Ultrasensitive and versatile homogeneous electrochemical cytosensing platform based on target-induced displacement reaction for "signal-on" bioassay

被引:12
作者
Gu, Chengcheng [1 ]
Gai, Panpan [1 ]
Liu, Xiaojuan [1 ]
Liu, Jing [2 ]
Li, Feng [1 ]
机构
[1] Qingdao Agr Univ, Coll Chem & Pharmaceut Sci, Qingdao 266109, Peoples R China
[2] Qingdao Agr Univ, Cent Lab, Qingdao 266109, Peoples R China
基金
中国国家自然科学基金;
关键词
Homogeneous electrochemical cytosensing platform; Target induced displacement reaction; Signal on assay; Tumor cell detection; IMMOBILIZATION-FREE; ACTIVITY ASSAY; CARGO RELEASE; DNA; CELL; AMPLIFICATION; CANCER; MICRORNA; STRATEGY; ELECTROCHEMILUMINESCENCE;
D O I
10.1016/j.snb.2018.04.167
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We proposed, for the first time, a ultrasensitive amplification-free, label-free, and enzyme-free homogeneous electrochemical cytosensing platform based on the target-induced displacement reaction for tumor cell "signal-on" assay. To realize this proposal, the electroactive probe, [Fe(CN)(6)](3-), was entrapped in the pores of positively charged MSN (PMSN), and then the negatively charged aptamer of the tumor cell was adsorbed on the surface of PMSN as a biogate. Once the tumor cells were recognized and captured by the aptamer, the biogate could be efficiently opened and the entrapped [Fe(CN)(6)](3-) released, which can be ascribed to the decreased adhesion between the aptamer-cell complex and PMSN. Consequently, the electrochemical signal dramatically increased. Overall, the "signal-on" strategy was conveniently realized. Notably, the detection limit for tumor cells assay (13 cells/mL) is comparable to those of the reported methods Furthermore, based on the similar proposal, this biosensor also can be extended for the ultrasensitive detection of microRNA (38 aM, SIN = 3) and Hg2+ (0.47 pM, S/N = 3). Therefore, this biosensing platform has the great potential to be a powerful tool in the applications of disease diagnostics and environmental monitoring. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
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