Dual mode assay of glutathione with Tb-doped g-C3N4/MnO2 nanoconjugates as fluorescence probe and Mn as elemental target

被引:10
作者
Sun, Qi-Xuan [1 ]
Zhang, Shang-Qing [1 ]
Wei, Xing [1 ]
Yang, Ting [1 ]
Wang, Jian-Hua [1 ]
Chen, Ming-Li [1 ]
机构
[1] Northeastern Univ, Coll Sci, Res Ctr Analyt Sci, Dept Chem, Shenyang 110819, Peoples R China
基金
中国国家自然科学基金;
关键词
Glutathione; MnO2; ICP-MS; Dual mode assay; Tb; PLASMA-MASS SPECTROMETRY; PLATFORM; SENSOR;
D O I
10.1016/j.aca.2022.340100
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Glutathione (GSH) plays important roles in various physiological processes, thus highly sensitive assay of GSH and timely warning of its variation at trace level in complex biological matrixes is of great significance. However, this is challenging due to the coexisting reductive biomolecules and dynamic change of GSH levels in responding to various stimuli which remain largely unexploited. Herein, we report a dual mode protocol for the assay of GSH based on nanoconjugate g-C3N4:Tb/MnO2 between MnO2 nanosheets and terbium-doped g-C3N4 (g-C3N4:Tb) nanosheets. MnO2 moiety effectively quenches the emission at 546 nm from Tb3+ in the nanoconjugate, which is restored under the reduction of MnO2 by GSH to ensure fluorescence turn-on assay of GSH. Meanwhile, the generated Mn2+ facilitates inductively coupled plasma mass spectrometry (ICP-MS) detection to endow indirect highly sensitive assay of GSH. Fluorescence mode derived a limit of detection (LOD) of 0.17 mu mol L-1 within a linear range of 0.5-160 mu mol L-1, while ICP-MS resulted in a superior LOD of 0.016 mu mol L-1 within 0.05-160 mu mol L-1. Both detection modes provide excellent selectivity to GSH. The dual mode platform was validated by GSH assay in cell lysates. It was further demonstrated by monitoring the variation of dynamic change of GSH level under CuSO4 or cisplatin induced GSH consumption.
引用
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页数:7
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