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Dual-mode colorimetric/photoelectrochemical sensing platform derived from the decomposition of CuHPT for glutathione
1Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Laboratory of Molecule-Based Materials, Anhui Province Key Laboratory of Biomedical Materials and Chemical Measurement, College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241000, China. kanxw@mail.ahnu.edu.cn.
Abstract:
The development of integrated dual signal outputs for the reliable and accurate determination of glutathione (GSH) is highly significant for its key role in physiological processes. Herein, a colorimetric/photoelectrochemical (PEC) dual-mode sensing platform was constructed based on the GSH-triggered decomposition of a copper-organic framework (CuHPT). A hollow nanostructured type-II heterojunction of CoS/In-CdS was synthesized using an imidazolate framework (ZIF-67) as a template. CuHPT was decomposed in the presence of GSH to form catechol ligands and Cu+, enabling dual-mode sensing. An ion exchange reaction between the produced Cu+ and Cd2+ of CoS/In-CdS resulted in the formation of Cu2S, causing a decrease in the photocurrent and the sensitive detection of GSH. Cu+ catalyzed H2O2 to produce ˙OH via a Fenton-like reaction, achieving colorimetric sensing. The proposed dual-mode sensor based on the target-triggered decomposition of CuHPT exhibited linear responses for colorimetric and PEC sensing of GSH in the range of 0.05-1.20 mM and 0.5-800 μM with the limit of detections (LODs) of 18 μM and 0.11 μM, respectively. The reliable determination of GSH in human serum provides a new possibility for the application of the present dual-mode sensor in clinical assays.
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