用于分离和鉴定倍他洛尔杂质和降解产物的 LC 和 LC-MS/MS 研究。

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Anis Chmangui, Mehdi Safta, Mohamed Ridha Driss, Soufiane Touil, Sondes Bouabdallah
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引用次数: 0

摘要

倍他洛尔(Bx)是一种选择性β1受体阻断剂,用于治疗高血压和青光眼。本研究旨在展示一种利用液相色谱法(LC)和液相色谱-电喷雾质谱法(LC-ESI/MS)同时分离、鉴定和表征倍他洛尔杂质和降解产物的方法,而无需从反应混合物中分离出这些杂质和降解产物。根据 ICH 指南,在最佳条件下,Bx 的检出限(LOD)和定量限(LOQ)分别为 5.46 和 16.54 μg mL-1。而主要降解产物 P6 的检出限和定量限分别为 2.15 和 6.53 μg mL-1。根据国际协调会议(ICH)指南 Q1A (R2),对倍他洛尔进行了水解(酸性和碱性)和氧化应激条件试验,结果发现该药物在酸性、碱性和氧化应激条件下均不稳定。根据 LC-ESI/MS 分析,结果显示 Bx 在酸性、碱性和氧化环境中均会分解。所有降解产物都是通过碎片模式和质谱分析得到的质量来确定的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LC and LC-MS/MS Studies for the Separation and Identification of Impurities and Degradation Products of Betaxolol.

Betaxolol (Bx) is a selective β1 receptor blocker used in the treatment of hypertension and glaucoma. The aim of the present work was to demonstrate an approach involving use of liquid chromatography (LC) and liquid chromatography-electrospray ionization mass spectrometry (LC-ESI/MS) for the simultaneous separation, identification and characterization of impurities and of degradation products of betaxolol without their isolation from the reaction mixtures. At optimum condition, and according to ICH guidelines, the limit of detection (LOD) and limit of quantification (LOQ) for Bx are found to be 5.46 and 16.54 μg mL-1, respectively. However, the LOD and LOQ for the major degradation product P6 were 2.15 and 6.53 μg mL-1. Betaxolol was subjected to hydrolytic (acidic and basic) and oxidative, stress conditions according to International Conference on Harmonization (ICH) guideline Q1A (R2), and as results, the drug was found to be labile in acidic, basic and oxidative stress conditions. Based on LC-ESI/MS analysis, the found results revealed that Bx decomposes in acidic, basic and oxidizing environments. All degradation products were identified with the help of their fragmentation pattern and the masses obtained upon the MS analysis.

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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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