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Stability indicating HPTLC method for quantitative estimation of manidipine sihydrochloride API

机译:稳定性表明HPTLC方法可定量评估盐酸马尼地平API

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A simple, selective, precise and stability indicating high performance thin layer chromatographic method has been established and validated for analysis of manidipine hydrochloride in bulk. The compound was analyzed on aluminium backed silica gel 60 F254 plates with methanokwater, 8.5:1.5 (v:v) as mobile phase. The system was found to give compact spots for manidipine dihydrochloride (R_F=0.75). Densitometric analysis was performed at 230 nm. Regression analysis data for the calibration plot indicated good linear relationships between response and concentration over the range of 500-3000 ng/spot The correlation coefficient, r~2 was 0.998. The values of slope and intercept of the calibration plot were 2785.5 and 62.314, respectively. The method was validated for precision, recovery and robustness. The limits of detection and quantification were 20 and 50 ng, respectively. Manidipine dihydrochloride was subjected to acid, base, peroxide and sunlight induced degradation. In stability test the drug was susceptible to acid and base hydrolysis, oxidation and photodegradation. Statistical analysis proved that the method is repeatable, selective and accurate for manidipine. Because the method could effectively separate the drug from their degradation products, it can be used as a stability indicating method.
机译:建立了一种简单,选择性,精确和稳定的指示性高效薄层色谱方法,并已验证可用于批量分析盐酸马尼地平。在铝支持的硅胶60 F254板上以8.5:1.5(v:v)的甲醇溶液作为流动相分析该化合物。发现该系统给出了马尼地平二盐酸盐的致密斑点(R_F = 0.75)。在230nm下进行光密度分析。校正图的回归分析数据表明,在500-3000 ng / spot范围内,响应与浓度之间具有良好的线性关系。相关系数r〜2为0.998。校准图的斜率和截距值分别为2785.5和62.314。验证了该方法的准确性,回收率和鲁棒性。检测限和定量限分别为20 ng和50 ng。使马尼地平二盐酸盐经受酸,碱,过氧化物和日光诱导的降解。在稳定性测试中,该药物易受酸和碱的水解,氧化和光降解作用。统计分析证明该方法对马尼地平具有可重复性,选择性和准确性。由于该方法可以有效地将药物与其降解产物分离,因此可以用作稳定性指示方法。

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