| نویسندگان | Majid Kalatebojdi,elahe arabi ayask |
| نشریه | Analytical and Bioanalytical Electrochemistry |
| شماره صفحات | 568-582 |
| شماره سریال | 17 |
| شماره مجلد | 7 |
| نوع مقاله | Full Paper |
| تاریخ انتشار | 2025 |
| نوع نشریه | الکترونیکی |
| کشور محل چاپ | ایران |
| نمایه نشریه | isc،Scopus |
| کلید واژه ها | Agarose membrane; Deep eutectic solvent; Fluorescence detection; Gel, electromembrane extraction; Nilotinib |
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چکیده مقاله
A novel and eco-friendly approach is introduced for the quantification of nilotinib in biological samples, employing gel-based electromembrane extraction (G-EME) coupled with fluorescence detection. In this method, a deep eutectic solvent (DES) composed of choline chloride and methacrylic acid (ChCl–MAA) was incorporated into agarose membranes (AG@DESChCl–MAA) to enhance extraction performance. The inclusion of DES significantly improved the conductivity, selectivity, and migration efficiency of nilotinib across the membrane. This system offers several advantages, including simplicity of operation, low cost, portability, and the elimination of toxic organic solvents. The developed method demonstrated good precision, with intra- and inter-day relative standard deviations (RSDs) of 6.5% and 8.6%, respectively. A linear calibration curve was obtained in the concentration range of 0.65 to 10.0 mg·L⁻¹, with a detection limit (LOD) of 0.20 mg·L⁻¹. These results confirm theepotential of the AG@DESChCl–MAA-based G-EME system as a sensitive, green, and costeffective alternative for nilotinib analysis in complex matrices.
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