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Label-Free and Ultrasensitive Electrochemiluminescent Immunosensor Based on Novel Luminophores of Ce<sub>2</sub>Sn<sub>2</sub>O<sub>7</sub> Nanocubes

Malik Saddam KhanMOE Key Laboratory of Analytical Science of Food Safety and Biology, Fujian Provincial Key Laboratory of Analysis and Detection for Food Safety, and College of Chemistry, Fuzhou University, Fuzhou 350108, P. R. ChinaHafsa AmeerMOE Key Laboratory of Analytical Science of Food Safety and Biology, Fujian Provincial Key Laboratory of Analysis and Detection for Food Safety, and College of Chemistry, Fuzhou University, Fuzhou 350108, P. R. ChinaYuwu ChiMOE Key Laboratory of Analytical Science of Food Safety and Biology, Fujian Provincial Key Laboratory of Analysis and Detection for Food Safety, and College of Chemistry, Fuzhou University, Fuzhou 350108, P. R. China
2021en
ABI

Abstract

In this research article, a novel and simple label-free electrochemiluminescence (ECL) immunosensor using cerium stannite (Ce2Sn2O7) nanocubes as brand-new ECL emitters has been suggested for the first time. Ce2Sn2O7 nanocubes prepared by a simple hydrothermal method displayed bright ECL emission, promising biocompatibility, low noxiousness, and perfect stability. On comparison of ECL and photoluminescence (PL) spectra, a surface-state mechanism was proposed to be involved in the ECL emission. After aminofunctionalization with 3-aminopropyltriethoxysilane (APTES), Ce2Sn2O7 could be decorated with gold nanoparticles through Au–NH2 covalent linkage, which yielded Au@Ce2Sn2O7 nanocomposites and further enhanced the ECL emission. To confirm the proposed immunosensor feasibility, carcinoembryonic antigen (CEA) was employed as an exemplary analyte. Based on the abovementioned points, our fabricated immunosensor improved the ECL performance to CEA concentrations in a linear range of 0.001–70 ng/mL with a low limit of detection of 0.53 pg/mL (S/N = 3). With outstanding stability, reproducibility, and specificity, this method is expected to be an innovative one for sensitive analyses of CEA and other biomarkers in real samples.

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