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Spectral and polarographic determination of eprosartan. Kinetic studies of the oxidation of eprosartan using a platinum electrode.

机译:依普罗沙坦的光谱和极谱测定。使用铂电极氧化依普罗沙坦的动力学研究。

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摘要

Two simple and sensitive methods are presented for the determination of eprosartan in pharmaceutical preparations. The first method, spectrophotometry, was based on the oxidation of this drug by ammonium cerium (IV) nitrate in the presence of perchloric acid with subsequent measurement of the absorbance at 326 nm; this principle was adopted to develop a kinetic method for the determination of eprosartan in dosage forms. The second method, differential pulse polarography, was based on measuring the peak height at -1300 mV, corresponding to the reduction of the drug in Britton-Robinson buffer (pH 3). The proposed methods proved to be accurate and precise and can be applied for the routine analysis of this drug in commercial dosage forms, without interference from the excipients. The work was extended to study the electrochemical oxidation of eprosartan at different electrolysis currents (10-40 mA). The electrochemical decomposition products were characterized by UV/visible spectroscopy; the decompositionrates follow first order reactions and increase with raising the current. The degradation was found to be faster in basic than acidic medium. The thermodynamics for electrochemical decomposition were also evaluated at different pH values.
机译:提出了两种简单而灵敏的方法来测定药物制剂中依普罗沙坦的含量。第一种方法是分光光度法,其基础是在高氯酸存在下,硝酸铈铈(IV)将该药物氧化,然后测量326 nm的吸光度。采用该原理开发了一种测定剂型中依普罗沙坦的动力学方法。第二种方法,微分脉冲极谱法,是基于测量-1300 mV处的峰高,对应于Britton-Robinson缓冲液(pH 3)中药物的减少。所提出的方法被证明是准确和精确的,可用于商业剂型中该药物的常规分析,而不会受到赋形剂的干扰。研究工作扩展到研究依普罗沙坦在不同的电解电流(10-40 mA)下的电化学氧化。电化学分解产物通过紫外/可见光谱进行表征。分解速率遵循一阶反应,并随着电流的增加而增加。发现在碱性介质中降解要比在酸性介质中快。还评估了在不同pH值下电化学分解的热力学。

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