Issue 13, 2025

Electrochemiluminescence sensor based on Ag/ZnO nanomaterial-enhanced GPTMS/FeCdS@FeIn2S4 for sensitive analysis of CD44

Abstract

Incorporating an additional metal ion into binary metal sulfides to adjust the band gap and carrier mobility, thereby forming ternary metal sulfides, has significant potential in the field of electrochemical luminescence. This research represents the first application of FeCdS@FeIn2S4 as an innovative electrochemiluminescence (ECL) emitter. To further enhance the ECL signal, ZIF-8-derived Ag-doped ZnO nanocomposites were engineered as co-reaction accelerators, leveraging their exceptional catalytic activity to enhance the FeCdS@FeIn2S4/K2S2O8 system through efficient generation of SO4˙ radicals. A novel sandwich-type ECL immunosensor for detecting cell adhesion molecule 44 (CD44) was initially constructed. The biocompatibility of the material was enhanced through epoxy functionalization using 3-glycidyloxypropyltrimethoxysilane (GPTMS). Ag/ZnO served as a catalyst to promote the reduction of S2O82−, generating more SO4˙, which enhanced the ECL intensity and stability of GPTMS/FeCdS@FeIn2S4 under the dual influence of catalysing S2O82− decomposition and acting as an energy donor. Through the synergistic catalytic effect of Ag, the electrical conductivity and biocompatibility of the composites were enhanced, and the bandgap width of ZnO was reduced, thereby improving the electron transfer capability of Ag/ZnO. The developed immunosensor was utilized to accurately detect CD44, exhibiting a linear range of 10 fg mL−1 to 100 ng mL−1 and a detection limit of 9.16 fg mL−1.

Graphical abstract: Electrochemiluminescence sensor based on Ag/ZnO nanomaterial-enhanced GPTMS/FeCdS@FeIn2S4 for sensitive analysis of CD44

Supplementary files

Article information

Article type
Paper
Submitted
31 Mar 2025
Accepted
20 May 2025
First published
06 Jun 2025

Analyst, 2025,150, 2907-2916

Electrochemiluminescence sensor based on Ag/ZnO nanomaterial-enhanced GPTMS/FeCdS@FeIn2S4 for sensitive analysis of CD44

F. Li, Y. Wang, X. Liao, K. Liu, L. Hu, H. Ma, D. Wu and Q. Wei, Analyst, 2025, 150, 2907 DOI: 10.1039/D5AN00366K

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