4.7 Article

An electrochemical aptasensor for Mycobacterium tuberculosis ESAT-6 antigen detection using bimetallic organic framework

期刊

MICROCHIMICA ACTA
卷 188, 期 11, 页码 -

出版社

SPRINGER WIEN
DOI: 10.1007/s00604-021-05058-8

关键词

Tuberculosis; Bimetallic organic framework; Nitrogen-doped graphene; Electrochemical aptasensor; Cyclic voltammetry

资金

  1. National Natural Science Foundation of China [82072378, 81601856]
  2. Chongqing Talent Program, China [CQYC202005015]
  3. Ba Yu Scholar Program, China [YS2019020]
  4. Funds for High Level Young Science and Technology Talent Cultivation Plan in Chongqing Medical University, China (2019)
  5. Discipline Talent Training Program of College of Pharmacy in Chongqing Medical University, China [YXY2019XSGG4]
  6. Funds for Young Science and Technology Talent Cultivation Plan of Chongqing City [cstc2014kjrc-qnrc00004]

向作者/读者索取更多资源

In this study, a label-free electrochemical aptasensor based on a bimetallic organic framework nanohybrid was developed for sensitive detection of ESAT-6. The nanohybrid exhibited excellent electrochemical response and could be directly used for anchoring ESAT-6 binding aptamers. The aptasensor showed a wide linear range, low limit of detection, good reproducibility, and promising results in real sample analysis, demonstrating its potential as a diagnostic tool for tuberculosis in clinical practice.
A label-free electrochemical aptasensor is reported for sensitive detection of the 6-kDa early secreted antigenic target (ESAT-6). For the first time, the bimetallic organic framework (b-MOF) of Zr-MOF-on-Ce-MOF was decorated with nitrogen-doped graphene (NG) and applied as the matrix for electroactive toluidine blue (Tb) to form the NG@Zr-MOF-on-Ce-MOF@Tb nanohybrid. The prepared nanohybrid with excellent hydrophilicity, dispersibility, and large specific surface exhibited significant electrochemical response. This nanohybrid could be directly used for anchoring ESAT-6 binding aptamers (EBA) through the interaction between the 5'-phosphate group (PO43-) of EBA and Zr4+ of Zr-MOF. The signal response before and after incubating the ESAT-6 antigen has been evaluated by cyclic voltammetry at a scan rate of 100 mV s(-1) from - 0.7 to 0.3 V (vs. SCE). Under optimal conditions, the proposed aptasensor displayed a wide linear range from 100 fg mL(-1) to 10 ng mL(-1) with a limit of detection (LOD) of 12 fg mL(-1). The developed method showed good reproducibility with a relative standard deviation (RSD) of 2.27%. The aptasensor showed favorable results in the analysis of the real samples. With these merits, the aptasensor has exceptional potential as a diagnostic tool for tuberculosis in clinical practice.

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