Selective fluorescence detection of acetylsalicylic acid, succinic acid and ascorbic acid based on a responsive lanthanide metal fluorescent coordination polymer†

IF 2.7 3区 化学 Q2 CHEMISTRY, ANALYTICAL Analytical Methods Pub Date : 2024-06-25 DOI:10.1039/D4AY00696H
Guo-Ying Chen, Mao-Ling Luo, Li Chen, Jia-Li Wang, Tong-Qing Chai, Dan Wang and Feng-Qing Yang
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Abstract

A fluorescent sensor for highly selective and ultrasensitive detection of acetylsalicylic acid (ASA), succinic acid (SA), and ascorbic acid (AA) was reported. The water-soluble fluorescent ligand salicylic acid (Sal) was generated through catalyzing ASA by the hydrolase activity of zeolitic-imidazolate framework-8 (ZIF-8) or natural esterase (Est). The Sal can coordinate with 2-methylimidazole (2-MIm) and Ln(III) to form a fluorescent lanthanide coordination polymer (LCP), which has a fluorescence emission peak with the maximum wavelength at 412 nm (the excitation wavelength at 300 nm). Therefore, the detection of ASA can be achieved through the fluorescence intensity changes of LCPs in the system, which has comparable sensitivity and good selectivity (linear range of 0.031–1.00 mM and LODs of 11.72 and 3.22 μM) as compared to a direct reaction between Est/ZIF-8 and ASA for detecting ASA (linear range of 0.05–1.20 mM and limits of detection (LODs) of 4.43 and 4.58 μM). Furthermore, upon the addition of SA and AA, the fluorescence intensity of the reaction system can be enhanced and weakened through changing the energy resonance transfer pathways and affecting the enzymatic reaction process, respectively, realizing their sensitive and selective fluorescence detection. The established fluorescent sensors can work well in a wide linear range of SA concentrations from 0 to 2.50 mM (Est-based reaction system) and 0 to 1.50 mM (ZIF-8-based reaction system) with the LODs of 0.032 and 0.028 mM, respectively. The linear ranges of AA concentrations are from 0.0078 to 0.25 mM (Est-based reaction system) and 0.0078 to 0.13 mM (ZIF-8-based reaction system) with the LODs of 2.54 and 3.80 μM, respectively. The established sensors were successfully used in the detection of SA in rabbit plasma, with a recovery of 84.0%–98.7%. Additionally, the contents of ASA in Aspirin Enteric-Coated tablets and AA in vitamin C tablets were also determined by the developed methods.

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基于响应性镧系金属荧光配位聚合物的乙酰水杨酸、琥珀酸和抗坏血酸选择性荧光检测技术
报告了一种用于高选择性和超灵敏度检测乙酰水杨酸(ASA)、琥珀酸(SA)和抗坏血酸(AA)的荧光传感器。水溶性荧光配体水杨酸(Sal)是通过沸石咪唑框架-8(ZIF-8)或天然酯酶(Est)的水解酶活性催化 ASA 生成的。Sal 能与 2-甲基咪唑(2-MIm)和 Ln(III)配位形成荧光镧系配位聚合物(LCPs),其荧光发射峰的最大波长为 412 nm(激发波长为 300 nm)。因此,可以通过系统中 LCPs 的荧光强度变化来检测 ASA,与 Est/ZIF-8 与 ASA 直接反应检测 ASA 相比(线性范围为 0.05-1.20 mM,检测限为 4.43 和 4.58 μM),灵敏度相当,选择性好(线性范围为 0.031-1.00 mM,检测限为 11.72 和 3.22 μM)。此外,加入 SA 和 AA 后,反应体系的荧光强度可分别通过改变能量共振传递途径和影响酶促反应过程而增强和减弱,从而实现其灵敏度和选择性荧光检测。所建立的荧光传感器可在 0 至 2.50 mM(基于 Est 的反应体系)和 0 至 1.50 mM(基于 ZIF-8 的反应体系)的宽线性范围内良好工作,LOD 分别为 0.032 和 0.028 mM。AA 浓度的线性范围分别为 0.0078 至 0.25 mM(基于 Est 的反应体系)和 0.0078 至 0.13 mM(基于 ZIF-8 的反应体系),检测限分别为 2.54 和 3.80 μM。所建立的传感器成功用于兔血浆中 SA 的检测,回收率为 84.0%-98.7% 。此外,所建立的方法还测定了阿司匹林肠溶片中的ASA含量和维生素C片中的AA含量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
期刊最新文献
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