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首页> 外文期刊>Analytical Letters >Electrochemical Determination of Aflatoxin B1 (AFB1) Using a Copper-Based Metal-Organic Framework (Cu-MOF) and Gold Nanoparticles (AuNPs) with Exonuclease III (Exo III) Assisted Recycling by Differential Pulse Voltammetry (DPV)
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Electrochemical Determination of Aflatoxin B1 (AFB1) Using a Copper-Based Metal-Organic Framework (Cu-MOF) and Gold Nanoparticles (AuNPs) with Exonuclease III (Exo III) Assisted Recycling by Differential Pulse Voltammetry (DPV)

机译:使用铜基金属 - 有机骨架(Cu-Mof)和金纳米颗粒(AUNP)与外切核酸酶III(EXO III)的电化学测定磷酸盐毒素B1(AFB1)辅助脉冲伏安法(DPV)辅助回收

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摘要

A sensitive electrochemical biosensor was designed for determination of aflatoxin B1 (AFB1) using a copper-based metal-organic framework (Cu-MOF), which has strong electrochemical activity and exonuclease III (Exo III)-assisted recycling for dual signal amplification. Hairpin DNA (S1) was immobilized on the electrode. The AFB1 was recognized by aptamer DNA (S2) and complementary DNA (S3) was released. The S3 hybridized with the hairpin S1 to form the Exo III hydrolyzed double-stranded DNA, leaving a partial sequence of hairpin DNA (S1 ') on the electrode and releasing S3 for the next cycle of the opening and digestion of hairpin S1. The amplified S1 ' then was able to combine with more signal probes. Cu-MOF bond gold nanoparticles (AuNPs) by -NH2 were immobilized to capture DNA (S4) to obtain Cu-MOF/AuNPs/S4. This signal probe Cu-MOF/AuNPs/S4 was able to hybridize with the electrode and generate an amplified electrochemical signal. Under the optimized conditions, this electrochemical biosensor for AFB1 exhibited a low detection limit of 6.7 x 10(-7) ng/mL at a signal-to-noise equal to 3 and a wide linear range from 10(-6) to 1 ng/mL. The biosensor was also used to analyze AFB1-spiked beer sample with recovery values between 96% and 103%. This method has the potential to become a valuable technology for detecting various toxins by the selection of the appropriate aptamer DNA.
机译:使用铜基金属 - 有机骨架(Cu-MOF)来确定敏感的电化学生物传感器,用于测定黄曲霉毒素B1(AFB1),其具有强大的电化学活性和外切核酸酶III(EXO III) - 用于双信号放大的回收。将发夹DNA(S1)固定在电极上。通过适体DNA(S2)识别AFB1并释放互补DNA(S3)。用发夹S1杂交的S3以形成EXO III水解的双链DNA,留下电极上的发夹DNA(S1')的部分序列并释放S3,用于发夹S1的开口和消化的下一个循环。然后,放大的S1'能够与更多的信号探针组合。将Cu-MOF键合金纳米颗粒(AUNP)固定为捕获DNA(S4)以获得Cu-Mof / AuNPS / S4。该信号探针Cu-MOF / AUNPS / S4能够与电极杂交并产生放大的电化学信号。在优化条件下,对于AFB1的这种电化学生物传感器在等于3的信号到噪声下显示出6.7×10(-7)Ng / mL的低检测限,并且从10(-6)至1 ng的宽线性范围/ ml。生物传感器还用于分析AFB1 - 尖峰啤酒样品,回收率为96%和103%。该方法具有通过选择适当的适体DNA来检测各种毒素的有价值的技术。

著录项

  • 来源
    《Analytical Letters》 |2019年第18期|共15页
  • 作者单位

    Nanjing Normal Univ Jiangsu Key Lab New Power Batteries Jiangsu Collaborat Innovat Ctr Biomed Funct Mat Jiangsu Key Lab Biomed Mat Coll Chem &

    Mat Sci 1 Wenyuan Rd Nanjing 210023 Jiangsu Peoples R China;

    Nanjing Normal Univ Jiangsu Key Lab New Power Batteries Jiangsu Collaborat Innovat Ctr Biomed Funct Mat Jiangsu Key Lab Biomed Mat Coll Chem &

    Mat Sci 1 Wenyuan Rd Nanjing 210023 Jiangsu Peoples R China;

    Nanjing Normal Univ Jiangsu Key Lab New Power Batteries Jiangsu Collaborat Innovat Ctr Biomed Funct Mat Jiangsu Key Lab Biomed Mat Coll Chem &

    Mat Sci 1 Wenyuan Rd Nanjing 210023 Jiangsu Peoples R China;

    Nanjing Normal Univ Jiangsu Key Lab New Power Batteries Jiangsu Collaborat Innovat Ctr Biomed Funct Mat Jiangsu Key Lab Biomed Mat Coll Chem &

    Mat Sci 1 Wenyuan Rd Nanjing 210023 Jiangsu 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

    Aflatoxin B1 (AFB1); copper-based metal-organic framework (Cu-MOF); differential pulse voltammetry (DPV); dual signal amplification; exonuclease III (Exo III);

    机译:黄曲霉毒素B1(AFB1);铜基金属 - 有机框架(CU-MOF);差分脉冲伏安法(DPV);双信号放大;Exonuclease III(EXO III);

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