DEVELOPMENT AND VALIDATION OF VISIBLE SPECTROPHOTOMETRIC METHOD FOR ESTIMATION OF ELTROMBOPAG OLAMINE IN BULK AND TABLET DOSAGE FORM

Gangu Sreelatha, S. Rg, T. Harshana, Y. D. Spandana, Y. A. Reddy
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Abstract

A simple and sensitive visible spectrophotometric method has been developed for the quantitative estimation of Eltrombopag Olamine in its bulk and tablet dosage form. It is an orally active ethanolamine salt of Eltrombopag, a smallmolecule, nonpeptide thrombopoietin receptor agonist with megakaryopoiesis-stimulating activity. The maximum absorbance of drug was found at 425nm. Eltrombopag Olamine was found to be dissolved in Methanol so it was used as solvent for the conduction of work. Linearity range for the method was finalized as 3-18 μg/ml with R2 value of 0.9995. % RSD less than 2 which is well within indicates the method is precise and robust. The % recovery rate was found to be 100-101% indicating the method’s accuracy. The method was validated as per ICH guidelines provided and the results were found to be satisfactory. LOD & LOQ values were obtained as 0.150 & 0.456 respectively. Stability studies shows that the drug is unstable in various stress conditions like acid, base, water and oxidation.
建立和验证可见分光光度法测定散剂和片剂中艾曲波帕乙醇胺的含量
本研究建立了一种简单灵敏的可见分光光度法,用于定量测定散剂和片剂中的艾曲波帕乙醇胺。它是 Eltrombopag 的一种口服活性乙醇胺盐,是一种具有巨核细胞生成刺激活性的小分子、非肽类血小板生成素受体激动剂。药物的最大吸光度为 425 纳米。Eltrombopag Olamine 可溶解于甲醇,因此在工作中使用甲醇作为溶剂。该方法的线性范围最终确定为 3-18 μg/ml,R2 值为 0.9995。% RSD 小于 2,这表明该方法是精确和可靠的。回收率为 100-101%,表明该方法准确。根据 ICH 指南对该方法进行了验证,结果令人满意。LOD 和 LOQ 值分别为 0.150 和 0.456。稳定性研究表明,药物在酸、碱、水和氧化等各种压力条件下均不稳定。
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