Indirect Spectrophotometric Method for Determination of Methyldopa in Pure and Pharmaceutical Formulation

S. Fathi
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Abstract

Sensitive and accurate spectrophotometric method for the assay of methyldopa (MeD) as pure form and in it is formulations. The method was centred on the oxidation of methyldopa drug with Fe+2ions. The free Fe+2 ions react with 4,7-diphenyl-1,10-phenanthroline chromogenic reagent. In the method, the formed Ferron complex is colorimetrically can be monitored at 533 nm versus reagent blank. The linear relationship between various MeD concentrations versus absorbance for each concentration was in the range of 0.25-2.5 μg.mL-1 with molar absorptivity 1.3272x105 L.mol-1.cm-1 for the method. The determination coefficient (R2) was found to be 0.9902, and the limit of detection (LOD) and limit of quantification(LOQ) were 0.011μg.ml-1and 0.036 μg.ml-1, respectively. The percent recovery from 99.84% to 102.40 %. The suggested procedure could be used for the estimation of MeD in dosage forms (two types of tablets from two companies) with satisfactory results.
间接分光光度法测定纯制剂和制剂中甲基多巴的含量
建立了一种灵敏、准确的测定甲基多巴(MeD)纯度及其制剂的分光光度法。该方法以铁离子氧化甲基多巴药物为中心。游离铁+2离子与4,7-二苯基-1,10-菲罗啉显色试剂反应。在该方法中,形成的铁配合物可以在533 nm处与试剂空白进行比色监测。各浓度与吸光度的线性关系在0.25 ~ 2.5 μg范围内。摩尔吸光度为1.3272 × 105 L.mol-1。Cm-1为方法。测定系数(R2)为0.9902,检测限(LOD)和定量限(LOQ)均为0.011μg。ml-1和0.036 μg。分别ml-1。回收率为99.84% ~ 102.40%。所建议的方法可用于估算剂型(两家公司的两种片剂)的MeD,结果令人满意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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