中央配合物设计专家支持的RP-HPLC法优化和定量评价盐酸埃夫尼地平片中乙醇和氯噻酮的含量。

IF 1.3 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS Journal of chromatographic science Pub Date : 2024-07-10 DOI:10.1093/chromsci/bmad077
Bhoomi D Patel, Hitesh J Vekaria
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引用次数: 0

摘要

基于中心复合设计的RP-HPLC法优化盐酸乙磺酸埃夫尼地平(EFE)和氯噻酮(CHL)片剂的同步分析。使用Inertsil ODS C18柱(250 × 4.6mm,5μm),PDA检测器,具有0.05M KH2PO4缓冲液(pH 4.5):乙腈(40:60%v/v)流动相。研究的自变量包括KH2PO4的浓度(X1)和流动相的流速(X2)。根据获得的响应(保留时间、分辨率和拖尾因子),选择的最佳条件为X1 = 40%和X2 = 1毫升/分钟。通过评估验证参数对优化的HPLC条件进行了验证,并符合ICH设定的验收标准。线性校准曲线在6.25-18.75和20-60μg/ml范围内。CHL和EFE的药物含量分别为100.94%和100.06%。经验证的RP-HPLC-PDA方法可用于片剂中EFE和CHL的常规分析。
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Central Composite Design Expert-Supported RP-HPLC Optimization and Quantitative Evaluation of Efonidipine Hydrochloride Ethanolate & Chlorthalidone in Tablet.

Central composite design based RP-HPLC method optimization for the synchronized analysis of Efonidipine Hydrochloride Ethanolate (EFE) and Chlorthalidone (CHL) in tablet. The effective separation was performed using Inertsil ODS C18 column (250 × 4.6 mm, 5 μm), PDA detector with 0.05 M KH2PO4 Buffer (pH 4.5): Acetonitrile (40:60%v/v) mobile phase. Independent variables were investigated include the concentration of KH2PO4 (X1) and flow rate of mobile phase (X2). Based on responses obtained (retention time, resolution and tailing factor), the optimum condition selected was X1 = 40% and X2 = 1 ml/min. Optimized HPLC condition was validated by assessing validation parameters and it meets the acceptance criteria set by ICH. The linear calibration curve was found to be in the quantity range 6.25-18.75 and 20-60 μg/ml Assay of drugs was 100.94 and 100.06% for CHL and EFE. The validated RP-HPLC-PDA method can be used for routine analysis of EFE and CHL in tablet.

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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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