Spectrophotometric Determination of Nicorandil in Bulk andPharmaceutical Formulation Using Phospho-Molybdenum Blue Complex

S. El-Adl, M. El-Sadek, Saeed Nm
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引用次数: 2

Abstract

A new spectrophotometric method is described for the determination of nicorandil in bulk and pharmaceutical dosage form. It is based on the reduction of nitrate in nicorandil to nitrite ion by using vanadium chloride, and reduction of phosphomolybdic acid to phospho-molybdenum blue complex by sodium sulfide, phospho-molybdenum blue complex is then oxidized by nitrite ion leading to a decrease in blue color intensity which found to be directly proportional to the concentration of nicorandil. Maximum absorbance was measured at 827 nm. Effect of acidity, volume of Sodium Sulfide, stability of complex, volume of vanadium chloride, time and temperature of the reaction were completely studied. The proposed method was satisfactorily applied for the determination of the drug in both bulk and pharmaceutical forms, the calibration curve was linear over the range (60–200 μg/ml) and the results were compared statistically with reference methods.
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磷钼蓝配合物分光光度法测定原料药和制剂中尼可地尔的含量
介绍了一种新的分光光度法测定原料药和制剂中尼可地尔的含量。它的原理是用氯化钒将尼科地尔中的硝酸盐还原为亚硝酸盐离子,用硫化钠将磷钼酸还原为磷钼蓝配合物,磷钼蓝配合物再被亚硝酸盐离子氧化,导致蓝色强度的降低,而蓝色强度与尼科地尔的浓度成正比。在827 nm处测得最大吸光度。研究了酸度、硫化钠体积、配合物稳定性、氯化钒体积、反应时间和温度等因素对反应的影响。该方法在60 ~ 200 μg/ml范围内具有良好的线性关系,可用于原料药和制剂的测定,并与参考方法进行了统计学比较。
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