全自动开发和Box-Behnken优化的Eltrombopag Olamine的高级正相HPTLC分析

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Pranay M. Hadole, Saurabh B. Ganorkar, Suraj R. Chaudhari, Vaishali N. Sonawane, Preeti S. Bobade, Amod S. Patil, Atul A. Shirkhedkar
{"title":"全自动开发和Box-Behnken优化的Eltrombopag Olamine的高级正相HPTLC分析","authors":"Pranay M. Hadole,&nbsp;Saurabh B. Ganorkar,&nbsp;Suraj R. Chaudhari,&nbsp;Vaishali N. Sonawane,&nbsp;Preeti S. Bobade,&nbsp;Amod S. Patil,&nbsp;Atul A. Shirkhedkar","doi":"10.1007/s12247-024-09908-9","DOIUrl":null,"url":null,"abstract":"<div><h3>Purpose</h3><p>This study aimed to develop a normal-phase TLC densitometry/ high-performance thin-layer chromatography (HPTLC) protocol, assisted with an Automatic Development Chamber 2 (ADC 2) for the efficient and robust pharmaceutical quantification of a thrombopoietin receptor agonist Eltrombopag Olamine (ELTO) using experimental design.</p><h3>Methods</h3><p>The effect of various factors on HPTLC outcomes has been studied using the Box-Behnken Design (BBD) to enhance method robustness. The ADC 2 was employed as an advancement in the development of a validated normal-phase HPTLC protocol, improving the method’s reproducibility and accuracy.</p><h3>Results</h3><p>TLC densitometry scans were performed at 399 nm in reflectance mode optimizing the retention of ELTO at an R<sub><i>f</i></sub> value of 0.47 ± 0.02. The application of ADC 2 during the development minimized the impact of temperature and humidity. The BBD, supported with response surface methodology (RSM), was used to assess the method’s operable design region for increased robustness. The established linearity range was from 250 to 1500 ng per spot, with a regression coefficient (<i>r</i><sup>2</sup>) of 0.9998. The developed protocol was validated according to Q2(R2) recommendations of the International Council for Harmonization (ICH).</p><h3>Conclusion</h3><p>NP-HPTLC is unique, efficient, precise, reproducible, and robust for the rapid quantification of ELTO. The method also uses minimal amount of organic solvents compared to well-known techniques such as high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS). The protocol is timesaving, allowing the simultaneous analysis of multiple samples, making it an effective alternative for determining ELTO in pharmaceutical formulations.</p><h3>Graphical Abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":656,"journal":{"name":"Journal of Pharmaceutical Innovation","volume":"20 1","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Advanced Normal-Phase HPTLC Profiling of Eltrombopag Olamine with Automated Development and Box-Behnken Optimizations\",\"authors\":\"Pranay M. Hadole,&nbsp;Saurabh B. Ganorkar,&nbsp;Suraj R. Chaudhari,&nbsp;Vaishali N. Sonawane,&nbsp;Preeti S. Bobade,&nbsp;Amod S. Patil,&nbsp;Atul A. Shirkhedkar\",\"doi\":\"10.1007/s12247-024-09908-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Purpose</h3><p>This study aimed to develop a normal-phase TLC densitometry/ high-performance thin-layer chromatography (HPTLC) protocol, assisted with an Automatic Development Chamber 2 (ADC 2) for the efficient and robust pharmaceutical quantification of a thrombopoietin receptor agonist Eltrombopag Olamine (ELTO) using experimental design.</p><h3>Methods</h3><p>The effect of various factors on HPTLC outcomes has been studied using the Box-Behnken Design (BBD) to enhance method robustness. The ADC 2 was employed as an advancement in the development of a validated normal-phase HPTLC protocol, improving the method’s reproducibility and accuracy.</p><h3>Results</h3><p>TLC densitometry scans were performed at 399 nm in reflectance mode optimizing the retention of ELTO at an R<sub><i>f</i></sub> value of 0.47 ± 0.02. The application of ADC 2 during the development minimized the impact of temperature and humidity. The BBD, supported with response surface methodology (RSM), was used to assess the method’s operable design region for increased robustness. The established linearity range was from 250 to 1500 ng per spot, with a regression coefficient (<i>r</i><sup>2</sup>) of 0.9998. The developed protocol was validated according to Q2(R2) recommendations of the International Council for Harmonization (ICH).</p><h3>Conclusion</h3><p>NP-HPTLC is unique, efficient, precise, reproducible, and robust for the rapid quantification of ELTO. The method also uses minimal amount of organic solvents compared to well-known techniques such as high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS). The protocol is timesaving, allowing the simultaneous analysis of multiple samples, making it an effective alternative for determining ELTO in pharmaceutical formulations.</p><h3>Graphical Abstract</h3>\\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":656,\"journal\":{\"name\":\"Journal of Pharmaceutical Innovation\",\"volume\":\"20 1\",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-01-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pharmaceutical Innovation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s12247-024-09908-9\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmaceutical Innovation","FirstCategoryId":"3","ListUrlMain":"https://link.springer.com/article/10.1007/s12247-024-09908-9","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

