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用于美沙拉嗪选择性传感的水相胶束溶液中呋喃开环反应的性质。

Properties of a furan ring-opening reaction in aqueous micellar solutions for selective sensing of mesalazine.

作者信息

Sabahi-Agabager Leila, Eskandari Habibollah, Nasiri Farough, Shamkhali Amir Nasser, Baghi Sefidan Somayyeh

机构信息

Department of Chemistry, Faculty of Basic Sciences, University of Mohaghegh Ardabili, Ardabil 56199-11367, Iran.

Department of Chemistry, Faculty of Basic Sciences, University of Mohaghegh Ardabili, Ardabil 56199-11367, Iran.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2021 Sep 5;258:119846. doi: 10.1016/j.saa.2021.119846. Epub 2021 Apr 17.

Abstract

A novel and efficient non-azo formation based method was developed for trace sensing of mesalazine (MES), a pharmaceutical aromatic amine. MES was simply coupled with a Meldrum's activated furan (MAF) reagent via a furan ring opening reaction to form a colored product. The intense purple colored solution was detected at 575 nm. The reaction of MES with MAF was monitored by employing H NMR spectroscopy and mass spectrometry. In addition, density functional theory (DFT) was applied to optimize the structure of the colored product and its λ (the wavelength of maximum absorbance) in dimethyl sulfoxide and water. The colored product was considered in three possible structures, and the most possible structures in dimethyl sulfoxide and in water were identified by employing the DFT calculations. Both of the most possible structures indicated only a local excitation in their λ and no charge transfer was observed. However, one of the structures in dimethyl sulfoxide presented charge transfer properties occurring through NCCC moiety. A univariate optimization method was also used to attain the optimum condition for analysis. In addition, the dependence of the analytical response on the three main affecting parameters (reaction time (X), Triton X-100 concentration (X) and MAF concentration (X)) was identified by employing a central composite design (CCD) approach. The CCD study showed that the analytical response depends complexly on the parameters. Beer's law was obeyed within the range of 0.06-9.30 μg mL of MES (155 fold linearity) at 575 nm, under the optimum condition introduced by the CCD approach. Also, the limit of detection was obtained 0.04 μg mL of MES. The method showed precision (as relative standard deviation) and accuracy (as recovery) within the ranges of 0.6-3.2 % and 96.3-100.8%, respectively. Various organic and inorganic species, amino-pharmaceuticals, and amino acids were tested to evaluate the selectivity of the method. The selectivity of the analytical method was satisfactory. The method was successfully applied for detection of MES in various water matrices and pharmaceutical tablets.

摘要

开发了一种新颖且高效的基于非偶氮形成的方法,用于痕量检测美沙拉嗪(MES),一种药物芳香胺。MES通过呋喃开环反应与丙二酸环亚异丙酯活化呋喃(MAF)试剂简单偶联,形成有色产物。在575nm处检测到强烈的紫色溶液。采用核磁共振氢谱(H NMR)光谱和质谱监测MES与MAF的反应。此外,应用密度泛函理论(DFT)优化有色产物在二甲基亚砜和水中的结构及其λ(最大吸收波长)。考虑了有色产物的三种可能结构,并通过DFT计算确定了在二甲基亚砜和水中最可能的结构。两种最可能的结构在其λ处仅显示局部激发,未观察到电荷转移。然而,二甲基亚砜中的一种结构通过NCCC部分呈现电荷转移性质。还采用单变量优化方法获得分析的最佳条件。此外,采用中心复合设计(CCD)方法确定了分析响应对三个主要影响参数(反应时间(X)、吐温X - 100浓度(X)和MAF浓度(X))的依赖性。CCD研究表明,分析响应复杂地依赖于这些参数。在CCD方法引入的最佳条件下,在575nm处,美沙拉嗪浓度在0.06 - 9.30μg mL范围内符合比尔定律(线性范围为155倍)。此外,美沙拉嗪检测限为0.04μg mL。该方法的精密度(以相对标准偏差计)和准确度(以回收率计)分别在0.6 - 3.2%和96.3 - 100.8%范围内。测试了各种有机和无机物种、氨基药物和氨基酸,以评估该方法的选择性。该分析方法的选择性令人满意。该方法成功应用于检测各种水基质和药物片剂中的美沙拉嗪。

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