4.7 Article

Competitive electrochemiluminescence aptasensor based on the Ru(II) derivative utilizing intramolecular ECL emission for E2 detection

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 348, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2021.130717

关键词

Intramolecular electrochemiluminescence; Competitive; Aptasensor; Ru(dcbpy)(3)(2+); Carbohydrazide

资金

  1. National Key Scientific Instrument and Equipment Development Project of China [21627809]
  2. National Natural Science Foundation of China [21607055, 21775053, 21777056]
  3. Natural Science Foundation of Shandong Province [2019GSF111023]
  4. Innovation Team Project of Colleges and Universities in Jinan [2019GXRC027]
  5. Jinan Scientific Research Leader Workshop Project [2018GXRC024]

向作者/读者索取更多资源

This study investigated a competitive aptasensor for ultrasensitive detection of E-2 based on a novel intramolecular ECL emission system. By optimizing the Ru(II) derivatives and designing heterostructures as reaction accelerators, stronger ECL signals and further amplification effects were achieved in the detection of E-2.
One competitive aptasensor based on novel intramolecular ECL emission system was investigated for ultrasensitive detection of E-2. It should be noted that the Ru(II) derivative for the mechanism of intramolecular ECL could improve electron transfer efficiency and reduce energy consumption. The Ru(II) derivatives were prepared by optimizing distribution ratio of Ru(dcbpy)(3)(2+) and carbohydrazide for acquiring the ECL signal maximum. Stimulated by In3+/In+ redox reversible electron pair in the InVO4/beta-AgVO3 heterostructures, the InVO4/beta-AgVO3 heterostructures were designed as co-reaction accelerator to expedite ECL emission reaction between CON4H6. and Ru(dcbpy)(3)(3+). Taking advantage of associative competition between cDNA and E-2 with aptamer, the ECL signal realized further amplification. The specific binding of the aptamer to E-2, was stronger than that to the cDNA by hybridization. A mass of Ru(II) derivatives could adsorb and embed into the hybridized double stranded DNA to immobilize on the electrode surface and generate satisfactory ECL signal. The specific binding of the aptamer to E-2 decreased the cDNA content on electrode surface, which contributed to lessen the adsorption amount of Ru(dcbpy)(3)(2+) and distinctly affected the ECL signal. Under optimal conditions, the proposed biosensor provided an admirable linearity to the level of E-2 between 0.001 nmol/L and 100 nmol/L with a low detection limit of 0.27 pmol/L. The proposed aptasensor not only stimulates more interest in the mechanism of intramolecular ECL but also has towardly development potential for constructing competitive strategies.

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