{"title":"鱼骨图平衡高效液相色谱法的五步方案:解开效率与可持续性的协同关系,在异烟肼、吡嗪酰胺和利福平固定剂量联合分析中的应用","authors":"Rana W. Gaber, Amr M. Mahmoud, Sarah S. Saleh","doi":"10.1002/jssc.70241","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>A five-step plan is presented to propose an HPLC method with the aid of the fishbone diagram to balance efficiency and sustainability. The five steps include method development, method optimization, method validation, greenness assessment, and sustainability profiling. A sensitive, accurate, robust, and rapid HPLC method has been developed for simultaneous determination and separation of anti-tubercular medications: rifampicin (RIF), isoniazid (INH), and pyrazinamide (PYR) in a fixed dose combination (FDC). The separation was attained by using a stationary phase Kromasil C<sub>18</sub> column (250 mm, 4.6,5 µm), accompanied by a gradient mode of the mobile phase in which the first solution was made up by using acetonitrile and phosphate buffer in a ratio of 4:96 v/v, and the second solution consisted of phosphate buffer and acetonitrile in ratio 45:55 v/v. The method was optimized by applying a fractional factorial design (2<sup>2</sup>), where the flow rate was set at 1.5 mL/min, the injection volume was 10 µL, and the detection was performed at 238 nm at a temperature of 35°C. The retention time for INH, PYR, and RIF were 3.82, 5.36, and 8.72 min (±0.02), respectively. The method was validated per the ICH guidelines, and the proposed method was found to be accurate, robust, precise, and selective. A design of experiment was established to assess the robustness of the study, where the obtained results proved that the developed method is robust. Two greenness tools, namely moGAPI and AGREE, were used to evaluate the method's greenness. In addition, the method was subjected to sustainability profiling using the EVG framework, where the suggested method was compared to other reported methods. The proposed method was found to be more sustainable and green, with a low negative impact on the environment.</p>\n </div>","PeriodicalId":17098,"journal":{"name":"Journal of separation science","volume":"48 8","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Five-Step Plan for Proposing a Balanced HPLC Method via Fishbone Diagram: Untangling the Synergy of Efficiency and Sustainability, Application on the Analysis of Isoniazid, Pyrazinamide, and Rifampicin in a Fixed Dose Combination\",\"authors\":\"Rana W. Gaber, Amr M. Mahmoud, Sarah S. 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The method was optimized by applying a fractional factorial design (2<sup>2</sup>), where the flow rate was set at 1.5 mL/min, the injection volume was 10 µL, and the detection was performed at 238 nm at a temperature of 35°C. The retention time for INH, PYR, and RIF were 3.82, 5.36, and 8.72 min (±0.02), respectively. The method was validated per the ICH guidelines, and the proposed method was found to be accurate, robust, precise, and selective. A design of experiment was established to assess the robustness of the study, where the obtained results proved that the developed method is robust. Two greenness tools, namely moGAPI and AGREE, were used to evaluate the method's greenness. In addition, the method was subjected to sustainability profiling using the EVG framework, where the suggested method was compared to other reported methods. 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引用次数: 0
摘要
提出了一种利用鱼骨图来平衡效率和可持续性的高效液相色谱方法的五步计划。这五个步骤包括方法开发、方法优化、方法验证、绿色评估和可持续性分析。建立了一种灵敏、准确、稳健、快速的高效液相色谱方法,用于同时测定和分离利福平(RIF)、异烟肼(INH)和吡嗪酰胺(PYR)等抗结核药物的固定剂量组合(FDC)。采用固定相Kromasil C18色谱柱(250 mm, 4.6,5µm)进行分离,采用流动相梯度模式,其中第一溶液由乙腈和磷酸缓冲液组成,比例为4:96 v/v,第二溶液由磷酸缓冲液和乙腈组成,比例为45:55 v/v。采用分数因子设计(22)对方法进行优化,流速为1.5 mL/min,进样量为10µL,检测波长为238 nm,温度为35℃。INH、PYR和RIF的保留时间分别为3.82、5.36和8.72 min(±0.02)。根据ICH指南对该方法进行了验证,发现该方法准确、稳健、精确和选择性强。建立了实验设计来评估研究的稳健性,得到的结果证明了所开发的方法是稳健性的。使用moGAPI和AGREE两种绿色度工具来评估方法的绿色度。此外,使用EVG框架对该方法进行了可持续性分析,并将建议的方法与其他报告的方法进行了比较。结果表明,该方法更具可持续性和绿色环保性,对环境的负面影响较小。
Five-Step Plan for Proposing a Balanced HPLC Method via Fishbone Diagram: Untangling the Synergy of Efficiency and Sustainability, Application on the Analysis of Isoniazid, Pyrazinamide, and Rifampicin in a Fixed Dose Combination
A five-step plan is presented to propose an HPLC method with the aid of the fishbone diagram to balance efficiency and sustainability. The five steps include method development, method optimization, method validation, greenness assessment, and sustainability profiling. A sensitive, accurate, robust, and rapid HPLC method has been developed for simultaneous determination and separation of anti-tubercular medications: rifampicin (RIF), isoniazid (INH), and pyrazinamide (PYR) in a fixed dose combination (FDC). The separation was attained by using a stationary phase Kromasil C18 column (250 mm, 4.6,5 µm), accompanied by a gradient mode of the mobile phase in which the first solution was made up by using acetonitrile and phosphate buffer in a ratio of 4:96 v/v, and the second solution consisted of phosphate buffer and acetonitrile in ratio 45:55 v/v. The method was optimized by applying a fractional factorial design (22), where the flow rate was set at 1.5 mL/min, the injection volume was 10 µL, and the detection was performed at 238 nm at a temperature of 35°C. The retention time for INH, PYR, and RIF were 3.82, 5.36, and 8.72 min (±0.02), respectively. The method was validated per the ICH guidelines, and the proposed method was found to be accurate, robust, precise, and selective. A design of experiment was established to assess the robustness of the study, where the obtained results proved that the developed method is robust. Two greenness tools, namely moGAPI and AGREE, were used to evaluate the method's greenness. In addition, the method was subjected to sustainability profiling using the EVG framework, where the suggested method was compared to other reported methods. The proposed method was found to be more sustainable and green, with a low negative impact on the environment.
期刊介绍:
The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.