4.6 Article

Exciton-Plasmon Interactions between CdS@g-C3N4 Heterojunction and Au@Ag Nanoparticles Coupled with DNAase-Triggered Signal Amplification: Toward Highly Sensitive Photoelectrochemical Bioanalysis of MicroRNA

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 5, 期 11, 页码 10840-10848

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.7b02774

关键词

Photoelectrochemistry; MicroRNA-21; Enzyme-assisted cycle amplification; Exciton-plasmon interactions; Heterojunction

资金

  1. National Natural Science Foundation of China [21675136, 21375114, 21405129]
  2. Plan for Scientific Innovation Talent of Henan Province [2017JR0016]
  3. Funding Scheme for the Young Backbone Teachers of Higher Education Institutions in Henan Province [2016GGJS-097]
  4. Nanhu Young Scholar Supporting Program of XYNU

向作者/读者索取更多资源

Novel exciton-plasmon interactions (EPI) between CdS@g-C3N4 heterojunction and Au@Ag nanoparticles (NPs) was introduced for the first time into the photoelectrochemical (PEC) biosensing system for highly sensitive microRNA-21 detection using duplex-specific nuclease assisted cycle amplification for sensitivity enhancement. The photo electrode of CdS@g-C3N4, nanowires could generate a great photocurrent because of the formation of the p-n heterojunction. Due to the natural absorption overlap, the exciton of CdS@g-C3N4 and the plasmon of Au@Ag NPs could be induced simultaneously to form EPI. Specifically, the perfect overlap of the wide absorption spectrum of Au@Ag NPs with the photoluminescence spectrum of CdS@g-C3N4 allows the resonance energy transfer and EPI between CdS@g-C3N4 nanowire and Au@Ag NPs simultaneously. The effective EPI renders the signal change modulated by the interparticle distance significantly. Such a signaling mechanism was then used to biosensor for microRNA-21 detection, within which the duplex-specific nuclease (DSN) was further introduced to enhance the sensitivity. The constructed PEC biosensor exhibits the sub-fM level (0.05 fM) detection of microRNA-21 with a wide range from 0.1 fM to 1.0 nM. In complex biological samples, the proposed method also possesses good specificity, reproducibility, and stability.

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