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首页> 外文期刊>Analytica chimica acta >Fluorescent aptasensor for antibiotic detection using magnetic bead composites coated with gold nanoparticles and a nicking enzyme
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Fluorescent aptasensor for antibiotic detection using magnetic bead composites coated with gold nanoparticles and a nicking enzyme

机译:用于抗生素检测的荧光AptaSensor使用磁珠复合材料涂覆有金纳米颗粒和切口酶的抗生素检测

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摘要

Antibiotic abuse has been bringing serious pollution in water, which is closely related to human health. It is desirable to develop a new strategy for antibiotic detection. To address this problem, a sensitive fluorescent aptasensor for antibiotic detection was developed by utilizing gold nanoparticles modified magnetic bead composites (AuNPs/MBs) and nicking enzyme. AuNPs/MBs were synthesized with the help of polyethylenimine (PEI). The prepared AuNPs/MBs acted as dual-functional scaffolds that owned excellent magnetic separation capacity and strong covalent bio-conjugation. The non-specifically absorbed aptamers in AuNPs/MBs were less than that in MBs. Hence, the fluorescent aptasensor based on AuNPs/MBs show a better signal to background ratio than that based on carboxyl modified magnetic beads (MBs). In this work, ampicillin was employed as a model analyte. In the presence of ampicillin, the specific binding between ampicillin and aptamer induced structure-switching that led to the release of partial complementary DNA (cDNA) of aptamer. Then, the released cDNA initiated the cycle of nicking enzyme assisted signal amplification (NEASA). Therefore, a large amount of taqman probes were cleaved and fluorescence signal was amplified. The prepared fluorescent aptasensor bring sensitive detection in range of 0.1-100 ng mL(-1) with the limit of detection of 0.07 ng mL(-1). Furthermore, this aptasensor was also successfully applied in real sample detection with acceptable accuracy. The fluorescent aptasensor provides a promising method for efficient, rapid and sensitive antibiotic detection. (C) 2017 Elsevier B.V. All rights reserved.
机译:抗生素滥用一直在水中造成严重污染,这与人类健康密切相关。希望开发一种新的抗生素检测策略。为了解决这个问题,通过利用金纳米颗粒改性的磁珠复合材料(AUNPS / MB)和切口酶,开发了一种用于抗生素检测的敏感荧光APTASESOR。在聚乙胺(PEI)的帮助下合成AUNPS / MBS。制备的AUNPS / MBS作用为双功能支架,具有优异的磁性分离能力和强烈的共价生物缀合。 AUNPS / MB中的非特异性吸收的适体小于MBS中的非特异性吸收的适体。因此,基于AUNPS / MBS的荧光APTASESEROR显示比基于羧基改性磁珠(MBS)的背景比的更好信号。在这项工作中,氨苄青霉素用作模型分析物。在氨苄青霉素存在下,氨苄青霉素和适体诱导的结构切换之间的特异性结合导致适体的部分互补DNA(cDNA)的释放。然后,释放的cDNA引发了切口酶辅助信号扩增(NEASA)的循环。因此,裂解大量的Taqman探针,并扩增荧光信号。制备的荧光Aptasensor在0.1-100ng ml(-1)范围内的敏感性检测,其检测限为0.07 ng ml(-1)。此外,这种APTASENSOR也以可接受的精度成功地应用于实际样品检测。荧光Aptasensor提供了有希望的有效,快速敏感的抗生素检测方法。 (c)2017 Elsevier B.v.保留所有权利。

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  • 来源
    《Analytica chimica acta》 |2017年第2017期|共8页
  • 作者单位

    Sichuan Univ Coll Life Sci Res Ctr Analyt Instrumentat Key Lab Bioresource &

    Ecoenvironm Minist Educ Chengdu 610064 Sichuan Peoples R China;

    Sichuan Univ Coll Life Sci Res Ctr Analyt Instrumentat Key Lab Bioresource &

    Ecoenvironm Minist Educ Chengdu 610064 Sichuan Peoples R China;

    Sichuan Univ Coll Life Sci Res Ctr Analyt Instrumentat Key Lab Bioresource &

    Ecoenvironm Minist Educ Chengdu 610064 Sichuan Peoples R China;

    Sichuan Univ Coll Life Sci Res Ctr Analyt Instrumentat Key Lab Bioresource &

    Ecoenvironm Minist Educ Chengdu 610064 Sichuan Peoples R China;

    Sichuan Univ Coll Life Sci Res Ctr Analyt Instrumentat Key Lab Bioresource &

    Ecoenvironm Minist Educ Chengdu 610064 Sichuan Peoples R China;

    Sichuan Univ Coll Life Sci Res Ctr Analyt Instrumentat Key Lab Bioresource &

    Ecoenvironm Minist Educ Chengdu 610064 Sichuan Peoples R China;

    Sichuan Univ West China Sch Publ Hlth Dept Lab Sci Publ Hlth Chengdu 610041 Sichuan Peoples R China;

    Sichuan Univ Coll Life Sci Res Ctr Analyt Instrumentat Key Lab Bioresource &

    Ecoenvironm Minist Educ Chengdu 610064 Sichuan 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

    Fluorescent aptasensor; Magnetic beads; Nicking enzyme; Ampicillin; Gold nanoparticles;

    机译:荧光aptasensor;磁珠;切口酶;氨苄青霉素;金纳米粒子;

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