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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Utility of the Ion-Pair Formation for Spectrophotometric Determination of Terfenadine in Pure Form and in Some Pharmaceutical Formulations
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Utility of the Ion-Pair Formation for Spectrophotometric Determination of Terfenadine in Pure Form and in Some Pharmaceutical Formulations

机译:离子对形成用于分光光度法测定纯品形式和某些药物制剂中的苯达那定的实用性

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摘要

A spectrophotometric procedure for the determination of terfenadine and a number of its pharmaceutical preparations has been developed that offers advantages of simplicity, rapidity, sensitivity and stability indication over the official USP (1995) method. The proposed method is based on the formation of ion-pairs by the reaction of terfenadine with some chromotropic acid mono- and bis-azo dyes. Different variables affecting the ion-pair formation were studied and optimized. At the maximum absorption of 557, 521, 592 and 543 nm, Beer's law is obeyed in the range 0.2-18.6, 0.2-16.4, 0.2-25.0 and 0.2-22.2 #mu#g ml~(-1) on using reagents I, II, III and IV, respectively. The stoichiometric ratio and stability of each ion-pair were estimated and the mechanism of the reaction is discussed. The molar absorptivity and Sandell sensitivity of the produced ion-pairs were calculated in addition to Ringbom optimum concentration ranges. Statistical treatment of the experimental results indicates that the procedures are precise and accurate. Excipients used as additives in pharmaceutical formulations did not interfere in the proposed procedures. The reliability of the methods was established by parallel determination against the official USP method. The procedures described were successfully applied to the determination of the bulk drug and its pharmaceutical formulations by applying the standard addition technique.
机译:已经开发出一种用于测定特非那定及其许多药物制剂的分光光度法,与官方的USP(1995)方法相比,该方法具有简便,快速,灵敏和稳定的指示优势。所提出的方法基于特非那定与某些变色酸单偶氮和双偶氮染料的反应形成离子对。研究和优化了影响离子对形成的不同变量。在使用试剂I的情况下,在557、521、592和543 nm的最大吸收下,遵循比尔定律在0.2-18.6、0.2-16.4、0.2-25.0和0.2-22.2#mu#g ml〜(-1)范围内,II,III和IV。估算了每个离子对的化学计量比和稳定性,并讨论了反应机理。除林宝最佳浓度范围外,还计算了产生的离子对的摩尔吸收率和桑德尔灵敏度。实验结果的统计处理表明该程序是精确的。在药物制剂中用作添加剂的赋形剂不会干扰建议的程序。该方法的可靠性是通过与官方USP方法平行确定的来确定的。所描述的程序通过应用标准添加技术成功地应用于了原料药及其药物制剂的测定。

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