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Hierarchical Au nanoarrays functionalized 2D TiCT MXene membranes for the detection of exosomes isolated from human lung carcinoma cells. | LitMetric

Hierarchical Au nanoarrays functionalized 2D TiCT MXene membranes for the detection of exosomes isolated from human lung carcinoma cells.

Biosens Bioelectron

School of Biomedical Engineering (Suzhou), Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230026, PR China; Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Science, Suzhou, 215163, PR China. Electronic address: wenfeidong@s

Published: November 2022


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Article Abstract

Exosome is considered an important biomarker of liquid biopsy in early cancer screening, which can reflect the physiological and pathological status of cancer cells. Herein, we construct a novel electrochemical biosensor based on hierarchical Au nanoarray-modified 2D TiCT MXene membranes for sensitive detection of exosomes. TiCT MXene nanosheets were fabricated as the building blocks for preparing 2D membranes as the sensing platform via vacuum filtration. To enhance the conductivity of the MXene membrane, for the first time, hierarchical Au nanoarrays were further deposited in situ on the MXene membrane surface. The combination of MXene membrane with a large specific area and hierarchical Au nanoarrays with excellent conductivity make higher electrocatalytic and more active sites in aptamer immobilization. In this strategy, the composite membrane modified by EpCAM recognized aptamer can specifically capture target exosomes, meanwhile, these target exosomes anchor aptamer for CD63 to further enhance the sensing sensitivity and accuracy of the biosensor. As a result, the biosensor achieved high sensitivity and reliable performance for exosome sensing, with a low detection limit (58 particles/μL) in the linear range of 1 × 10 to 1 × 10 particles/μL. In addition, this biosensor showed satisfactory electrochemical stability and anti-interference ability for the detection of exosomes in real serum samples.

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http://dx.doi.org/10.1016/j.bios.2022.114647DOI Listing

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