Analytical Chemistry Department, Faculty of Pharmacy, Egyptian Russian University, Cairo-Suez road, Badr City 11829, Egypt.
Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El-Aini street, 11562 Cairo, Egypt.
J Chromatogr Sci. 2021 Jan 14;59(2):140-147. doi: 10.1093/chromsci/bmaa088.
Two chromatographic methods were validated for the determination of the widely prescribed analgesic and antipyretic drug combination of paracetamol (PC) (recently integrated into the supportive treatment of COVID-19), propyphenazone (PZ) and caffeine (CF) in the presence of two PC impurities, namely 4-aminophenol and 4-nitrophenol. A "dual-mode" gradient high-performance liquid chromatography method was developed, where the separation was achieved via "dual-mode" gradient by changing both the ternary mobile phase composition (acetonitrile: methanol: water) and the flow rate. This enables a good resolution within a relatively shorter analysis time. The analysis was realized using Zorbax Eclipse XDB column C18, 5 μm (250 × 4.6 mm) and the UV detector was set at 220 nm. The other method is a thin-layer chromatography densitometry method, where the separation was achieved using a mobile phase composed of chloroform: toluene: ethyl acetate: methanol: acetic acid (6: 6: 1: 2: 0.1, by volume). Densitometric detection was performed at 220 nm on silica gel 60 F254 plates. The developed methods were fully validated as per the ICH guidelines and proved to be accurate, robust, specific and suitable for application as purity indicating methods for routine analysis of PC in pure form or in pharmaceuticals with PZ and CF in quality control laboratories.
两种色谱方法经过验证,可用于测定广泛应用的止痛和退热药物复方对乙酰氨基酚(PC)(最近被纳入 COVID-19 的支持性治疗)、丙苯酮(PZ)和咖啡因(CF),同时存在两种 PC 杂质,即 4-氨基酚和 4-硝基酚。开发了一种“双模式”梯度高效液相色谱法,通过同时改变三元流动相组成(乙腈:甲醇:水)和流速来实现“双模式”梯度分离。这使得在相对较短的分析时间内实现了良好的分辨率。分析采用 Zorbax Eclipse XDB 柱 C18,5 μm(250×4.6 mm),UV 检测器设置在 220 nm。另一种方法是薄层色谱密度计法,其中使用由氯仿:甲苯:乙酸乙酯:甲醇:乙酸(6:6:1:2:0.1,体积比)组成的流动相进行分离。在硅胶 60 F254 板上于 220 nm 处进行密度计检测。所开发的方法根据 ICH 指南进行了全面验证,证明其准确、稳健、专属性强,适用于作为纯度指示方法,用于在质量控制实验室中对纯形式的 PC 或含有 PZ 和 CF 的药物进行常规分析。