碳点用于检测雷尼替丁并阐明检测机制

IF 2.6 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Mei Zhang, Jingwen Zhao, Yingying Long, Changsong Li, Xiaoming Yang
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引用次数: 0

摘要

碳点(CD)因其优越的光学性能和令人满意的稳定性,已被广泛应用于多个领域,尤其是在药物分析领域。本文以乙二胺四乙酸二钠和磷酸为原料,通过简便的微波法快速合成了一种可溶性亮蓝荧光碳点。重要的是,在这些光盘中引入雷尼替丁会导致其荧光减弱,从而成功建立了一种创新的检测雷尼替丁的方法,该方法具有良好的选择性和抗干扰能力。在最佳条件下,F0/F与雷尼替丁浓度的标准曲线图在6-2000 µM范围内呈线性关系,相关系数为0.9833,检测限为4.2 µM。同时,我们还探讨了 CD 对雷尼替丁的检测机制,并将其阐述为内滤效应。因此,我们可以在 CD 的基础上拓宽检测雷尼替丁的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Carbon Dots Employed for the Detection of Ranitidine and Elaborating the Detecting Mechanism

Carbon Dots Employed for the Detection of Ranitidine and Elaborating the Detecting Mechanism

Carbon dots (CDs) has been widely utilized in multiple fields, especially towards kinds of drug analyses, owing to its superior optical properties and satisfactory stability. Herein, we rapidly synthesized one kind of soluble bright-blue fluorescent CDs through a facile microwave method, while disodium ethylenediaminetetraacetic acid and phosphoric acid served as the raw materials. Importantly, introducing ranitidine into these CDs resulted in its decreased fluorescence, and thus an innovative method of detecting ranitidine was successfully established, which showed the favorable selectivity and anti-interference ability. With the optimal conditions, the standard curve diagram of F0/F against concentration of ranitidine was linear in the range of 6-2000 µM with a correlation coefficient of 0.9833, and the limit of detection (LOD) was calculated to be 4.2 µM. Meanwhile, we also explored the detecting mechanism of ranitidine by CDs, and elaborated that as the internal filtration effect. Consequently, we may broaden the avenues of detecting ranitidine on the basis of CDs.

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来源期刊
Journal of Fluorescence
Journal of Fluorescence 化学-分析化学
CiteScore
4.60
自引率
7.40%
发文量
203
审稿时长
5.4 months
期刊介绍: Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.
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