted cavities. Under optimized experimental conditions, the proposed sensor exhibited a linear response in the concentration range of 5.0-30.0 nM with a limit of detection (LOD) of 0.29 nM. Selectivity studies performed in the presence of dopamine, uric acid, ascorbic acid, and futibatinib demonstrated a significantly higher response toward lenvatinib under identical experimental conditions. In addition, the sensor showed good repeatability (3.20%), reproducibility (3.65%), and storage stability (4.1%). The applicability of the proposed sensor was preliminarily evaluated in synthetic serum and urine samples, yielding acceptable recovery values. Overall, the developed MX/GCE-MIP sensor provides a simple, sensitive, and cost-effective platform for the electrochemical detection of lenvatinib.

PMID:
42387095
Bibliographic data and abstract were imported from PubMed on 02 Jul 2026.

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