绿色分析化学和设计质量:为癌症患者同时测定来曲唑和唑来膦酸的联合方法

Nourhan A. Abd El-Fatah , Heba T. Elbalkiny , Maha A. Hegazy , Manal Mohammed Fouad , Ghada M. El-Sayed
{"title":"绿色分析化学和设计质量:为癌症患者同时测定来曲唑和唑来膦酸的联合方法","authors":"Nourhan A. Abd El-Fatah ,&nbsp;Heba T. Elbalkiny ,&nbsp;Maha A. Hegazy ,&nbsp;Manal Mohammed Fouad ,&nbsp;Ghada M. El-Sayed","doi":"10.1016/j.jpbao.2024.100036","DOIUrl":null,"url":null,"abstract":"<div><p>Nowadays, breast cancer is the most affecting and globally diagnosed malignancy among women, yet Letrozole (LTZ) was considered the first-line treatment as hormonal anticancer drug. Unfortunately, LTZ develops osteoporosis as a main side effect which was overcome by using the co-administered; Zoledronic Acid (ZDA). Thus, there was a crucial need for this simultaneous quantification innovation, especially there were no any previously reported methods regarding both drugs together. In this study, an integrated framework was conducted between the experimental <em>analytical quality-by-design</em> (AQbD) approach and green analytical chemistry (GAC), emerging sensitive and robust RP-HPLC method. <em>Box-Behnken Design</em> was the developed model for optimizing an isocratic chromatographic separation on C<sub>18</sub> Equisil® ODS (4.6 × 250 mm, 5.0 μm) column at ambient temperature, using the mobile phase of 0.1 % aqueous trifluroacetic acid (pH 2.8): acetonitrile (54.5:45.5, v/v), at 1.0 mL/min flow rate with PDA detection at 254.0 nm and 210.0 nm for LTZ and ZDA, respectively. Model statistical and residual plots analysis was significant and normally distributed. Method was fully validated as per ICH guidelines, where good linearity was 0.20–10.00 µg/mL for both drugs in presence of Tadalafil (TDF) as an internal standard, obtaining adequate correlation coefficients <strong>(r)</strong> values. Calculated LOD results were 0.058 and 0.040 µg/mL while calculated LOQ results were 0.175 and 0.122 µg/mL for LTZ and ZDA, respectively. The proposed method was effectively applied on bulk, pharmaceutical dosage forms, and spiked human plasma. Statistical comparison of the anticipated results with the reported ones was performed. Greenness assessment was evaluated using Green Analytical Procedure Index (GAPI) and Analytical Greenness (AGREE) tools; where superiority results were achieved relative to other reported methods. Finally, an EVG method evaluation tool was assessed, and the attained results were represented through its radar chart.</p></div>","PeriodicalId":100822,"journal":{"name":"Journal of Pharmaceutical and Biomedical Analysis Open","volume":"4 ","pages":"Article 100036"},"PeriodicalIF":0.0000,"publicationDate":"2024-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949771X24000124/pdfft?md5=56ca2229de65e15d44a24040017a532d&pid=1-s2.0-S2949771X24000124-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Green analytical chemistry and quality by design: A combined approach towards simultaneous determination of Letrozole with its co-administered Zoledronic Acid for cancer patients\",\"authors\":\"Nourhan A. Abd El-Fatah ,&nbsp;Heba T. Elbalkiny ,&nbsp;Maha A. Hegazy ,&nbsp;Manal Mohammed Fouad ,&nbsp;Ghada M. El-Sayed\",\"doi\":\"10.1016/j.jpbao.2024.100036\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Nowadays, breast cancer is the most affecting and globally diagnosed malignancy among women, yet Letrozole (LTZ) was considered the first-line treatment as hormonal anticancer drug. Unfortunately, LTZ develops osteoporosis as a main side effect which was overcome by using the co-administered; Zoledronic Acid (ZDA). Thus, there was a crucial need for this simultaneous quantification innovation, especially there were no any previously reported methods regarding both drugs together. In this study, an integrated framework was conducted between the experimental <em>analytical quality-by-design</em> (AQbD) approach and green analytical chemistry (GAC), emerging sensitive and robust RP-HPLC method. <em>Box-Behnken Design</em> was the developed model for optimizing an isocratic chromatographic separation on C<sub>18</sub> Equisil® ODS (4.6 × 250 mm, 5.0 μm) column at ambient temperature, using the mobile phase of 0.1 % aqueous trifluroacetic acid (pH 2.8): acetonitrile (54.5:45.5, v/v), at 1.0 mL/min flow rate with PDA detection at 254.0 nm and 210.0 nm for LTZ and ZDA, respectively. Model statistical and residual plots analysis was significant and normally distributed. Method was fully validated as per ICH guidelines, where good linearity was 0.20–10.00 µg/mL for both drugs in presence of Tadalafil (TDF) as an internal standard, obtaining adequate correlation coefficients <strong>(r)</strong> values. Calculated LOD results were 0.058 and 0.040 µg/mL while calculated LOQ results were 0.175 and 0.122 µg/mL for LTZ and ZDA, respectively. The proposed method was effectively applied on bulk, pharmaceutical dosage forms, and spiked human plasma. Statistical comparison of the anticipated results with the reported ones was performed. Greenness assessment was evaluated using Green Analytical Procedure Index (GAPI) and Analytical Greenness (AGREE) tools; where superiority results were achieved relative to other reported methods. Finally, an EVG method evaluation tool was assessed, and the attained results were represented through its radar chart.</p></div>\",\"PeriodicalId\":100822,\"journal\":{\"name\":\"Journal of Pharmaceutical and Biomedical Analysis Open\",\"volume\":\"4 \",\"pages\":\"Article 100036\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-08-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2949771X24000124/pdfft?md5=56ca2229de65e15d44a24040017a532d&pid=1-s2.0-S2949771X24000124-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pharmaceutical and Biomedical Analysis Open\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2949771X24000124\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmaceutical and Biomedical Analysis Open","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949771X24000124","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

