在 C12 和 C14 同系物存在的情况下同步量化抗胆碱能药物的尖端 HPLC 和 MCR 技术:绿色和白色化学的可靠应用。

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL Archiv der Pharmazie Pub Date : 2024-06-18 DOI:10.1002/ardp.202400256
Asma S. Al-Wasidi, Hoda A. Ahmed, Manal Falag Abtan Alshammari, Sherif S. Nafee, Mahmoud A. Mohamed
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引用次数: 0

摘要

绿色化学和白色化学在提高可持续性和效率方面具有无与伦比的潜力,对化学工业的变革至关重要。本研究开发了九种绿色和白色可持续发展工具,包括绿色分析程序指数(GAPI)、复杂分析程序指数(ComplexGAPI)、分析绿色度、样品制备分析绿色度指标、分析生态尺度(ESA)、分析方法绿色度评分、高效液相色谱-环境评估工具(HPLC-EAT)、分析方法体积强度和蓝色适用性等级指数(BAGI)、该工具采用了创新的、直接的比值谱均值中心法(MCR)和反相高效液相色谱法(RP-HPLC),用于同时分析和分离纯眼药水中的环戊丙酸(CYC)和苯扎氯铵(BNZ)的 C12 和 C14 同系物。流动相为缓冲磷酸盐和乙腈(35:65, v/v),pH 值调至 6.3,紫外检测波长为 215nm。实验流速为 2.0 mL min-1,分析柱为 L11 Inertsil Ph-3(150 mm × 4.6 mm,5 µm)。所有序列均在 25°C 的柱温箱中运行。MCR 方法有效地解决了药物光谱重叠的问题。CYC 和 BNZ 分别在 227.5 和 220.4 纳米波长处采用了这种方法。作为高效液相色谱分析的一部分,采用了等度方法,流动相为磷酸盐缓冲液和乙腈,比例为 35:65。在所有药物的 20-320 µg mL-1 和 5-30 µg mL-1 范围内,HPLC 和 MCR 方法的校准曲线之间的相关系数均大于 0.999。该技术的初次回收率非常高,从 97.2% 到 100.5%。推荐的方法已根据国际协调理事会的指导方针进行了验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Cutting-edge HPLC and MCR techniques for synchronically quantifying anticholinergic drugs in the presence of C12 and C14 homologs: Robust application to green and white chemistry

Green and white chemistry are vital to revolutionizing the chemical industry through their unparalleled potential to enhance sustainability and efficiency. In this study, nine sustainability tools of both green and white metrics, including green analytical procedure index (GAPI), ComplexGAPI, analytical greenness, analytical greenness metric for sample preparation, Analytical Eco-Scale (ESA), analytical method greenness score, high-performance liquid chromatography- environmental assessment tool (HPLC-EAT), analytical method volume intensity, and blue applicability grade index (BAGI), have been developed for appraising environmental friendliness for both innovative and straightforward mean centering of ratio spectra (MCR) and reversed-phase high-performance liquid chromatography (RP-HPLC) strategies utilized for concurrent analysis and separation of cyclopentolate (CYC) and C12 and C14 homologs of benzalkonium chloride (BNZ) in pure and ophthalmic solution. The mobile phase, formed of buffer phosphate and acetonitrile (35:65, v/v), was adjusted to pH 6.3, and 215-nm UV detection was used. The experimental flow rate was 2.0 mL min−1, and the analytical column was L11 Inertsil Ph-3 (150 mm × 4.6 mm, 5 µm). All sequences were run at 25°C in the column oven. The MCR approach effectively resolved the drug's spectral overlapping. CYC and BNZ employed this approach at 227.5 and 220.4 nm, respectively. As part of the HPLC analysis, an isocratic method was employed with phosphate buffer and acetonitrile in the mobile phase at 35:65. A correlation coefficient greater than 0.999 was observed between the calibration curves for the HPLC and MCR methods in the ranges of 20–320 µg mL−1 and 5–30 µg mL−1 for all drugs. The technique yields excellent primary recovery rates, ranging from 97.2% to 100.5%. The recommended approach has been validated according to International Council for Harmonization guidelines.

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来源期刊
Archiv der Pharmazie
Archiv der Pharmazie 医学-化学综合
CiteScore
7.90
自引率
5.90%
发文量
176
审稿时长
3.0 months
期刊介绍: Archiv der Pharmazie - Chemistry in Life Sciences is an international journal devoted to research and development in all fields of pharmaceutical and medicinal chemistry. Emphasis is put on papers combining synthetic organic chemistry, structural biology, molecular modelling, bioorganic chemistry, natural products chemistry, biochemistry or analytical methods with pharmaceutical or medicinal aspects such as biological activity. The focus of this journal is put on original research papers, but other scientifically valuable contributions (e.g. reviews, minireviews, highlights, symposia contributions, discussions, and essays) are also welcome.
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