本研究旨在建立一种正相薄层色谱/高效薄层色谱(HPTLC)方法,在自动开发室2 (ADC 2)的辅助下,对血小板生成素受体激动剂Eltrombopag Olamine (ELTO)进行高效、稳健的药物定量分析。方法采用Box-Behnken设计(BBD)研究各因素对HPTLC结果的影响,以提高方法的稳健性。ADC 2被用于开发一种有效的正相HPTLC协议,提高了方法的重复性和准确性。结果在399nm反射模式下进行密度扫描,使ELTO的保留率在0.47±0.02的范围内。在开发过程中,ADC 2的应用最大限度地减少了温度和湿度的影响。在响应面法(RSM)的支持下,BBD用于评估方法的可操作设计区域,以提高鲁棒性。建立的线性范围为250 ~ 1500 ng /点,回归系数(r2)为0.9998。制定的方案根据国际协调理事会(ICH) Q2(R2)建议进行验证。结论np - hptlc法可用于ELTO的快速定量分析,简便、准确、重复性好。与高效液相色谱(HPLC)和液相色谱-质谱(LC-MS)等知名技术相比,该方法还使用了最少的有机溶剂。该方案节省了时间,允许同时分析多个样品,使其成为测定药物制剂中ELTO的有效替代方案。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Advanced Normal-Phase HPTLC Profiling of Eltrombopag Olamine with Automated Development and Box-Behnken Optimizations

Advanced Normal-Phase HPTLC Profiling of Eltrombopag Olamine with Automated Development and Box-Behnken Optimizations

Purpose

This study aimed to develop a normal-phase TLC densitometry/ high-performance thin-layer chromatography (HPTLC) protocol, assisted with an Automatic Development Chamber 2 (ADC 2) for the efficient and robust pharmaceutical quantification of a thrombopoietin receptor agonist Eltrombopag Olamine (ELTO) using experimental design.

Methods

The effect of various factors on HPTLC outcomes has been studied using the Box-Behnken Design (BBD) to enhance method robustness. The ADC 2 was employed as an advancement in the development of a validated normal-phase HPTLC protocol, improving the method’s reproducibility and accuracy.

Results

TLC densitometry scans were performed at 399 nm in reflectance mode optimizing the retention of ELTO at an Rf value of 0.47 ± 0.02. The application of ADC 2 during the development minimized the impact of temperature and humidity. The BBD, supported with response surface methodology (RSM), was used to assess the method’s operable design region for increased robustness. The established linearity range was from 250 to 1500 ng per spot, with a regression coefficient (r2) of 0.9998. The developed protocol was validated according to Q2(R2) recommendations of the International Council for Harmonization (ICH).

Conclusion

NP-HPTLC is unique, efficient, precise, reproducible, and robust for the rapid quantification of ELTO. The method also uses minimal amount of organic solvents compared to well-known techniques such as high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS). The protocol is timesaving, allowing the simultaneous analysis of multiple samples, making it an effective alternative for determining ELTO in pharmaceutical formulations.

Graphical Abstract

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Pharmaceutical Innovation
Journal of Pharmaceutical Innovation PHARMACOLOGY & PHARMACY-
CiteScore
3.70
自引率
3.80%
发文量
90
审稿时长
>12 weeks
期刊介绍: The Journal of Pharmaceutical Innovation (JPI), is an international, multidisciplinary peer-reviewed scientific journal dedicated to publishing high quality papers emphasizing innovative research and applied technologies within the pharmaceutical and biotechnology industries. JPI''s goal is to be the premier communication vehicle for the critical body of knowledge that is needed for scientific evolution and technical innovation, from R&D to market. Topics will fall under the following categories: Materials science, Product design, Process design, optimization, automation and control, Facilities; Information management, Regulatory policy and strategy, Supply chain developments , Education and professional development, Journal of Pharmaceutical Innovation publishes four issues a year.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信