硝酸铈铵存在下1,5-二氨基萘氧化偶联分光光度法测定纯制剂和药物中的甲基多巴

Noor Mansoor Ghaib Allah, A. Ahmed, Nashwan O. Tapabashi
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引用次数: 1

摘要

氧化偶联反应是用于评估药物制剂中某些药物的重要方法之一。本研究描述了一种快速灵敏的光谱方法的发展,该方法考虑了酸性水溶液中痕量甲基多巴的测定。所采用的方法集中在氧化偶联上,因为药物甲基多巴与试剂1,5-二氨基萘在硝酸铈(IV)铵作为氧化剂的存在下形成稳定的蓝色产物,在730nm处产生最高吸收。该产物在(5.4-39.6)µg/ml的范围内符合比尔定律,摩尔吸光系数为4.79471×104L/mol。厘米Sandell′sindex,0。0044µg/cm2,相对标准偏差在(0.5942-0.9687)%范围内,平均回收率和测定因子分别为99.908%和0.9998
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Spectrophotometric Determination of Methyldopa in Pure and Pharmaceutical Preparations by the Oxidative Coupling Reaction with 1, 5-Diaminonaphthalene in the Presence of Ammonium Ceric (IV) Nitrate
Oxidative coupling reactions are one of the significant methods used in the estimation of certain drugs in pharmaceutical formulations. This study describes the development of a fast and sensitive spectroscopic method considering the determination of trace amounts of methyldopa in an acidic aqueous solution. The adopted method centered on oxidative coupling due to the drug Methyldopa with the reagent 1, 5-diaminonaphthalene in the presence of ceric (IV) ammonium nitrate as oxidizing agent to form a stable blue-colored product, giving the highest absorption at 730 nm. The product was appeared to agree Beer’s law within the limits of (5.4 - 39.6) µ g /ml, and a value of molar absorptivity equal to 4.79471 × 10 4 L / mol . cm . Sandell ′ sindex , 0 . 0044 µ g/ cm 2 , Relative standard deviation was in the range (0.5942 - 0.9687)%, whereas recovery average and determination factor were 99.908% and 0.9998
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