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高荧光碳点通过电子转移过程选择性可视化检测活细胞中的铜离子。

Highly fluorescent carbon dots as selective and visual probes for sensing copper ions in living cells via an electron transfer process.

机构信息

Key Laboratory on Luminescence and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, China.

Key Laboratory on Luminescence and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, China.

出版信息

Biosens Bioelectron. 2017 Nov 15;97:157-163. doi: 10.1016/j.bios.2017.05.035. Epub 2017 May 19.

DOI:10.1016/j.bios.2017.05.035
PMID:28595076
Abstract

As an integral part of many important enzymes, Cu is involved in a number of vital biological processes, which is linked to the oxidative damage and environmental contamination when Cu is excessive. In this work, Cu can be captured by the amino groups of carbon dots (CDs) to form complexes, resulting in a strong fluorescence quenching of CDs via a nonradiative electron transfer process, which offered a rapid, visual, and selective methodology for Cu detection. The probe exhibited a wide response concentration range (0.01-2μM) to Cu with a detection limit of 6.7nM. Significantly, the CDs presented excellent biocompatibility and high photostability, which were applicable for the visualization of Cu dynamic invasion into living cells and Tilapia mossambica. Furthermore, the toxicity of Cu ions to living cells could be inhibited with CDs by the formation of complexes.

摘要

作为许多重要酶的组成部分,铜参与了许多重要的生物过程,而当铜过量时,会与氧化损伤和环境污染有关。在这项工作中,铜可以被碳点(CDs)的氨基捕获形成配合物,通过非辐射电子转移过程导致 CDs 的荧光猝灭,为铜的检测提供了一种快速、直观、选择性的方法。该探针对铜的响应浓度范围很宽(0.01-2μM),检测限为 6.7nM。值得注意的是,CDs 具有良好的生物相容性和高的光稳定性,适用于可视化铜动态入侵活细胞和罗非鱼。此外,通过形成配合物,CDs 可以抑制铜离子对活细胞的毒性。

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