β-Cyclodextrin-functionalized Ti3C2Tx MXene nanohybrids as innovative signal amplifiers for the electrochemical sandwich-like immunosensing of squamous cell carcinoma antigen

被引:6
作者
Jiang, Yuling [2 ]
Yang, Miao [1 ]
Yu, Mingyao [4 ]
Huang, Lingling [3 ]
Ke, Yue [1 ]
Yang, Lei [1 ]
机构
[1] Hubei Univ Arts & Sci, Xiangyang Cent Hosp, Affiliated Hosp, Dept Stomatol, Xiangyang 441000, Peoples R China
[2] Hubei Univ Med, Xiangyang No Peoples Hosp 1, Dept Stomatol, Xiangyang 441053, Peoples R China
[3] Fujian Med Univ, Affiliated Hosp 1, Dept Stomatol, Fuzhou 350001, Peoples R China
[4] Xiangyang Polytech, Dept Oral Med, Xiangyang 441006, Peoples R China
关键词
PHOTOELECTROCHEMICAL IMMUNOSENSOR; IONIC LIQUID; PLATFORM; SENSOR;
D O I
10.1039/d2ay01716d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein, a simple and highly sensitive electrochemical sandwich-like immunosensor for the squamous cell carcinoma antigen (SCCA) was constructed using gold nanoparticle/graphene nanosheet (Au/GN) nanohybrids as a sensing platform and beta-cyclodextrin/Ti3C2Tx MXenes (beta-CD/Ti3C2Tx) as a signal amplifier. The good biocompatibility and large surface area as well as the high conductivity of Au/GN allow the platform to load primary antibodies (Ab(1)) and facilitate electron transport. In the case of the beta-CD/Ti3C2Tx nanohybrids, the beta-CD molecule is dedicated to binding secondary antibodies (Ab(2)) through host-guest interactions, thus inducing the formation of the sandwich-like structure Ab(2)-beta-CD/Ti3C2Tx/SCCA/Ab(1)/Au/GN in the presence of SCCA. Interestingly, Cu2+ can be adsorbed and self-reduced on the surface of the sandwich-like structure to form Cu-0 since Ti3C2Tx MXenes can exhibit superior adsorption and reduction capabilities towards Cu2+, and a prominent current signal of Cu-0 can be observed via differential pulse voltammetry. Based on this principle, an innovative signal amplification strategy has been proposed for SCCA detection, which avoids the process of labeling the probe and the specific immobilization step of catalytic components on the surface of amplification markers. After the optimization of various conditions, a wide linear range from 0.05 pg mL(-1) to 20.0 ng mL(-1), coupled with a low detection limit of 0.01 pg mL(-1), was obtained for SCCA analysis. The proposed method for SCCA detection was also applied in real human serum samples and the observed results are satisfactory. This work opens up new pathways for constructing electrochemical sandwich-like immunosensors for SCCA and other targets.
引用
收藏
页码:1336 / 1344
页数:9
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