Label-free electrochemical detection of HepG2 tumor cells with a self-assembled DNA nanostructure-based aptasensor

[Display omitted] •Aptasensor was developed for the electrochemical detection and release of CTCs.•Tetrahedron-based aptamer was used for the highly enhanced capture of target cells.•Dendritic structure nanoprobes amplified the electrochemical signals significantly.•The detection limit of the cytose...

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Veröffentlicht in:Sensors and actuators. B, Chemical Chemical, 2018-09, Vol.268, p.359-367
Hauptverfasser: Sun, Duanping, Lu, Jing, Chen, Dabin, Jiang, Yunfei, Wang, Zhiru, Qin, Weiwei, Yu, Yanyan, Chen, Zuanguang, Zhang, Yuanqing
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Sprache:eng
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Zusammenfassung:[Display omitted] •Aptasensor was developed for the electrochemical detection and release of CTCs.•Tetrahedron-based aptamer was used for the highly enhanced capture of target cells.•Dendritic structure nanoprobes amplified the electrochemical signals significantly.•The detection limit of the cytosensor could be estimated as 5 cells mL−1 for HepG2.•This method released the captured HepG2 cells with little damage for further study. The development of rapid, sensitive and convenient methods for the monitoring of rare circulating tumor cells (CTCs) is of great significance in cancer diagnostics and therapy. Herein a label-free and competitive electrochemical aptasensor was proposed for the efficient capture, ultrasensitive detection and controlled release of CTCs. Firstly, the DNA nanotetrahedron (NTH)-based TLS11a aptamer probe was immobilized on a disposable screen-printed gold electrode (SPGE) surface via the Au−S bonds for the highly enhanced capture of liver cancer HepG2 cells. Then, hybrid nanoprobes of Pd-Pt nanocages labeled with complementary DNA (cDNA), hemin/G-quadruplex DNAzyme and horseradish peroxidase (HRP) were attached on the SPGE substrate by the DNA hybridization, resulting in the formation of dendritic structure (DS) nanoprobes with self-assembly methods for the greatly enhanced sensitivity. When the target HepG2 cells existed, they can compete with DS nanoprobes to bind with NTH-based aptamer probe, resulting in the release of the DS nanoprobes from the SPGE. This method exhibits ultrahigh selectivity and sensitivity toward HepG2 with detection limits of 5 cells per ml. Furthermore, our strategy allows for easy detachment of the captured cells from the SPGE without compromising cell viability by an electrochemical cleavage of the Au–S bonds. The present study provides a label-free technique for highly selective and efficient quantification of tumor cells, which is essential in the early cancer diagnosis and treatment of cancer.
ISSN:0925-4005
1873-3077
DOI:10.1016/j.snb.2018.04.142