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Complexity in Estimation of Esomeprazole and its Related Impurities’ Stability in Various Stress Conditions in Low-Dose Aspirin and Esomeprazole Magnesium Capsules

机译:低剂量阿司匹林和埃索美拉唑镁胶囊在不同应激条件下估算埃索美拉唑的复杂性及其相关杂质的稳定性

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摘要

A complex, sensitive, and precise high-performance liquid chromatographic method for the profiling of impurities of esomeprazole in low-dose aspirin and esomeprazole capsules has been developed, validated, and used for the determination of impurities in pharmaceutical products. Esomeprazole and its related impurities' development in the presence of aspirin was traditionally difficult due to aspirin's sensitivity to basic conditions and esomeprazole's sensitivity to acidic conditions. When aspirin is under basic, humid, and extreme temperature conditions, it produces salicylic acid and acetic acid moieties. These two byproducts create an acidic environment for the esomeprazole. Due to the volatility and migration phenomenon of the produced acetic acid and salicylic acid from aspirin in the capsule dosage form, esomeprazole's purity, stability, and quantification are affected. The objective of the present research work was to develop a gradient reversed-phase liquid chromatographic method to separate all the degradation products and process-related impurities from the main peak. The impurities were well-separated on a RP8 column (150 mm × 4.6mm, X-terra, RP8, 3.5μm) by the gradient program using a glycine buffer (0.08 M, pH adjusted to 9.0 with 50% NaOH), acetonitrile, and methanol at a flow rate of 1.0 mL min~(-1) with detection wavelength at 305 nm and column temperature at 30℃. The developed method was found to be specific, precise, linear, accurate, rugged, and robust. LOQ values for all of the known impurities were below reporting thresholds. The drug was subjected to stress conditions of hydrolysis, oxidation, photolysis, and thermal degradation in the presence of aspirin. The developed RP-HPLC method was validated according to the present ICH guidelines for specificity, linearity, accuracy, precision, limit of detection, limit of quantification, ruggedness, and robustness.
机译:已开发,验证了一种复杂,灵敏,精确的高效液相色谱方法,用于分析低剂量阿司匹林和埃索美拉唑胶囊中埃索美拉唑的杂质,并用于测定药品中的杂质。传统上由于阿司匹林对碱性条件的敏感性和埃索美拉唑对酸性条件的敏感性,在阿司匹林存在下埃索美拉唑及其相关杂质的发展历来是困难的。当阿司匹林处于碱性,潮湿和极端温度条件下时,会产生水杨酸和乙酸部分。这两种副产物为埃索美拉唑创造了酸性环境。由于胶囊剂型中由阿司匹林产生的乙酸和水杨酸具有挥发性和迁移现象,因此埃索美拉唑的纯度,稳定性和定量受到影响。本研究工作的目的是开发一种梯度反相液相色谱方法,以从主峰中分离出所有降解产物和与过程相关的杂质。使用甘氨酸缓冲液(0.08 M,pH值用50%NaOH调节至9.0),乙腈,通过梯度程序在RP8色谱柱(150 mm×4.6mm,X-terra,RP8,3.5μm)上将杂质充分分离。甲醇的流速为1.0 mL min〜(-1),检测波长为305 nm,柱温为30℃。发现所开发的方法是特定的,精确的,线性的,准确的,坚固的和耐用的。所有已知杂质的LOQ值均低于报告阈值。在阿司匹林的存在下,该药物经受了水解,氧化,光解和热降解的胁迫条件。根据目前的ICH指南验证了开发的RP-HPLC方法的特异性,线性,准确性,精密度,检测限,定量限,坚固性和耐用性。

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