4.7 Article

Fast microwave-assisted synthesis of magnetic molecularly imprinted polymer for sulfamethoxazole

期刊

TALANTA
卷 232, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.talanta.2021.122430

关键词

Molecularly imprinted polymer; Microwave synthesis; Magnetic nanoparticles; Computational approach; Sulfamethoxazole

资金

  1. Erasmus+ KA107 (EU) Program of the University of Cadiz (Spain), through `Servicio Espanol para la Internacionalizacion de la Educacion' (SEPIE)
  2. Institute of Research on Electron Microscopy and Materials (IMEYMAT, project APPLIED-SENS)
  3. Programa de fomento e impulso de la investigacion y de la transferencia de la Universidad de Cadiz 2020-2021 [PR2020-013]
  4. Junta de Andalucia (PAIDI2020)

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A fast and simple strategy based on the microwave technique for the preparation of magnetic molecularly imprinted polymers (MMIPs) is proposed for the selective determination of sulfamethoxazole (SMX). The study involved computational design, synthesis, characterization, and application of MMIPs using different monomers, with experimental results confirming the computational approach. Both MMIPs showed good selectivity and sensitivity for SMX detection, with MMIP-MAA demonstrating higher recovery values in real sample (tap water) analysis compared to MMIP-AM.
A fast and simple strategy based on the microwave technique for the preparation of magnetic molecularly imprinted polymers (MMIPs) is proposed for the selective determination of sulfamethoxazole (SMX). The MMIPs were synthesized at 70 degrees C in 20 min, being much faster than the conventional techniques. A computational approach based on density functional theory was used to design the MMIP and compare the two most used monomers in MIPs, including methacrylic acid (MAA) and acrylamide (AM). Then, two different MMIPs were prepared using AM and MAA as monomers. The resultant materials were characterized with X-ray diffraction, thermogravimetric analysis, scanning/transmission electron microscopy, and Fourier-transform infrared spectroscopy. Besides, the adsorption characterizations suggested that the adsorption of SMX followed the pseudosecond-order model in the kinetic study and the Sips model in the isotherm study. The experimental results corroborated the computational approach. Furthermore, Both MMIPs demonstrated good selectivity. The MMI-PAM and MMIP-MAA were applied as adsorbents in magnetic dispersive solid-phase extraction combined with UV-visible spectroscopy to quantify SMX. The obtained limits of detection and quantification were lower than 0.59 and 1.77 mu M, respectively for both MMIPs. The sensitivity of both MMIPs was in the range of 0.021-0.023 (SI). Our findings revealed that there is no significant difference in the analytical parameters between MMIP-AM and MMIP-MAA. However, the application of both MMIPs in a real sample (tap water) showed that the recovery values of SMX obtained with MMIP-AM (68-70%) were lower than that with MMIP-MAA (80-90%) suggesting that MMIP-MAA is more appropriate for SMX determination.

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