Structural identification and estimation of Rosuvastatin calcium related impurities in Rosuvastatin calcium tablet dosage form

Chamarthi R.P. Kishore, G.V. Krishna Mohan
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引用次数: 13

Abstract

A precise, accurate, specific, linear, rugged and robust analytical method was developed and validated for estimation of process and degradant impurities of Rosuvastatin calcium (RSC) in Rosuvastatin calcium tablets. 150 mm length column, 4.6 mm diameter and 3.5μ particle size with C18 stationary phase and pH3.0 phosphate buffer as mobile phase. Column was maintained at 30 °C.All impurities are monitored at 248 nm.Impurities are separated in gradient elution mode. All degradant impurities of RSC (Anti-isomer, 5-ketoacid, lactone and meglumine adduct), process impurity (Imp-A) are well separated. Unknown impurity (Meglumine adduct) formed during stability studies was isolated using preparative HPLC and structure was characterized by NMR and Mass spectrometry (LC-MS and HRMS) studies. Method is capable of separating and estimating all the degradant and process impurities.

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瑞舒伐他汀钙片剂型中瑞舒伐他汀钙相关杂质的结构鉴定与评价
建立了瑞舒伐他汀钙片中瑞舒伐他汀钙(RSC)的工艺及降解杂质的定量分析方法,并进行了验证。柱长150mm,柱径4.6 mm,粒径3.5μ,以C18固定相和pH3.0磷酸盐缓冲液为流动相。柱保持在30°C。所有杂质都在248纳米处监测。以梯度洗脱的方式分离杂质。RSC的所有降解杂质(抗异构体、5-酮酸、内酯和三聚氰胺加合物)和工艺杂质(Imp-A)都得到了很好的分离。稳定性研究过程中形成的未知杂质(Meglumine加合物)采用制备型高效液相色谱(HPLC)分离,结构采用NMR和质谱(LC-MS和HRMS)研究。该方法能够分离和估计所有降解和工艺杂质。
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