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首页> 外文期刊>Journal of food and drug analysis >Extractive Spectrophotometric Determination of Cetirizine Dihydrochloride in Pure and Pharmaceutical Preparations
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Extractive Spectrophotometric Determination of Cetirizine Dihydrochloride in Pure and Pharmaceutical Preparations

机译:萃取和分光光度法测定纯和药物制剂中盐酸西替利嗪的含量

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摘要

A simple and sensitive extractive spectrophotometric method has been described for the assay of cetirizine dihydrochloride in pure and different pharmaceutical preparations. The method was based on the formation of the ion-pair complex from the reaction between cetirizine dihydrochloride and methyl orange in pH 4.0, which gave a yellow color after chloroform extraction and exhibited a maximum absorbance at 424.5 nm. Beer's law was obeyed in the concentration range of 2.5 - 20 mug/mL. The method was tested and validated for various parameters according to ICH guidelines. The detection and quantification limits were 1.0 and 3.0 mug/mL, respectively. The proposed method was successfully applied for the determination of cetirizine dihydrochloride in pharmaceutical preparations. The results demonstrated that the procedure was accurate, precise and reproducible while statistical analysis of the obtained results showed no significant difference between the proposed method and reference method. No interference was observed for common pharmaceutical preparations.
机译:已经描述了一种简单灵敏的萃取分光光度法,用于测定纯和不同药物制剂中盐酸西替利嗪的含量。该方法基于西替利嗪二盐酸盐与甲基橙在pH 4.0下的反应形成的离子对络合物,氯仿萃取后呈黄色,在424.5 nm处显示最大吸光度。在2.5-20杯/毫升的浓度范围内遵守比尔定律。根据ICH指南对该方法的各种参数进行了测试和验证。检出限和定量限分别为1.0和3.0杯/毫升。该方法已成功地用于药物制剂中盐酸西替利嗪的测定。结果表明该方法准确,准确且可重复,而对所得结果的统计分析表明,该方法与参考方法之间无显着差异。普通药物制剂未见干扰。

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