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支化聚乙烯亚胺功能化碳点作为一种通过关闭-开启机制对 N-乙酰半胱氨酸进行高灵敏和选择性荧光检测的探针。

Branched polyethylenimine-functionalized carbon dots as sensitive and selective fluorescent probes for N-acetylcysteine via an off-on mechanism.

机构信息

Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Pharmaceutical Sciences, Southwest University, Chongqing 400716, China.

出版信息

Analyst. 2017 Nov 6;142(22):4221-4227. doi: 10.1039/c7an01136a.

Abstract

N-Acetylcysteine (NAC) plays an important role in optimizing the protective ability of cells as well as in the treatment of some chronic clinical conditions. Unfortunately, current methods for determining NAC based on fluorescence assay strategies remain poorly investigated. In this study, a new fluorescence method for highly sensitive and selective detection of NAC was developed. The detection method employed the fluorescence (FL) signal of branched polyethylenimine-functionalized carbon dots (PEI-CDs) via an off-on mechanism. The detection system was based on the formation of cupric amine complexes by the reaction of Cu ions with surface amino groups on PEI-CDs. The FL of PEI-CDs at 460.0 nm upon exciting at 360.0 nm was quenched as a result of electron transfer between the complexes and PEI-CDs. Upon addition of NAC to Cu-CD solution, electron transfer occurred from the mercapto group on NAC to Cu, leading to the formation of Cu species and the dissociation of cupric amine complexes. As a result, the FL signal of PEI-CDs was turned on since single excited electrons cannot be transferred from PEI-CDs to the cupric amine complexes. The detection limit of this method was 0.56 μM, while the linear response ranged from 5.56 μM to 277.8 μM.

摘要

N-乙酰半胱氨酸(NAC)在优化细胞的保护能力以及治疗某些慢性临床病症方面起着重要作用。不幸的是,目前基于荧光分析策略来测定 NAC 的方法仍未得到充分研究。在本研究中,开发了一种新的荧光法来高灵敏度和选择性地检测 NAC。该检测方法利用了支化聚乙烯亚胺功能化碳点(PEI-CDs)的荧光(FL)信号,通过开-关机制。检测系统基于 Cu 离子与 PEI-CDs 表面氨基之间的反应形成铜胺配合物。在激发波长为 360.0nm 时,PEI-CDs 在 460.0nm 处的 FL 由于配合物和 PEI-CDs 之间的电子转移而被猝灭。当向 Cu-CD 溶液中加入 NAC 时,电子从 NAC 的巯基转移到 Cu 上,导致 Cu 物种的形成和铜胺配合物的解离。因此,由于单重激发电子不能从 PEI-CDs 转移到铜胺配合物上,PEI-CDs 的 FL 信号被打开。该方法的检测限为 0.56μM,而线性响应范围为 5.56μM 至 277.8μM。

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