目前,乳腺癌是全球女性中发病率最高的恶性肿瘤,而来曲唑(LTZ)作为激素类抗癌药物被认为是一线治疗药物。遗憾的是,来曲唑的主要副作用是骨质疏松症,而通过联合使用唑来膦酸 (ZDA) 可以克服骨质疏松症。因此,这种同时定量的创新方法亟待开发,尤其是之前没有任何关于这两种药物同时使用的方法报道。在本研究中,在实验分析质量设计(AQbD)方法和绿色分析化学(GAC)之间建立了一个综合框架,形成了灵敏、稳健的 RP-HPLC 方法。采用盒-贝肯设计(Box-Behnken Design)模型优化了C18 Equisil® ODS (4.6 × 250 mm, 5.0 μm)色谱柱在常温下的等度色谱分离,流动相为0.1%三氟乙酸水溶液(pH 2.8):乙腈(54.5:45.5, v/v),流速为1.0 mL/min,PDA检测波长分别为254.0 nm和210.0 nm,LTZ和ZDA的检测波长分别为254.0 nm和210.0 nm。模型统计和残差图分析结果显著,且呈正态分布。根据 ICH 指南对该方法进行了全面验证,在以他达拉非(TDF)为内标时,两种药物的线性范围均为 0.20-10.00 µg/mL,获得了足够的相关系数(r)值。LTZ和ZDA的最低检出限(LOD)分别为0.058和0.040微克/毫升,最低定量限(LOQ)分别为0.175和0.122微克/毫升。所提出的方法有效地应用于散装、药物剂型和加标人体血浆。对预期结果和报告结果进行了统计比较。使用绿色分析程序指数(GAPI)和分析绿色度(AGREE)工具对绿色度进行了评估,结果优于其他已报道的方法。最后,对 EVG 方法评估工具进行了评估,并通过其雷达图来表示所取得的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Green analytical chemistry and quality by design: A combined approach towards simultaneous determination of Letrozole with its co-administered Zoledronic Acid for cancer patients

Nowadays, breast cancer is the most affecting and globally diagnosed malignancy among women, yet Letrozole (LTZ) was considered the first-line treatment as hormonal anticancer drug. Unfortunately, LTZ develops osteoporosis as a main side effect which was overcome by using the co-administered; Zoledronic Acid (ZDA). Thus, there was a crucial need for this simultaneous quantification innovation, especially there were no any previously reported methods regarding both drugs together. In this study, an integrated framework was conducted between the experimental analytical quality-by-design (AQbD) approach and green analytical chemistry (GAC), emerging sensitive and robust RP-HPLC method. Box-Behnken Design was the developed model for optimizing an isocratic chromatographic separation on C18 Equisil® ODS (4.6 × 250 mm, 5.0 μm) column at ambient temperature, using the mobile phase of 0.1 % aqueous trifluroacetic acid (pH 2.8): acetonitrile (54.5:45.5, v/v), at 1.0 mL/min flow rate with PDA detection at 254.0 nm and 210.0 nm for LTZ and ZDA, respectively. Model statistical and residual plots analysis was significant and normally distributed. Method was fully validated as per ICH guidelines, where good linearity was 0.20–10.00 µg/mL for both drugs in presence of Tadalafil (TDF) as an internal standard, obtaining adequate correlation coefficients (r) values. Calculated LOD results were 0.058 and 0.040 µg/mL while calculated LOQ results were 0.175 and 0.122 µg/mL for LTZ and ZDA, respectively. The proposed method was effectively applied on bulk, pharmaceutical dosage forms, and spiked human plasma. Statistical comparison of the anticipated results with the reported ones was performed. Greenness assessment was evaluated using Green Analytical Procedure Index (GAPI) and Analytical Greenness (AGREE) tools; where superiority results were achieved relative to other reported methods. Finally, an EVG method evaluation tool was assessed, and the attained results were represented through its radar chart.

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
自引率
0.00%
发文量
0
期刊最新文献
Recent advances in molecular imprinting techniques for the electrochemical analysis of chiral compounds A review for cortisol sensing in medical applications Preparation of novel semi-covalent molecularly imprinted polymer for highly improved adsorption performance of tetracycline in aqueous medium Development and validation of LC/MS/MS quantification method for plantaricins in culture supernatant Fabrication of ultra-sensitive and disposable electrochemical biosensor: Detection of kidney injury molecule-1 protein in urine for diagnosis of kidney injury
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1