4.6 Article

High-efficiency interparticle DNA walker amplifier combined with N-Ti3C2 quantum dots as electrochemiluminescence emitters for sensitive protein assay

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ELECTROCHIMICA ACTA
卷 457, 期 -, 页码 -

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2023.142479

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Electrochemiluminescence; Biosensor; DNA amplifier

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In this study, an electrochemiluminescence (ECL) biosensor based on interparticle DNA walker and N-Ti3C2 QDs was developed for sensitive assay of MUC1. The interparticle DNA walker could improve the conversion efficiency of target MUC1 by enhancing its moving freedom and area. The synthesized N-Ti3C2 QDs showed higher ECL luminous efficiency compared to previous reported N-Ti3C2 QDs, providing a potential feasible method for other protein sensitive assay.
In this work, an electrochemiluminescence (ECL) biosensor based on interparticle DNA walker as effective signal amplification strategy and N-Ti3C2 QDs as high-efficiency emitters was designed for sensitive assay of mucin 1 (MUC1), which is closely related to the occurrence and development of tumors. First, an interparticle DNA walker which contains walking particles (WPs) and orbit particles (OPs) was fabricated. In the presence of target MUC1 and DNAzyme, the WPs can walk along the surface of OPs, and they can continue to walk along next OPs after completing previous walk. As the moving freedom and area improved, the interparticle DNA walker could effectively improve the conversion efficiency of target. Furthermore, N-Ti3C2 QDs with high ECL luminous ef-ficiency were synthesized by using polyethyleneimine (PEI) as nitrogen source. Due to the nitrogen-rich of PEI, the relative ECL quantum efficiency of the proposed N-Ti3C2 QDs was calculated to be 1.5 times higher than our previous reported N-Ti3C2 QDs that utilizing ethylenediamine as nitrogen source. Therefore, taking the advan-tage of the improved moving freedom and area of the interparticle DNA walker and high ECL efficiency of the proposed N-Ti3C2 QDs, the fabricated ECL biosensor for MUC1 determination displayed a low detection limit with a wide linear range, which provides a potential feasible method for other protein sensitive assay.

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