Synergism of Photo-Induced Electron Transfer and Aggregation-Induced Quenching Mechanisms for Highly Sensitive Detection of Silver Ion and Captopril

Author:

Zhu Jing1,Hu Lei1,Meng Xiangying2ORCID,Li Feng1,Wang Wenjuan1,Shi Guiyang1,Wang Zhongxia1ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Yancheng Institute of Technology, Yancheng 224051, China

2. School of Medical Laboratory, Weifang Medical University, Weifang 261053, China

Abstract

Carbon-based nanoprobes, with excellent physicochemical performance and biocompatibility, are a kind of ideal nanomaterial for biosensing. Herein, we designed and prepared novel oxygen-doped nitrogen-enrichment carbon nanoribbons (ONCNs) with an excellent optical performance and uniform morphology, which could be used as a dual-mode fluorescence probe for the detection of Ag+ ion and captopril (Ctl) based on the synergism of photo-induced electron transfer and aggregation-induced quenching mechanisms. By recording the changes in fluorescent intensities of ONCNs, the Ag+ ion and Ctl concentrations can be easily tested in real samples. The results displayed that two good linear relationships existed between the change in fluorescent intensity of ONCNs and the concentrations of Ag+ ion and Ctl in the ranges of 3 μM to 30 μM and 1 μM to 30 μM, with the detection limit of 0.78 µM and 74 nM, respectively. The proposed sensing platform has also been successfully applied for the Ctl analysis in commercial tablet samples based on its high selectivity, proving its value in practical applications.

Funder

the National Natural Science Foundation of China

the Natural Science Foundation of Shandong Province

the Medicine and Health Science and Technology Development Plan Project of Shandong Province

the Funding for School-Level Research Projects of Yancheng Institute of Technology

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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