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单层 MnO2 纳米片猝灭 7-羟基香豆素的荧光:机制研究及其在体内抗坏血酸灵敏检测中的应用。

Single-layer MnO2 nanosheets suppressed fluorescence of 7-hydroxycoumarin: mechanistic study and application for sensitive sensing of ascorbic acid in vivo.

机构信息

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.

出版信息

Anal Chem. 2014 Dec 16;86(24):12206-13. doi: 10.1021/ac503215z. Epub 2014 Nov 25.

Abstract

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.

摘要

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。

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