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Rapid and selective detection of Fe (III) by using a smartphone-based device as a portable detector and hydroxyl functionalized metal-organic frameworks as the fluorescence probe

机译:通过使用基于智能手机的装置作为便携式检测器和羟官能化金属 - 有机框架的快速和选择性地检测Fe(III)作为荧光探针

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摘要

Here, a label-free fluorescent sensor was developed for detection Fe (III) by utilizing the quenching effect of Fe (III) on the fluorescence of the hydroxyl functionalized metal-organic framework MIL-53(Fe)-(OH)(2), which was synthesized by using a one-step solvothermal method. The specific binding interaction between Fe (III) and hydroxyl facilitated the absorption of free Fe (III) to MIL-53(Fe)-(OH)(2), which leads to rapid fluorescent intensity quenching effect. The potential quenching mechanism was proved to be the photo-induced electron transfer (PET) from electron-rich ligands of MIL-53(Fe)-(OH)(2) to the half-filled 3d orbitals of free Fe (III) in the sample solution. For in-field applications, the fluorescence signal was detected rapidly by using a homemade 3D-printed, portable, and low-cost smartphone sensor. A commercial 365 nm UV LED light was adopted as the excitation light source, while the camera in a smartphone was utilized as the optical detector. The fluorescent signals obtained by using the smartphone sensor were in a good agreement with those obtained from a commercial microplate reader. Under the optimal assay conditions, the linear detection range of Fe (III) was 5.0-200 mu M, and the limit of detection is 1.7 mu M. This result is compatible with the commercial microplate reader. The developed method was successfully adopted to detect Fe (III) in human serum and environmental water samples with acceptable recovery values of 90-108.5%. The portable, low-cost, fast-response, user-friendly and sensitive fluorescent protocol based on a self-quenching fluorescent nanoprobe can be conducted at home or anywhere else without sophisticated instruments, showing a great application potential in clinical diagnosis, on-site environmental monitoring and healthcare at home. (C) 2019 Elsevier B.V. All rights reserved.
机译:这里,通过利用Fe(III)对羟基官能化金属 - 有机框架MIL-53(Fe) - (OH)(2)的荧光对荧光淬火效果来开发无标签荧光传感器,通过使用一步的溶液方法合成。 Fe(III)和羟基之间的特异性结合相互作用促进了游离Fe(III)至MIL-53(Fe) - (OH)(2)的吸收,这导致快速荧光强度猝灭效果。被证明是潜在的淬火机制是来自MIL-53(Fe) - (2)的富含电子富含电子的配体的光诱导的电子转移(PET),以至于FRE FE(III)的半填充的3D轨道样品溶液。对于现场应用,通过使用自制3D印刷,便携式和低成本智能手机传感器快速检测荧光信号。采用商业365nm UV LED光作为激励光源,而智能手机中的相机用作光学检测器。通过使用智能手机传感器获得的荧光信号与从商业微孔板读卡器获得的那些良好。在最佳测定条件下,Fe(III)的线性检测范围为5.0-200μm,检测极限为1.7μm。该结果与商业微孔板读卡器兼容。成功采用开发的方法来检测人血清和环境水样中的Fe(III),恢复值为90-108.5%。基于自猝灭荧光纳米骨瓣的便携式,低成本,快速响应,用户友好敏感的荧光协同,可以在家中或任何其他任何地方进行,没有复杂的仪器,在现场临床诊断中显示出很大的应用潜力在家环境监测和医疗保健。 (c)2019年Elsevier B.V.保留所有权利。

著录项

  • 来源
    《Analytica chimica acta》 |2019年第2019期|共7页
  • 作者单位

    Shenzhen Univ Coll Mat Sci &

    Engn Shenzhen Key Lab Polymer Sci &

    Technol Shenzhen 518060 Peoples R China;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Shenzhen Univ Coll Mat Sci &

    Engn Shenzhen Key Lab Polymer Sci &

    Technol Shenzhen 518060 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

    Metal-organic frameworks; Fluorescence; Portable smartphone sensor; Fe(III);

    机译:金属 - 有机框架;荧光;便携式智能手机传感器;FE(III);
  • 入库时间 2022-08-20 16:40:24

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