4.8 Article

Fabrication of a Polyvalent Aptamer Network on an Electrode Surface for Capture and Analysis of Circulating Tumor Cells

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ANALYTICAL CHEMISTRY
卷 -, 期 -, 页码 -

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AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.2c02778

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  1. National Natural Science Foundation of China [81772593]
  2. Fundamental Research Funds for the Central Universities [14380163]

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In this study, a strategy for capturing circulating tumor cells (CTCs) was proposed using a polyvalent aptamer network and tetrahedral DNA structures to enhance capture efficiency. The electrochemical signal generated by this method can sensitively analyze CTCs. The strategy exhibited excellent stability and anti-interference in human whole blood, showing promising potential for clinical diagnosis.
Capture and analysis of circulating tumor cells (CTCs) from complex matrixes is pivotal for the prediction of cancer metastasis and personalized treatment of cancer. Herein, we propose a strategy for CTC capture by design and fabrication of a polyvalent aptamer network on an electrode surface, which can be further used for the sensitive analysis of CTCs. In our design, the polyvalent aptamer network, which is constructed via a rolling circle amplification reaction, can significantly enhance the cell-binding abilities. Meanwhile, tetrahedral DNA structures previously assembled on the electrode surface will promote the spatial orientation and reduce the steric hindrance effect of the cell capture, thus improving the cell capture efficiency. Importantly, a detectable electrochemical signal can be obtained without additional signal probes by means of target-induced allostery of the DNA hairpin structures. Further studies reveal that the electrochemical response is proportional to the logarithm of the CTC abundance ranging from 10(2) to 5 x 10(4) cell mL(-1 )with a low limit of detection of 23 cell mL(-1). Moreover, the proposed capture strategy exhibits excellent stability and anti-interference in human whole blood, indicating its promising potential in clinical diagnosis.

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