A. Naggar, Elnasr Tas, S. As, A. Kotb, El Sayed Aay
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引用次数: 10
摘要
建立了三种简便、选择性好、准确度高、精密度高的分光光度法测定盐酸甲氧氯普胺(MCP)的方法。第一种方法(方法A)是将重氮化的MCP与2,5-二苯基-2,4-二氢吡唑-3-酮(DPP)在碱性介质中偶联反应生成偶氮染料。第二种方法(方法B)是基于MCP与4-羟基苯甲醛(HBD)之间的席夫碱生成反应。最后一种方法(方法C)是基于MCP与伊红Y (ESN)反应形成有色离子对络合物。方法A、方法B和方法C在浓度为1.35 ~ 40.37、1.01 ~ 5.05和1.01 ~ 10.09 μg/mL MCP(426、386和543 nm)范围内符合比尔定律,摩尔吸光度分别为1.51×104 L mol-1 cm-1、2.10×104 L mol-1 cm-1和3.34×104 L mol-1 cm-1。该方法成功地应用于药物制剂中MCP的测定,不受常用辅料的干扰。
Determination of Metoclopramide Hydrochloride in Pharmaceutical Formulations Using Three Different Spectrophotometric Methods
Three simple, selective, accurate and precise spectrophotometric methods were developed for the determination of Metoclopramide Hydrochloride (MCP) in dosage forms. The first method (Method A) is based on coupling reaction of diazotized MCP with 2,5-diphenyl-2,4-dihydro-pyrazol-3-one (DPP) in alkaline medium to form azo dye. The second method (Method B) is based on Schiff’s base formation reaction between MCP and 4-hydroxybenzaldehyde (HBD). The last method (Method C) is based on the formation of colored ion–pair complex from the reaction of MCP with Eosin Y (ESN). Beer’s law was obeyed in the concentration range of 1.35-40.37, 1.01-5.05 and 1.01-10.09 μg/mL MCP at 426, 386 and 543 nm with molar absorptivity of 1.51×104 L mol-1 cm-1, 2.10×104 L mol-1 cm-1 and 3.34×104 L mol-1 cm-1 for Method A, Method B and Method C, respectively. The proposed methods were successfully applied to the determination of MCP in pharmaceutical preparations without any interference from common excipients.