首页> 外文OA文献 >Preparation of Fluorescent Molecularly Imprinted Polymers via Pickering Emulsion Interfaces and the Application for Visual Sensing Analysis of Listeria Monocytogenes
【2h】

Preparation of Fluorescent Molecularly Imprinted Polymers via Pickering Emulsion Interfaces and the Application for Visual Sensing Analysis of Listeria Monocytogenes

机译:通过皮克林乳液界面制备荧光分子印迹聚合物及李斯特菌单核细胞增生的视觉感测分析

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

In this work, a novel molecularly imprinted polymer (MIP) with water-soluble CdTe quantum dots (QDs) was synthesized by oil-in-water Pickering emulsion polymerization using whole Listeria monocytogenes as the template. Listeria monocytogenes was first treated by acryloyl-functionalized chitosan with QDs to form a bacteria−chitosan network as the water phase. This was then stabilized in an oil-in-water emulsion comprising a cross-linker, monomer, and initiator, causing recognition sites on the surface of microspheres embedded with CdTe QDs. The resulting MIP microspheres enabled selective capture of the target bacteria via recognition cavities. The target bacteria Listeria monocytogenes was detected. Scanning electron microscopy (SEM) characterization showed that the MIPs had a rough spherical shape. There was visual fluorescence detection via quenching in the presence of the target molecule, which offered qualitative detection of Listeria monocytogenes in milk and pork samples. The developed method simplified the analysis process and did not require any sample pretreatment. In addition, the fluorescence sensor provided an effective, fast, and convenient method for Listeria monocytogenes detection in food samples.
机译:在这项工作中,通过使用全部李斯特菌单核细胞增生作为模板,通过水包油的乳液聚合来合成具有水溶性CdTe量子点(QDS)的新型分子印迹聚合物(MIP)。首先通过丙烯酰基官能化的壳聚糖用QDS处理李斯特菌单核细胞增生,以形成细菌 - 壳聚糖网络作为水相。然后将其稳定在水包油乳液中,其包含交联剂,单体和引发剂,导致嵌入CdTe QDS的微球表面上的识别位点。得到的MIP微球通过识别腔使靶细菌的选择性捕获能够。检测到靶细菌李斯特菌单核细胞增生。扫描电子显微镜(SEM)表征显示,MIPS具有粗糙的球形。在靶分子存在下通过猝灭存在视觉荧光检测,其在牛奶和猪肉样品中提供了李斯特菌单核细胞增生的定性检测。开发方法简化了分析过程,不需要任何样品预处理。此外,荧光传感器提供了一种有效,快速,方便的食品样品中李斯特菌单核细胞增生的方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号