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分析假冒药品和草药产品中的阿司匹林、普拉格雷和氯吡格雷:Plackett-Burman 筛选和 Box-Behnken 优化。

Analysis of Aspirin, Prasugrel and Clopidogrel in Counterfeit Pharmaceutical and Herbal Products: Plackett-Burman Screening and Box-Behnken Optimization.

机构信息

Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El-Aini St., Cairo 11562, Egypt.

Supreme Board of Drugs and Medical Appliances, Ministry of Health and Population, Aden 6022, Yemen.

出版信息

J Chromatogr Sci. 2021 Aug 18;59(8):730-747. doi: 10.1093/chromsci/bmaa113.

DOI:10.1093/chromsci/bmaa113
PMID:33367531
Abstract

An isocratic reversed-phase high-performance liquid chromatographic method has been developed and validated for the simultaneous determination of aspirin, prasugrel HCl and clopidogrel bisulfate in the presence of clopidogrel-related compound (impurity-A) in focus on counterfeit. This method was used to determine counterfeited antiplatelet drugs in two substandard Indian pharmaceutical products sold on the market in Yemen and two traditional herbal medicines sold on the market in China. Thin layer chromatography and mass spectrometry of counterfeit herbal medicines have additionally been carried out to verify the identification of adulterants. Chromatographic separation was performed on Inertsil ® ODS-3 C18 (4.6 × 250 mm, 5 μm) with isocratic mobile phase elution containing a mixture of acetonitrile: (25 mM) potassium dihydrogen phosphate buffer, pH 2.7 adjusted with 0.1 M o-phosphoric acid (79: 21, v/v), at a flow rate of 1 mL/min and UV detection at 220 nm. Designs of experiment methodology, Plackett-Burman and Box-Behnken designs were used for the screening and optimization of the mobile phase composition. The method validation was also performed in accordance with the International Council on Harmonization (ICH) guidelines. The method developed for routine analysis was found to be sensitive, simple, accurate and highly robust. The results were statistically compared to reference methods using Student's t-test and variance ratio F-test at P < 0.05.

摘要

已开发并验证了一种等度反相高效液相色谱法,用于在关注假冒产品中同时测定阿司匹林、普拉格雷盐酸盐和氯吡格雷硫酸氢盐,以及氯吡格雷相关化合物(杂质 A)。该方法用于测定在也门市场上销售的两种不合格印度药品和在中国市场上销售的两种传统草药中的假冒抗血小板药物。还对假冒草药进行了薄层色谱和质谱分析,以验证杂质的鉴定。色谱分离在 Inertsil ® ODS-3 C18(4.6×250mm,5μm)上进行,采用等度流动相洗脱,包含乙腈:(25mM)磷酸二氢钾缓冲液,pH 2.7,用 0.1M 邻磷酸调至 79:21(v/v),流速为 1mL/min,在 220nm 处进行紫外检测。实验设计方法、Plackett-Burman 和 Box-Behnken 设计用于筛选和优化流动相组成。该方法还按照国际协调会议(ICH)指南进行了验证。为常规分析开发的方法被发现灵敏、简单、准确且高度稳健。使用学生 t 检验和方差比 F 检验对结果进行统计学比较,置信度为 P < 0.05。

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