纯和剂型特拉唑嗪的电化学测定

K. G. Kumar, S. John, R. Poduval, P. Augustine
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引用次数: 5

摘要

目前已建立了两种测定纯特拉唑嗪和剂型特拉唑嗪的方法,一种是电位传感器法,另一种是伏安法。将特拉唑辛-硅钨酸离子缔合物作为离子载体用于电位传感器的制备。该方法的最佳浓度范围为7 × 10^(-2) ~ 8 × 10^(-4) M。该体系在pH 4.2条件下具有完美的纳恩斯蒂斜率(59.3 mV / 10年),几乎不受普通阳离子和阴离子的干扰。在-100 ~ +100 mV的电势范围内,在开关电势为800 mV的玻璃碳电极上,对该药物进行了循环和线性扫描伏安研究。以氢氧化钠为支撑电解质时,在774 mV的电压下,药物出现了一个明确的不可逆阳极峰。研究了扫描速率和浓度对电流的影响,并在此基础上建立了伏安法定量测定该药物。两种方法均应用于两种市售片剂中该药的含量测定,结果精密度高,准确度高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrochemical Determination of Terazosin in Pure Form and in Dosage Forms
Two methods have been developed for the determination of terazosin in pure form and in dosage forms- one based on a potentiometric sensor and the other a voltammetric technique. Terazosin-silicotungstic acid ion-association is developed as an ionophore in the fabrication of the potentiometric sensor. The optimum concentration range of the developed method was 7 x 10^(-2) to 8 X 10^(-4) M of the drug. The system gave a perfectly Nernstian slope (59.3 mV per decade) in the pH 4.2 with hardly any interference from the common cations and anions. The cyclic and linear sweep voltammetric studies of the drug on a glassy carbon electrode in the potential range -100 to +100 mV with a switching potential of 800 mV have also been carried out. The drug gave a well-defined irreversible anodic peak at 774 mV when sodium hydroxide was used as the supporting electrolyte. Influence of scan rate and concentration on current were studied and based on this, a voltammetric method has also been developed for the quantitative determination of the drug. Both the methods have been applied for the determination of the drug in two commercially available tablets and the results are highly precise and accurate.
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