Simultaneously quantifying a novel five-component anti- migraine formulation containing ergotamine, propyphenazone, caffeine, camylofin, and mecloxamine using UV spectrophotometry and chemometric models

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Ahmed Emad F. Abbas, Nahla A. Abdelshafi, Mohammed Gamal, Michael K. Halim, Basmat Amal M. Said, Ibrahim A. Naguib, Mohmeed M. A. Mansour, Samir Morshedy, Yomna A. Salem
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Abstract

This study presents a new method for simultaneously quantifying a complex anti-migraine formulation containing five components (ergotamine, propyphenazone, caffeine, camylofin, and mecloxamine) using UV spectrophotometry and chemometric models. The formulation presents analytical challenges due to the wide variation in component concentrations (ERG: PRO: CAF: CAM: MEC ratio of 0.075:20:8:5:4) and highly overlapping UV spectra. To create a comprehensive validation dataset, the Kennard-Stone Clustering Algorithm was used to address the limitations of arbitrary data partitioning in chemometric methods. Three different chemometric models were evaluated: Classical Least Squares (CLS), Partial Least Squares (PLS), and Multivariate Curve Resolution-Alternating Least Squares (MCR-ALS). Among these, MCR-ALS demonstrated excellent performance, achieving recovery values of 98–102% for all components, accompanied by minimal root mean square errors of calibration (0.072–0.378) and prediction (0.077–0.404). Moreover, the model exhibited high accuracy, with relative errors ranging from 1.936 to 3.121%, bias-corrected mean square errors between 0.074 and 0.389, and a good sensitivity (0.2097–1.2898 μg mL−1) for all components. The Elliptical Joint Confidence Region analysis further confirmed the predictive performance of the models, with MCR-ALS consistently showing the smallest ellipses closest to the ideal point (slope = 1, intercept = 0) for most analytes, indicating superior accuracy and precision. The approach's sustainability was rigorously assessed using six advanced metrics, validating its environmental friendliness, economic viability, and practical application. This approach effectively resolves complex pharmaceutical formulations, contributing to sustainable development objectives in quality control processes.

利用紫外分光光度法和化学计量学模型同时量化含有麦角胺、异丙嗪、咖啡因、骆驼蓬素和麦考酚胺的新型五组分抗偏头痛制剂
本研究提出了一种新方法,利用紫外分光光度法和化学计量学模型,同时对含有五种成分(麦角胺、丙菲那宗、咖啡因、骆驼蓬素和麦考酚胺)的复杂抗偏头痛制剂进行定量。该制剂的成分浓度变化很大(ERG: PRO: CAF: CAM: MEC 的比例为 0.075:20:8:5:4),且紫外光谱高度重叠,这给分析带来了挑战。为了创建一个全面的验证数据集,我们使用了 Kennard-Stone 聚类算法来解决化学计量学方法中任意数据分区的局限性。对三种不同的化学计量模型进行了评估:经典最小二乘法(CLS)、部分最小二乘法(PLS)和多变量曲线解析-替代最小二乘法(MCR-ALS)。其中,MCR-ALS 表现出色,所有成分的回收率都达到 98-102%,校准均方根误差(0.072-0.378)和预测均方根误差(0.077-0.404)都很小。此外,该模型的准确度也很高,相对误差在 1.936% 到 3.121% 之间,偏差校正均方误差在 0.074 到 0.389 之间,对所有成分的灵敏度(0.2097-1.2898 μg mL-1)都很高。椭圆联合置信区分析进一步证实了模型的预测性能,对于大多数分析物,MCR-ALS 始终显示出最接近理想点(斜率 = 1,截距 = 0)的最小椭圆,表明其准确度和精确度都很高。该方法的可持续性通过六项先进指标进行了严格评估,验证了其环境友好性、经济可行性和实际应用性。该方法可有效解决复杂的药物制剂问题,有助于实现质量控制过程中的可持续发展目标。
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来源期刊
BMC Chemistry
BMC Chemistry Chemistry-General Chemistry
CiteScore
5.30
自引率
2.20%
发文量
92
审稿时长
27 weeks
期刊介绍: BMC Chemistry, formerly known as Chemistry Central Journal, is now part of the BMC series journals family. Chemistry Central Journal has served the chemistry community as a trusted open access resource for more than 10 years – and we are delighted to announce the next step on its journey. In January 2019 the journal has been renamed BMC Chemistry and now strengthens the BMC series footprint in the physical sciences by publishing quality articles and by pushing the boundaries of open chemistry.
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