Near infrared imaging of intracellular GSH by AuNCs@MnO2 core–shell nanoparticles based on the absorption competition mechanism. Issue 16 (16th July 2021)

• Record Type: Journal Article
• Authors: Yao, Haiyang; Jiang, Difei; Dong, Gaoqiu; Sun, Jiamin; Sun, Shasha; Li, Lingling; Zheng, Fenfen; Xiong, Weiwei
• Is Part Of: Analyst. Volume 146:Issue 16(2021)
• Page Start: 5115
• Page End: 5123
• Publication Date: 2021-07-16
• Subjects: Chemistry, Analytic -- Periodicals; 543
• DOI: 10.1039/d1an00839k
• Languages: English
• ISSNs: 0003-2654

Abstract

Abstract : AuNCs@MnO2 core–shell nanoprobes for NIR fluorescence imaging of intracellular GSH based on the absorption competition mechanism. Abstract : Dynamically monitoring intracellular glutathione (GSH), a crucial biomarker of oxidative stress, is of significance for the diagnosis and treatment of certain diseases. Although manganese dioxide (MnO2 ) based GSH fluorescent sensors have exhibited high sensitivity and good selectivity owing to the specific reactivity between GSH and MnO2, near-infrared (NIR) MnO2 based nanoprobes for GSH detection are scarce. Herein, we have developed a NIR activatable fluorescence nanoprobe for the imaging and determination of intracellular GSH based on a core–shell nanoparticle, consisting of NIR emitted gold nanocluster doped silica as the fluorescent core and manganese dioxide as the GSH-responsive shell (named AuNCs@MnO2 ). Due to the absorption competition mechanism, the outer MnO2 shell rather than the inner AuNCs core preferentially absorbed the excitation light, thus leading to fluorescence quenching of the inner AuNCs core. Upon addition of GSH, the fluorescence of the nanoprobe restored along with the reduction of MnO2 to Mn 2+ because of the absorption competition disappearance-induced emission. The activatable fluorescence linearly increased upon changing the GSH concentration in the range of 2 to 5000 μM with a detection limit of 0.67 μM. The cytotoxicity test shows that the AuNCs@MnO2 nanoprobes have a good biocompatibility. After entering the cancer cells, the intracellular GSH degraded the outermost MnO2 shell and initiated the NIR fluorescence restoration of AuNCs, which can be used to monitor the dynamic change of intracellular GSH. This strategy provides an NIR-activatable way to detect GSH levels in living cells and offers a promising platform for the diagnosis and treatment of GSH-related diseases.