Sharib Raza Khan, Shailesh Dadge, Shivam Rathaur, Jiaur R. Gayen
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The Picroside II separation was successfully done on the HPLC system of Waters equipped through UV-Visible detector on Waters X Bridge RP C18 column having dimensions (4.6 mm × 150 mm, 5.0 μm), mobile phase containing 0.1% formic acid and acetonitrile (77:23%v/v), and rate of flow at 1.0 mL/min. The wavelength for detection was 266 nm; retention time of Picroside II was between 6.0 and 6.2 min with a total duration run time of 10 min. The proposed developed technique was found to be specific, precise (% RSD < 2%), linear (6–14 μg/mL), and robust (% RSD < 1%). Additionally, forced degradation studies were established and the % drug assay was found to be 99.46 ± 0.86% including the results of specificity in terms of peak purity suggesting no interference of any unidentified peak with the chromatographic peak of Picroside II. The results of all the method validation parameters were within the recommended limit of ICH Q2(R1) guidelines. The proposed method was proved to be green as performed by green assessment tools.</p><h3>Conclusion</h3><p>The AQbD-based developed method helped in the design and operating space generating with the knowledge of all the method validation characteristics, and the developed RP-HPLC method on the AQbD-based approach was very useful for Picroside II estimation in bulk and pharmaceutical dosage forms.</p></div>","PeriodicalId":577,"journal":{"name":"Future Journal of Pharmaceutical Sciences","volume":"11 1","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://fjps.springeropen.com/counter/pdf/10.1186/s43094-025-00885-5","citationCount":"0","resultStr":"{\"title\":\"Analytical quality by design (AQbD) assisted RP-HPLC technique for quantification of Picroside II in bulk and pharmaceutical dosage form\",\"authors\":\"Sharib Raza Khan, Shailesh Dadge, Shivam Rathaur, Jiaur R. Gayen\",\"doi\":\"10.1186/s43094-025-00885-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Quality by design (QbD) adverts toward gaining of few expected quality with predetermined and desired specifications. Analytical quality by design (AQbD) approach toward the development of analytical method can significantly lead toward the rugged and robust method specially the assessment and risk management compared to traditional approaches. The aim of present study is to develop an analytical method for the estimation of Picroside II in bulk and pharmaceutical dosage form through RP-HPLC assisted by AQbD.</p><h3>Result</h3><p>The important critical parameters were methodically optimized by the experimental design space of Box–Behnken, and model graphs were plotted by utilizing Design Expert Software trial version 13.0. 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引用次数: 0
摘要
设计质量(QbD)旨在通过预先确定的和期望的规格获得少数期望的质量。分析方法的发展与传统方法相比,采用设计分析质量(AQbD)方法可以显著地导致分析方法特别是评估和风险管理方法的坚固和稳健。本研究的目的是建立一种用AQbD辅助RP-HPLC法测定原料药和制剂中picro甙II含量的分析方法。结果采用Box-Behnken实验设计空间对重要关键参数进行了系统优化,并利用design Expert Software试用版13.0绘制了模型图。采用Waters X Bridge RP C18色谱柱(尺寸为4.6 mm × 150 mm, 5.0 μm)紫外可见检测器,流动相为0.1%甲酸和乙腈(77%:23%v/v),流速为1.0 mL/min,在Waters公司的高效液相色谱系统上成功分离了Picroside II。检测波长为266 nm;Picroside II的停留时间为6.0 ~ 6.2 min,总停留时间为10 min。结果表明,该方法具有特异性、精密度(% RSD < 2%)、线性(6 ~ 14 μg/mL)和鲁棒性(% RSD < 1%)。此外,建立了强制降解研究,发现药物含量测定为99.46±0.86%,包括峰纯度的特异性结果,表明任何未识别的峰与Picroside II的色谱峰没有干扰。所有方法验证参数的结果均在ICH Q2(R1)指南的推荐范围内。通过绿色评估工具验证了该方法的绿色性。结论基于aqbd建立的方法在了解所有方法验证特性的基础上,有助于设计和操作空间的生成,在aqbd基础上建立的RP-HPLC方法可用于原料药和制剂中picro甙II的估计。
Analytical quality by design (AQbD) assisted RP-HPLC technique for quantification of Picroside II in bulk and pharmaceutical dosage form
Background
Quality by design (QbD) adverts toward gaining of few expected quality with predetermined and desired specifications. Analytical quality by design (AQbD) approach toward the development of analytical method can significantly lead toward the rugged and robust method specially the assessment and risk management compared to traditional approaches. The aim of present study is to develop an analytical method for the estimation of Picroside II in bulk and pharmaceutical dosage form through RP-HPLC assisted by AQbD.
Result
The important critical parameters were methodically optimized by the experimental design space of Box–Behnken, and model graphs were plotted by utilizing Design Expert Software trial version 13.0. The Picroside II separation was successfully done on the HPLC system of Waters equipped through UV-Visible detector on Waters X Bridge RP C18 column having dimensions (4.6 mm × 150 mm, 5.0 μm), mobile phase containing 0.1% formic acid and acetonitrile (77:23%v/v), and rate of flow at 1.0 mL/min. The wavelength for detection was 266 nm; retention time of Picroside II was between 6.0 and 6.2 min with a total duration run time of 10 min. The proposed developed technique was found to be specific, precise (% RSD < 2%), linear (6–14 μg/mL), and robust (% RSD < 1%). Additionally, forced degradation studies were established and the % drug assay was found to be 99.46 ± 0.86% including the results of specificity in terms of peak purity suggesting no interference of any unidentified peak with the chromatographic peak of Picroside II. The results of all the method validation parameters were within the recommended limit of ICH Q2(R1) guidelines. The proposed method was proved to be green as performed by green assessment tools.
Conclusion
The AQbD-based developed method helped in the design and operating space generating with the knowledge of all the method validation characteristics, and the developed RP-HPLC method on the AQbD-based approach was very useful for Picroside II estimation in bulk and pharmaceutical dosage forms.
期刊介绍:
Future Journal of Pharmaceutical Sciences (FJPS) is the official journal of the Future University in Egypt. It is a peer-reviewed, open access journal which publishes original research articles, review articles and case studies on all aspects of pharmaceutical sciences and technologies, pharmacy practice and related clinical aspects, and pharmacy education. The journal publishes articles covering developments in drug absorption and metabolism, pharmacokinetics and dynamics, drug delivery systems, drug targeting and nano-technology. It also covers development of new systems, methods and techniques in pharmacy education and practice. The scope of the journal also extends to cover advancements in toxicology, cell and molecular biology, biomedical research, clinical and pharmaceutical microbiology, pharmaceutical biotechnology, medicinal chemistry, phytochemistry and nutraceuticals.