4.7 Article

Molecularly imprinted ratiometric electrochemical sensor based on carbon nanotubes/cuprous oxide nanoparticles/titanium carbide MXene composite for diethylstilbestrol detection

期刊

MICROCHIMICA ACTA
卷 189, 期 4, 页码 -

出版社

SPRINGER WIEN
DOI: 10.1007/s00604-022-05249-x

关键词

Electrochemical sensors; Molecularly imprinted polymers; Ratiometric strategy; Diethylstilbestrol; Titanium carbide; Cuprous oxide

资金

  1. National Natural Science Foundation of China [21775112]

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In this study, a reliable detection of DES was achieved through a ratiometric strategy employing Cu2O nanoparticles as inner reference probe. The sensitivity of the sensor was further improved by introducing modified electrodes and CNT. The application of the sensor in real samples demonstrated its high sensitivity and accuracy for DES detection.
Conventional molecularly imprinted polymers (MIP)-based electrochemical sensors are generally susceptible to the changes of personal operation, electrode surface, and solution conditions. Herein, a ratiometric strategy was employed through introducing Cu2O nanoparticles (NPs) as inner reference probe to realize the reliable detection of diethylstilbestrol (DES). MIP film was prepared by electropolymerization of 1H-pyrrole-3-carboxylicacid in the presence of DES on carbon nanotubes/cuprous oxide/titanium carbide (CNT/Cu2O NPs/Ti3C2Tx) modified electrodes. The Ti3C2Tx with accordion-like structure not only possessed good electrical conductivity, but also facilitated the immobilization of Cu2O NPs, which contributed to stabilizing the signal. CNT was introduced to further improve the sensitivity of the sensor. Under optimum conditions, the MIP/CNT/Cu2O NPs/Ti3C2Tx electrochemical sensors showed a broad linear response range of 0.01 to 70 mu M, and a low detection limit of 6 nM (S/N = 3). Moreover, the sensor was applied to detect DES in real samples including lake water, milk, and pork, and the recoveries for spiked standard were 88-112%. Thus, this work provides a new way for reliable DES detection.

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