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Supersensitive Photoelectrochemical Aptasensor Based on Br,N-Codoped TiO2 Sensitized by Quantum Dots

机译:基于BR的超敏光电化学Aptasensor,由量子点致敏的N-划分的TiO2

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摘要

Here, we fabricated a novel photoelectrochemical (PEC) aptasensor based on Br,N-codoped TiO2/CdS quantum dots (QDs) sensitization structure with excellent energy level arrangement for supersensitive detection of carcinoembryonic antigen (CEA). The prepared Br,N-codoped TiO2 could reduce the energy bandwidth of TiO2 from 3.2 to 2.88 eV, which could dramatically reduce the basic signal and obviously broaden the absorption of light (400-700 nm). In addition, the energy bandwidth of Br,N-codoped TiO2 (2.88 eV) matched well with that of CdS QDs (2.4 eV), making CdS QDs an ideal signal enhancer for amplifying the photocurrent signal of Br,N-codoped TiO2. More importantly, the constructed Br,N-codoped TiO2/CdS QDs sensitization structure with narrow energy level gradient enabled the effective promotion of electron -transfer capability and dramatic improvement of photoelectric conversion efficiency. Simultaneously, a small amount of the CEA was transformed into substantial single-chain DNA (T-DNA) via exonuclease III (Exo-III)-assisted cycle strategy. Under optimum conditions, the designed PEC aptasensor demonstrated a wide detection range from 1 fg/mL to 1 ng/mL and a low detection limit as 0.46 fg/mL for CEA assay. This strategy prepared a new photoactive material to markedly improve photoelectric conversion efficiency and initiated a new way to realize the highly sensitive PEC biomolecules detection.
机译:在这里,我们基于BR,N型TiO2 / Cds量子点(QDS)敏化结构的新型光电化学(PEC)Aptasensor,其具有优异的能级布置,用于超敏检测癌丙烯抗原(CEA)。制备的BR,N编码TiO2可以将TiO2的能量带宽从3.2降低到2.88eV,这可能会显着降低基本信号,并且显然拓宽光的吸收(400-700nm)。另外,BR,N型TiO2(2.88eV)的能量带宽与CDS QD(2.4eV)的匹配良好,使CDS QD是用于放大BR,N型TiO2的光电流信号的理想信号增强剂。更重要的是,具有窄能级梯度的构建的BR,N编码的TiO2 / CDS QDS致敏结构使得能够有效促进电子 - 转换能力和光电转换效率的显着提高。同时,将少量CEA通过外切核酸酶III(EXO-III)级循环策略转化为基本单链DNA(T-DNA)。在最佳条件下,设计的PEC Aptasensor在1fg / ml至1ng / ml的宽检测范围和用于CEA测定的0.46fg / ml的低检测限度。该策略准备了一种新的光活性材料,可显着提高光电转换效率,并开始实现高敏感的PEC生物分子检测的新方法。

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  • 来源
    《Analytical chemistry》 |2019年第16期|共6页
  • 作者单位

    Southwest Univ Coll Chem &

    Chem Engn Minist Educ Key Lab Luminescent &

    Real Time Analyt Chem Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Minist Educ Key Lab Luminescent &

    Real Time Analyt Chem Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Minist Educ Key Lab Luminescent &

    Real Time Analyt Chem Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Minist Educ Key Lab Luminescent &

    Real Time Analyt Chem Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Minist Educ Key Lab Luminescent &

    Real Time Analyt Chem Chongqing 400715 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
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