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Fabrication of amino- and hydroxyl dual-functionalized magnetic microporous organic network for extraction of zearalenone from traditional Chinese medicine prior to the HPLC determination.

Authors
  • Li, Xue1
  • Wang, Meng-Yao1
  • Wang, Yu1
  • Yang, Wen-Zhi2
  • Yang, Cheng-Xiong3
  • 1 Haihe Laboratory of Modern Chinese Medicine, 10 Poyanghu Road, Tianjin 301617, China; National Key Laboratory of Chinese Medicine Modernization, State Key Laboratory of Component-Based Chinese Medicine, Tianjin University of Traditional Chinese Medicine, 10 Poyanghu Road, Tianjin 301617, China. , (China)
  • 2 Haihe Laboratory of Modern Chinese Medicine, 10 Poyanghu Road, Tianjin 301617, China; National Key Laboratory of Chinese Medicine Modernization, State Key Laboratory of Component-Based Chinese Medicine, Tianjin University of Traditional Chinese Medicine, 10 Poyanghu Road, Tianjin 301617, China. Electronic address: [email protected]. , (China)
  • 3 School of Pharmaceutical Sciences & Institute of Materia Medica, Medical Science and Technology Innovation Center, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, Shandong 250117, China. Electronic address: [email protected]. , (China)
Type
Published Article
Journal
Journal of chromatography. A
Publication Date
Apr 18, 2024
Volume
1724
Pages
464915–464915
Identifiers
DOI: 10.1016/j.chroma.2024.464915
PMID: 38663319
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

Efficient enrichment of trace zearalenone (ZEN) from the complex traditional Chinese medicine (TCM) samples is quite difficult, but of great significance for TCM quality control. Herein, we reported a novel magnetic solid phase extraction (MSPE) strategy for ZEN enrichment using the amino- and hydroxyl dual-functionalized magnetic microporous organic network (Fe3O4@MON-NH2-OH) as an advanced adsorbent combined with the high-performance liquid chromatography (HPLC) determination. Efficient extraction of ZEN was achieved via the possible hydrogen bonding, hydrophobic, and π-π interactions between Fe3O4@MON-NH2-OH and ZEN. The adsorption capacity of Fe3O4@MON-NH2-OH for ZEN was 215.0 mg g-1 at the room temperature, which was much higher than most of the reported adsorbents. Under the optimal condition, the developed Fe3O4@MON-NH2-OH-MSPE-HPLC method exhibited wide linear range (5-2500 μg L-1), low limits of detection (1.4-35 μg L-1), less adsorbent consumption (5 mg), and large enhancement factor (95) for ZEN. The proposed method was successfully applied to detect trace ZEN from 10 kinds of real TCM samples. Conclusively, this work demonstrates the Fe3O4@MON-NH2-OH can effectively extract trace ZEN from the complex TCM matrices, which may open up a new way for the application of MONs in the enrichment and extraction of trace contaminants or active constituents from the complex TCM samples. Copyright © 2024 Elsevier B.V. All rights reserved.

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