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微波辅助简便合成的碳点作为生物样品中汞离子和碘离子的“开-关-开”荧光探针及用于细胞成像

Microwave-assisted Facile Synthesized Carbon Dots as "on-off-on" Fluorescence Probes for Mercury and Iodine Ions in Bio-samples and Cell Imaging.

作者信息

Gan Mingyu, Xu Yichen, Tan Jie, Wei Jieyin, Wang Ning, Wang Jianhua

机构信息

Department of Basic Medicine, Shanxi Medical University, Jinzhong, People's Republic of China.

Xiangya School of Medicine, Central South University, Changsha, People's Republic of China.

出版信息

J Fluoresc. 2024 Jul 25. doi: 10.1007/s10895-024-03821-7.

Abstract

A kind of nitrogen and sulfur co-doped CDs (N, S-CDs) was facilely synthesized using thiourea and citric acid as precursors, which established an "on-off-on" fluorescence probe to sequential detecting mercury and iodine ions inside water and biology samples. Under 360 nm excitation, CDs emit blue fluorescence with an optimal emission peak of 425 nm (on). The fluorescence of CDs experiences a significant quenching effect upon interaction with Hg ions due to the electron transfer between CDs and Hg. This quenching effect is subsequently recovered upon the addition of I owing to the formation of complexes between Hg and I. The probe exhibits high selectivity and sensitivity toward Hg and I with broad linearity in the range of 5-50 μM and 15-60 μM, respectively, and a low detection limit of 14.336 nM and 38.213 nM, respectively. The constructed fluorescence probe N, S-CDs has been successfully applied to the detection of Hg and I in water and biological samples with great recoveries. More importantly, the bioimaging study demonstrated that N, S-CDs are suitable for live monitoring in biological imaging scenarios of Hg and I in living cells.

摘要

一种氮硫共掺杂的碳点(N,S-CDs)通过使用硫脲和柠檬酸作为前驱体被简便地合成出来,该碳点构建了一种“关-开-关”荧光探针,用于顺序检测水和生物样品中的汞离子和碘离子。在360nm激发下,碳点发出蓝色荧光,最佳发射峰为425nm(开启状态)。由于碳点与汞之间的电子转移,碳点的荧光在与汞离子相互作用时会经历显著的猝灭效应。由于汞与碘形成络合物,在加入碘后这种猝灭效应随后恢复。该探针对汞和碘表现出高选择性和灵敏度,线性范围分别在5-50μM和15-60μM之间,检测限分别低至14.336nM和38.213nM。构建的荧光探针N,S-CDs已成功应用于水和生物样品中汞和碘的检测,回收率很高。更重要的是,生物成像研究表明N,S-CDs适用于在活细胞中汞和碘的生物成像场景下进行实时监测。

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