Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, the Chinese Academy of Sciences (CAS) , Beijing 100190, China.
Anal Chem. 2014 Dec 16;86(24):12206-13. doi: 10.1021/ac503215z. Epub 2014 Nov 25.
In this study, we systematically investigate the mechanism of single-layer MnO2 nanosheets suppressing fluorescence of 7-hydroxycoumarin and, based on this, demonstrate a new fluorescent method for in vivo sensing of ascorbic acid (AA) in rat brain. The mechanism for the fluorescence suppression is attributed to a combination of inner filter effect (IFE) and static quenching effect (SQE), which is different from those reported for the traditional two-dimensional nanosheets, and Förster resonant energy transfer (FRET) mechanism reported for MnO2 nanosheets. The combination of IFE and SQE leads to an exponential decay in fluorescence intensity of 7-hydroxycoumarin with increasing concentration of MnO2 nanosheets in solution. Such a property allows optimization of the concentration of MnO2 nanosheets in such a way that the addition of reductive analyte (e.g., AA) will to the greatest extent restore the MnO2 nanosheets-suppressed fluorescence of 7-hydroxycoumarin through the redox reaction between AA and MnO2 nanosheets. On the basis of this feature, we demonstrate a fluorescent method for in vivo sensing of AA in the cerebral systems with an improved sensitivity. Compared with the turn-on fluorescent method through first decreasing the fluorescence to the lowest level by adding concentrated MnO2 nanosheets, the method demonstrated here possesses a higher sensitivity, lower limit of detection, and wider linear range. Upon the use of ascorbate oxidase to achieve the selectivity for AA, the turn-on fluorescence method demonstrated here can be used for in vivo sensing of AA in a simple but reliable way.
在这项研究中,我们系统地研究了单层 MnO2 纳米片抑制 7-羟基香豆素荧光的机制,并基于此,展示了一种新的用于在体检测大鼠脑内抗坏血酸(AA)的荧光方法。荧光抑制的机制归因于内滤效应(IFE)和静态猝灭效应(SQE)的结合,这与传统二维纳米片的机制不同,也不同于 MnO2 纳米片的Förster 共振能量转移(FRET)机制。IFE 和 SQE 的结合导致 7-羟基香豆素的荧光强度随溶液中 MnO2 纳米片浓度的增加呈指数衰减。这种特性使得可以优化 MnO2 纳米片的浓度,从而通过 AA 和 MnO2 纳米片之间的氧化还原反应,最大程度地恢复 MnO2 纳米片抑制的 7-羟基香豆素的荧光。基于这一特性,我们展示了一种用于在体检测大脑系统中 AA 的荧光方法,其灵敏度得到了提高。与通过添加浓 MnO2 纳米片将荧光降至最低水平的开荧光方法相比,本文所展示的方法具有更高的灵敏度、更低的检测限和更宽的线性范围。通过使用抗坏血酸氧化酶实现 AA 的选择性,本文所展示的开荧光方法可以用于简单但可靠的在体检测 AA。