Suppr超能文献

基于氨基酸的氮掺杂碳点的固相热解合成作为用于检测铜离子和谷胱甘肽的“关-开-关”荧光探针

Solid-Phase Pyrolysis Synthesis of Amino Acid-Based Nitrogen-Doped Carbon Dots as an "On-Off-On" Fluorescent Probe for the Detection of Copper Ions and Glutathione.

作者信息

Yao Zhuoru, Wang Cunjin, Ma Zixin, Huang Ruixin, Wang Baozhong, Zhang Jing, Zhao Xiaoliang, Zhang Weijie, Shi Huanxian

机构信息

School of Health Engineering, Lanzhou University of Information Science and Technology, Lanzhou, 730050, PR China.

School of Life Science and Engineering, Lanzhou University of Technology, Lanzhou, 730050, PR China.

出版信息

J Fluoresc. 2025 Feb 22. doi: 10.1007/s10895-025-04206-0.

Abstract

This study introduces the synthesis of amino acid-based nitrogen-doped carbon dots (N-L-Ser-CDs) from L-serine (L-Ser) and urea through a straightforward and economical one-step solid-phase pyrolysis process. The incorporation of nitrogen into the carbon dots resulted in a remarkable 27.6-fold increase in fluorescence intensity, featuring a peak emission at 405 nm when excited at 330 nm and a significant fluorescence quantum yield of 22.5%. These N-L-Ser-CDs displayed a specific binding affinity for Cu, leading to a pronounced fluorescence quenching effect. However, upon interaction with glutathione (GSH), the fluorescence of the N-L-Ser-CDs + Cu complex was selectively restored. This restoration was attributed to the displacement of Cu from the surface of the N-L-Ser-CDs due to the strong interaction between GSH and Cu. The mechanism underlying this fluorescence quenching was elucidated as an electron transfer process from the excited state of the N-L-Ser-CDs to Cu. Additionally, the sensor developed in this study exhibited a linear detection range of 0-90 µM for Cu with a detection limit of 3 µM, and a linear detection range of 0-120 µM with a detection limit of 3 µM for GSH. By integrating the detection capabilities for both Cu and GSH, a successful "on-off-on" fluorescent probe was developed. Most importantly, this proposed method offers simplicity, affordability, and ease of use, while also showing potential for practical GSH detection in real urine samples.

摘要

本研究介绍了通过简单且经济的一步固相热解过程,由L-丝氨酸(L-Ser)和尿素合成基于氨基酸的氮掺杂碳点(N-L-Ser-CDs)。氮掺入碳点导致荧光强度显著增加了27.6倍,在330 nm激发时,其发射峰位于405 nm,荧光量子产率高达22.5%。这些N-L-Ser-CDs对铜具有特异性结合亲和力,导致明显的荧光猝灭效应。然而,当与谷胱甘肽(GSH)相互作用时,N-L-Ser-CDs+Cu复合物的荧光被选择性恢复。这种恢复归因于GSH与铜之间的强相互作用,使得铜从N-L-Ser-CDs表面被取代。这种荧光猝灭的机制被阐明为从N-L-Ser-CDs的激发态到铜的电子转移过程。此外,本研究开发的传感器对铜的线性检测范围为0-90 μM,检测限为3 μM,对GSH的线性检测范围为0-120 μM,检测限为3 μM。通过整合对铜和GSH的检测能力,成功开发了一种“开-关-开”荧光探针。最重要的是,该方法具有简单、经济且易于使用的特点,同时在实际尿液样本中检测GSH方面也显示出潜力。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验