Smartphone-assisted fluorescence/colorimetric dual-mode sensing strategy for uranium ion detection using cerium-sulfonyl calix[4]arene

IF 5.3 2区 化学 Q1 CHEMISTRY, ANALYTICAL Microchimica Acta Pub Date : 2025-02-13 DOI:10.1007/s00604-025-07023-1
Lihao Xiong, Yuqi Tong, Jiayi Song, Sihan Chen, Yu Liu, Jinquan Liu, Le Li, Deshuai Zhen
{"title":"Smartphone-assisted fluorescence/colorimetric dual-mode sensing strategy for uranium ion detection using cerium-sulfonyl calix[4]arene","authors":"Lihao Xiong,&nbsp;Yuqi Tong,&nbsp;Jiayi Song,&nbsp;Sihan Chen,&nbsp;Yu Liu,&nbsp;Jinquan Liu,&nbsp;Le Li,&nbsp;Deshuai Zhen","doi":"10.1007/s00604-025-07023-1","DOIUrl":null,"url":null,"abstract":"<div><p> A novel fluorescence/colorimetric dual-mode detection strategy for uranium ions (UO<sub>2</sub><sup>2+</sup>) is presented based on a cerium-sulfonyl calix[4]arene (SC4A) platform. The exo- and endo-rim sites of SC4A can coordinate with Ce<sup>3+</sup> and Ce<sup>4+</sup> ions, respectively, quenching Ce<sup>3+</sup> fluorescence and influencing the oxidase-like activity of Ce<sup>4+</sup>. In the absence of UO<sub>2</sub><sup>2+</sup>, the solution of 3,3,5,5-tetramethylbenzidine (TMB) remains blue, but upon UO<sub>2</sub><sup>2+</sup> binding, Ce<sup>3+</sup> dissociates from SC4A, restoring fluorescence, while UO<sub>2</sub><sup>2+</sup> interacts with oxTMB, turning the solution from blue to colorless. This dual-mode system provides a linear fluorescence detection range of 30–800 nM with a detection limit of 20.20 nM, and a colorimetric range of 30–800 nM with a detection limit of 27.78 nM. By combining high-sensitivity fluorescence with visual colorimetric analysis, the proposed method possesses high sensitivity, accuracy, and reliability. Notably, smartphone-based color capture facilitates rapid and convenient sample analysis, enabling straightforward quantification at varying UO<sub>2</sub><sup>2+</sup> concentrations. The method has been successfully applied to real water and urine samples, demonstrating its practical utility in environmental and biological monitoring of UO<sub>2</sub><sup>2+</sup>.</p><h3>Graphical abstract</h3><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":705,"journal":{"name":"Microchimica Acta","volume":"192 3","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microchimica Acta","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s00604-025-07023-1","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

A novel fluorescence/colorimetric dual-mode detection strategy for uranium ions (UO22+) is presented based on a cerium-sulfonyl calix[4]arene (SC4A) platform. The exo- and endo-rim sites of SC4A can coordinate with Ce3+ and Ce4+ ions, respectively, quenching Ce3+ fluorescence and influencing the oxidase-like activity of Ce4+. In the absence of UO22+, the solution of 3,3,5,5-tetramethylbenzidine (TMB) remains blue, but upon UO22+ binding, Ce3+ dissociates from SC4A, restoring fluorescence, while UO22+ interacts with oxTMB, turning the solution from blue to colorless. This dual-mode system provides a linear fluorescence detection range of 30–800 nM with a detection limit of 20.20 nM, and a colorimetric range of 30–800 nM with a detection limit of 27.78 nM. By combining high-sensitivity fluorescence with visual colorimetric analysis, the proposed method possesses high sensitivity, accuracy, and reliability. Notably, smartphone-based color capture facilitates rapid and convenient sample analysis, enabling straightforward quantification at varying UO22+ concentrations. The method has been successfully applied to real water and urine samples, demonstrating its practical utility in environmental and biological monitoring of UO22+.

Graphical abstract

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
智能手机辅助荧光/比色双模式感应策略用于铈-磺酰基杯[4]芳烃铀离子检测
提出了一种基于铈磺酰基杯[4]芳烃(SC4A)平台的新型荧光/比色双模检测铀离子(UO22+)的策略。SC4A的外外和内边缘位点可以分别与Ce3+和Ce4+离子配位,猝灭Ce3+荧光,影响Ce4+的类氧化酶活性。在没有UO22+的情况下,3,3,5,5-四甲基联苯胺(TMB)的溶液保持蓝色,但UO22+结合后,Ce3+与SC4A解离,恢复荧光,而UO22+与oxTMB相互作用,使溶液由蓝色变为无色。该双模系统的线性荧光检测范围为30-800 nM,检出限为20.20 nM;比色范围为30-800 nM,检出限为27.78 nM。该方法将高灵敏度荧光分析与视觉比色分析相结合,具有较高的灵敏度、准确性和可靠性。值得注意的是,基于智能手机的颜色捕获有助于快速方便的样品分析,可以在不同的UO22+浓度下进行直接定量。该方法已成功应用于实际水和尿液样品中,证明了其在UO22+环境和生物监测中的实用性。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
文献相关原料
公司名称
产品信息
阿拉丁
sodium chloride (NaCl)
阿拉丁
acetic acid (HAc)
阿拉丁
3,3,5,5-Tetramethylbenzidine
阿拉丁
CeCl3
阿拉丁
4-sulfocalix[4]arene hydrate
来源期刊
Microchimica Acta
Microchimica Acta 化学-分析化学
CiteScore
9.80
自引率
5.30%
发文量
410
审稿时长
2.7 months
期刊介绍: As a peer-reviewed journal for analytical sciences and technologies on the micro- and nanoscale, Microchimica Acta has established itself as a premier forum for truly novel approaches in chemical and biochemical analysis. Coverage includes methods and devices that provide expedient solutions to the most contemporary demands in this area. Examples are point-of-care technologies, wearable (bio)sensors, in-vivo-monitoring, micro/nanomotors and materials based on synthetic biology as well as biomedical imaging and targeting.
期刊最新文献
A rime-like Au-Pt nanostructured film and polyaniline-MIP based electrochemical sensor for olanzapine detection. Ultra-sensitive glyphosate detection in soil and wastewater using Zn-zeolitic imidazolate framework-67/montmorillonite nanocomposite electrochemical sensor. Biosensing technologies for foodborne pathogen detection and healthcare: principles, emerging materials, and intelligent platforms. Locked nucleic acid probes enable enzyme-free photoelectrochemical detection of double-stranded DNA cancer biomarkers. Correction to: Simultaneous on-site screening of four prohibited anti-inflammatory drugs in herbal tea by a multiplex lateral flow immunoassay.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1