Issue 2, 2025

Selective fluorescent probe for Tl3+ ions through metal-induced hydrolysis and its application for direct assay of artificial urine

Abstract

In this research, we report a simple fluorescent probe designed to detect thallium(III) ions (Tl3+) in artificial urine samples. The Tl3+ signaling probe (TP-1) was readily prepared from 2-acetyl-6-methoxynaphthalene and hydrazine. In a pH 4.8 acetate buffer solution containing 1% (v/v) N,N-dimethylformamide as a solubilizer, probe TP-1 exhibited turn-on fluorescence signaling behavior in the presence of Tl3+. Other metal ions, anions, and major urine components such as uric acid, urea, and creatinine did not produce any noticeable fluorescence changes. The Tl3+ signaling of TP-1 was attributed to the hydrolysis of the hydrazone moiety, yielding the parent fluorophore 2-acetyl-6-methoxynaphthalene. The detection limit of TP-1 for Tl3+ sensing was 19 nM, and the signaling was completed within 2 min. Additionally, to further optimize the Tl3+ signaling of the hydrazone derivatives, we compared the effect of structural variations between the closely related ketone-hydrazone (TP-1) and aldehyde-hydrazone (TP-2) derivatives. We confirmed that the ketone-hydrazone (TP-1) demonstrated rapid and stable Tl3+ signaling behavior with satisfactory stability under the measurement conditions. Finally, as a practical application, a Tl3+ assay in artificial urine samples was performed using a smartphone as a portable signaling measurement and data analysis device.

Graphical abstract: Selective fluorescent probe for Tl3+ ions through metal-induced hydrolysis and its application for direct assay of artificial urine

Supplementary files

Article information

Article type
Paper
Submitted
18 Sep 2024
Accepted
19 Dec 2024
First published
15 Jan 2025
This article is Open Access
Creative Commons BY license

RSC Adv., 2025,15, 1336-1343

Selective fluorescent probe for Tl3+ ions through metal-induced hydrolysis and its application for direct assay of artificial urine

M. G. Choi, Y. Jang, M. G. Kim, S. Ahn and S. Chang, RSC Adv., 2025, 15, 1336 DOI: 10.1039/D4RA06726F

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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