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ß-Cyclodextrin-/AuNPs-functionalized covalent organic framework-based magnetic sorbent for solid phase extraction and determination of sulfonamides.
Yang, Yan; Li, Guoliang; Wu, Di; Wen, Aying; Wu, Yongning; Zhou, Xuxia.
Afiliación
  • Yang Y; School of Food and Biological Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, China.
  • Li G; School of Food and Biological Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, China. 61254368@163.com.
  • Wu D; Key Laboratory of Life-Organic Analysis of Shandong Province, Qufu Normal 13 University, Qufu, 273165, China. 61254368@163.com.
  • Wen A; Yangtze Delta Region Institute of Tsinghua University, Zhejiang, 314006, China.
  • Wu Y; School of Food and Biological Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, China.
  • Zhou X; NHC Key Laboratory of Food Safety Risk Assessment; Food Safety Research Unit (2019RU014) of Chinese Academy of Medical Science; China National Center for 11 Food Safety Risk Assessment, Beijing, 100050, China.
Mikrochim Acta ; 187(5): 278, 2020 04 20.
Article en En | MEDLINE | ID: mdl-32314062
ABSTRACT
ß-Cyclodextrin-functionalized magnetic covalent organic framework (Fe3O4@COF@Au-ß-CD) was developed as sorbent for magnetic solid phase extraction of trace sulfonamides in meat samples prior to HPLC-MS/MS analysis. The sorbent was synthesized by loading gold nanoparticles onto a Fe3O4@COF surface and then functionalized by thiolated-ß-cyclodextrin immobilization via Au-S bonding formation. The prepared composite material was employed for sulfonamides extraction. The main parameters were optimized to obtain the best extraction efficiency. The experiments of adsorption kinetics were carried out to investigate the adsorption mechanism. Results showed the pseudo-second-order kinetic was better fitted with the adsorption kinetics of sulfonamides. Under optimized conditions, the magnetic solid phase extraction-HPLC method showed good linearity (R2 ≥ 0.9936), and the limits of detection were in the range of 0.8-1.6 µg kg-1. The proposed method was successfully used for quantitation of sulfonamides in real samples. The recoveries ranged from 78.9 to 112.0% with relative standard deviations (RSDs) < 10% (n = 5). The proposed method exhibited great potential for enrichment and determination of sulfonamides in many other food or environment samples. Graphical abstract.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Mikrochim Acta Año: 2020 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Mikrochim Acta Año: 2020 Tipo del documento: Article País de afiliación: China