A fluorescence sensing platform with the MnO2 nanosheets as an effective oxidant for glutathione detection

被引:44
|
作者
Yao, Cuiping [1 ]
Wang, Jing [1 ]
Zheng, Aixian [2 ,3 ]
Wu, Lingjie [2 ,3 ]
Zhang, Xiaolong [2 ,3 ]
Liu, Xiaolong [2 ,3 ]
机构
[1] Xi An Jiao Tong Univ, Inst Biomed Analyt Technol & Instrumentat, Sch Life Sci & Technol, Key Lab Biomed Informat Engn,Minist Educ, Xian 710049, Shaanxi, Peoples R China
[2] Fujian Med Univ, United Innovat Mengchao Hepatobiliary Technol Key, Mengchao Hepatobiliary Hosp, Fuzhou 350025, Fujian, Peoples R China
[3] Fujian Med Univ, Liver Ctr Fujian Prov, Fuzhou 350025, Fujian, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Glutathione; Manganese dioxide nanosheets; O-phenylenediamine; Redox reaction; Oxidation; CELLULAR GLUTATHIONE; PROBE; BIOTHIOLS; NANOPARTICLES; THIOLS; ENZYME; ASSAY;
D O I
10.1016/j.snb.2017.05.136
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein, a sensitive, selective, rapid and cost-effective fluorescence sensing platform has been designed for the detection of glutathione (GSH). In this platform, the manganese dioxide (Mn0(2))nanosheets served as both oxidant, which could effectively oxidize o-phenylenediamine (OPDA) to produce fluorescence for highly sensitive detection, and recognition element. When GSH was introduced, the Mn02 nanosheets were reduced to Mn2+, which inhibited the formation of fluorescent oxidation products of OPDA. Under optimal conditions, the Mn0(2)-OPDA sensing platform showed very sensitive response to GSH in the range of 10 nM-40 mu M. The detection limit of GSH reached as low as 10 nM. The high selectivity of inhibition of fluorescent product formation by GSH allows this platform to be used for detecting GSH in practical biological samples (such as cell extracts). (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:30 / 36
页数:7
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