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Novel 3D Printed Device for Dual-Signaling Ratiometric Photoelectrochemical Readout of Biomarker Using lambda-Exonuclease-Assisted Recycling Amplification

机译:使用λ-Exonuclease辅助回收扩增生物标志物的双信号尺定光电化学读数的新型3D印刷装置

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摘要

A ratiometric photoelectrochemical (PEC) sensing strategy was proposed for monitoring of carcinoembryonic antigen (CEA) based on a homemade 3D printing device with dual-working photoelectrodes (PE1 and PE2), coupling lambda-exonuclease (lambda-Exo)-assisted recycling amplification with CdS quantum dots. Gold nanoparticles-functionalized ZnO nanorods were utilized as PEC substrate for generating initial photocurrent and immobilizing DNA probe. Upon incubation of target with DNA trigger/CEA aptamer-modified magnetic bead (tri/apt-MB), DNA trigger dissociated from magnetic bead and then hybridized with capture probe (cp) on PE1 or opened hairpin probe (hp) on PE2 to form double-stranded DNA (dsDNA). The exonuclease could recognize and cleave two newly generated dsDNA, leading to the release of trigger. The free trigger strand continued to hybridize with the remaining cp/hp, which were cleaved by lambda-Exo, and then trigger was released again and restarted next recycle with the lambda-Exo. After digestion of lambda-Exo, the number of capture probes on PE1 was reduced, and many short DNA fragments were produced on PE2, thereby resulting in the decreasing CdS QDs on PE1 and the increasing CdS QDs on PE2. As a result, it was observed that the ratio value of photocurrents (PE1/PE2) significantly decreased with the increasing CEA. Under optimum conditions, the sensing method showed a good linear relationship toward CEA within the dynamic range of 0.02-10 ng mL(-1) and a detection limit of 6.0 pg mL(-1). Moreover, the ratiometric PEC sensor exhibited good reproducibility, satisfying stability, and remarkable anti-interference performance, which suggests its promising application prospect to detect target CEA.
机译:提出了一种基于具有双工作光电电极(PE1和PE2)的自制3D打印装置的自制3D打印装置来监测癌胚抗原(CEA)的测定的光电化学(PEC)感测策略,用CD量子点。金纳米颗粒 - 官能化ZnO纳米棒用作PEC底物,用于产生初始光电流和固定DNA探针。用DNA触发/ CEA适体改性的磁珠(TRI / APT-MB)孵育靶,DNA触发从磁珠中解离,然后用PE1上的捕获探针(CP)与PE2上的捕获探针(CP)杂交以形成双链DNA(DSDNA)。外切核酸酶可以识别并切割两个新生成的DSDNA,导致触发的释放。与剩余的Cp / HP继续杂交,通过λ-exo切割,然后再次释放触发并用λ-exo重新开始触发。在消化λ-exo后,PE1上的捕获探针的数量降低,并且在PE2上产生了许多短的DNA片段,从而导致PE1上的CDS QD和PE2上的增加CDS QDS降低。结果,观察到,随着CEA的增加,光电流(PE1 / PE2)的比率值显着降低。在最佳条件下,感测方法显示在0.02-10ng ml(-1)的动态范围内的CEA线性关系良好,检测限为6.0pg ml(-1)。此外,比率PEC传感器具有良好的再现性,满足稳定性和显着的抗干扰性能,这表明其具有检测目标CEA的有前景的应用前景。

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  • 来源
    《Analytical chemistry》 |2019年第15期|共7页
  • 作者单位

    Fuzhou Univ Dept Chem Key Lab Analyt Sci Food Safety &

    Biol MOE &

    Fujia Fuzhou 350108 Fujian Peoples R China;

    Fuzhou Univ Dept Chem Key Lab Analyt Sci Food Safety &

    Biol MOE &

    Fujia Fuzhou 350108 Fujian Peoples R China;

    Fuzhou Univ Dept Chem Key Lab Analyt Sci Food Safety &

    Biol MOE &

    Fujia Fuzhou 350108 Fujian 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;
  • 关键词

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