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首页> 外文期刊>Journal of Hazardous Materials >Selective binding of antibiotics using magnetic molecular imprint polymer (MMIP) networks prepared from vinyl-functionalized magnetic nanoparticles
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Selective binding of antibiotics using magnetic molecular imprint polymer (MMIP) networks prepared from vinyl-functionalized magnetic nanoparticles

机译:使用由乙烯基官能化磁性纳米粒子制备的磁性分子印记聚合物(MMIP)网络的抗生素选择性结合

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摘要

Adverse effects of pharmaceutical emerging contaminants (PECs), including antibiotics, in water supplies has been a global concern in recent years as they threaten fresh water security and lead to serious health problems to human, wildlife and the environment. However, detection of these contaminants in water sources, as well as food products, is difficult due to their low concentration. Here, we prepared a new family of magnetic molecular imprinted polymer (MMIP) networks for binding antibiotics via a microemulsion polymerization technique using vinyl silane modified Fe3O4 magnetic nanoparticles. The cross-linked polymer backbone successfully integrated with 20-30 nm magnetic nanoparticles and generated a novel porous polymeric network structure. These networks showed a high binding capacity for both templates, erythromycin and ciprofloxacin at 70 and 32 mg/g. Both MMIPs were also recyclable, retaining 75 % and 68 % of the binding capacity after 4 cycles. These MMIPs have showed a clear preference for binding the template molecules, with a binding capacity 4- to 7-fold higher than the other antibiotics in the same matrix. These results demonstrate our MMIP networks, which offered high binding capacity and selectivity as well as recyclability, can be used for both removal and monitoring hazardous antibiotic pollutants in different sources/samples and food products.
机译:药物新出现的污染物(PEC)(包括抗生素)在水供应中的不良反应近年来威胁着淡水安全性并导致人类,野生动物和环境的严重健康问题,这是全球性的关注。然而,由于其低浓度,难以检测水源中的这些污染物,以及食物。这里,我们制备了一种新的磁性分子印迹聚合物(MMIP)网络,用于使用乙烯基硅烷改性Fe3O4磁性纳米粒子通过微乳液聚合技术结合抗生素。交联聚合物骨架与20-30nm磁性纳米颗粒成功集成并产生了一种新型多孔聚合物网络结构。这些网络显示出在70和32mg / g的模板,红霉素和环丙沙星的高结合能力。两种MMIP也可回收,保留4个循环后的结合能力的75%和68%。这些MMIPS表明结合模板分子的清晰偏好,其结合能力低于同一基质中的其他抗生素的结合能力4-至7倍。这些结果证明了我们的MMIP网络,其提供高结合能力和选择性以及可再循环性,可用于除去和监测不同来源/样品和食品的危险抗生素污染物。

著录项

  • 来源
    《Journal of Hazardous Materials》 |2020年第5期|121709.1-121709.10|共10页
  • 作者单位

    Heriot Watt Univ Sch Engn & Phys Sci Chem Engn Edinburgh EH14 4AS Midlothian Scotland;

    Hacettepe Univ Inst Sci Nanotechnol & Nanomed Div Ankara Turkey;

    Yuksek Ihtisas Univ Med Lab Tech Vocat Sch Hlth Serv Ankara Turkey;

    Heriot Watt Univ Sch Engn & Phys Sci Chem Engn Edinburgh EH14 4AS Midlothian Scotland;

    Heriot Watt Univ Sch Engn & Phys Sci Chem Engn Edinburgh EH14 4AS Midlothian Scotland;

    Hacettepe Univ Inst Sci Nanotechnol & Nanomed Div Ankara Turkey;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Magnetic MIP; Erythromycin ERY; Ciprofloxacin CPX; 3-butenyltriethoxysilane; Poly(methacrylic acid) PMAA;

    机译:磁壁;红霉素胺;环丙沙星CPX;3-丁烯基三乙氧基硅烷;聚(甲基丙烯酸)PMAA;

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