4.8 Article

A Target-Driven Self-Feedback Paper-Based Photoelectrochemical Sensing Platform for Ultrasensitive Detection of Ochratoxin A with an In2S3/WO3 Heterojunction Structure

期刊

ANALYTICAL CHEMISTRY
卷 94, 期 3, 页码 1705-1712

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.1c04259

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资金

  1. Taishan Scholars Program
  2. Case-by-Case Project for Top Outstanding Talents of Jinan
  3. National Natural Science Foundation of China [21874055]
  4. Excellent Youth Innovation Team in Universities of Shandong [2019KJC016]
  5. project of 20 items of University of Jinan [2018GXRC001]

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In this study, a paper-based photoelectrochemical (PEC) sensor was developed for ultrasensitive detection of OTA. By using polyvinylpyrrolidone-treated In2S3/WO3 functionalized paper as a signal transducer and employing the Exo III-assisted cycling process and PECCC redox cycling strategy, the sensor achieved high sensitivity in OTA detection.
Currently, developing versatile, easy-to-operate, and effective signal amplification strategies hold great promise in photoelectrochemical (PEC) biosensing. Herein, an ultrasensitive polyvinylpyrrolidone-treated In2S3/WO3 (In2S3-P/WO3)-functionalized paper-based PEC sensor was established for sensing ochratoxin A (OTA) based on a target-driven self-feedback (TDSF) mechanism enabled by a dual cycling tactic of PEC chemical-chemical (PECCC) redox and exonuclease III (Exo III)-assisted complementary DNA. The In2S3-P/WO3 heterojunction structure with 3D open-structure and regulable topology was initially in situ grown on Au nanoparticle-functionalized cellulose paper, which was served as a universal signal transducer to directly record photocurrent signals without complicated electrode modification, endowing the paper chip with admirable anti-interference ability and unexceptionable photoelectric conversion efficiency. With the assistance of Exo III-assisted cycling process, a trace amount of OTA could trigger substantial signal reporter ascorbic acid (AA) generated by the enzymatic catalysis of alkaline phosphatase, which could effectively provoke the PECCC redox cycling among the tris(2-carboxyethyl)phosphine acid, AA, and ferrocenecarboxylic at the In2S3-P/WO3 photoelectrode, initiating TDSF signal amplification. Based on the TDSF process induced by the Exo III-assisted recycling and PECCC redox cycling strategy, the developed paper-based PEC biosensor realized ultrasensitive determination of OTA with persuasive selectivity, high stability, and excellent reproducibility. It is believed that the proposed paper-based PEC sensing platform exhibited enormous potential for the detection of other targets in bioanalysis and clinical diagnosis.

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