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首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >HPTLC Method for the Analysis of Melatonin in Bulk and Pharmaceutical Formulations
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HPTLC Method for the Analysis of Melatonin in Bulk and Pharmaceutical Formulations

机译:散装和药物制剂中褪黑激素分析的HPTLC方法

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摘要

A simple,precise and stability-indicating high perfor-.mance thin-layer chromatographic method of analysis of melatonin both as bulk drug and in pharmaceutical formulation was developed and validated.The method employed TLC aluminium plates precoated with silica gel 60F-254 as the stationary phase and mobile phase comprising toluene:ethyl acetate:formic acid (5:4.5:0.5 v/v).Densitometric analysis of melatonin was carried out in the absorbance mode at 290 nm.The linear regression analysis data for the calibration plots showed good linear relationship with r = 0.9989,with respect to peak area,in the concentration range 100-600 ng/ spot.The method was validated for precision,specificity,recovery and robustness.The recovery of the drug from tablets carried out by standard addition method was found to be 99.72 ± 0.682.Statistical analysis proves that the method is repeatable,selective and accurate for the estimation of the drug.Forced degradation studies showed the effect of variations in pH,UV light and high temperature on the stability of melatonin.As the proposed method could effectively separate the drug from its degradation products,it can be employed as a stability-indicating method.
机译:建立并验证了褪黑素作为原料药和药物制剂的简便,精确,稳定的高效薄层色谱分析方法。该方法采用涂有硅胶60F-254的TLC铝板作为色谱分离方法。包含甲苯:乙酸乙酯:甲酸(5:4.5:0.5 v / v)的固定相和流动相。褪黑素的密度分析在290 nm处以吸光度进行。线性回归分析数据表明校准曲线良好r = 0.9989的线性关系,相对于峰面积,在100-600 ng /点的浓度范围内。该方法的精密度,特异性,回收率和耐用性均得到验证。采用标准加法从片剂中回收药物实测值为99.72±0.682。统计分析证明该方法可重复,选择性,准确地估计药物的含量。强迫降解研究表明p变异的影响H,紫外线和高温对褪黑激素的稳定性有帮助。由于该方法可以有效地从降解产物中分离出药物,因此可以作为一种指示稳定性的方法。

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