分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

Electrochemiluminescence immunosensor for cancer antigen 125 detection based on novel resonance energy transfer between graphitic carbon nitride and NIR CdTe/CdS QDs

Hongmin Gao, Ze Zhang, Yingcong Zhang, Hongwei Yu, Shengzhong Rong, Lingqiang Meng, Shizhen Song, Yong Mei, Hongzhi Pan, Dong Chang

Journal:JOURNAL OF ELECTROANALYTICAL CHEMISTRY

IF:4.46

DOI:10.1016/j.jelechem.2021.115104

PMID:

Published:2021-03-09

research field:神经科学分子生物学遗传学发育生物学表观遗传学

Abstract

Resonance energy transfer (RET), as an efficient strategy, has been widely used for exploring a variety of biological processes and achieving sensitive bioanalysis. In this work, fluorescence and electrochemiluminescence (ECL) RET between graphitic carbon nitride (g-C 3 N 4 ) and NIR CdTe/CdS QDs was reported firstly. Based on this novel RET system, a sensitive sandwich-type ECL immunosensor was constructed to detect cancer antigen 125 (CA125). In this strategy, the ECL of Au NPs-functionalized graphitic carbon nitride nanohybrids (Au-g-C 3 N 4 NHs) was efficiently quenched by near-infrared CdTe/CdS quantum dots (NIR CdTe/CdS QDs), where NIR CdTe/CdS QDs acts as acceptors, and Au-g-C 3 N 4 NHs acts as donors. Au NPs improved the intensity and stability of ECL and provided sites to immobilize the antibody. Silica nanospheres carried abundant NIR CdTe/CdS QDs (QDs-SiO 2 ) labeling secondary antibodies, further enhancing the quenching effect. Under the optimum conditions, the constructed immunosensor showed excellent analytical performance with a linear concentration of CA125 from 0.0001 U mL −1 to 10 U mL −1 and the limit of detection reached 0.034 mU mL −1 (S/N = 3). Meanwhile, the immunosensor also revealed great stability, reproducibility, and selectivity and it could be applied in human serum samples successfully. This strategy provided a useful analytical method for the sensitive detection of biomarkers in the early stages of the disease and an innovative reference for developing more efficient and sensitive RET bioanalysis.

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