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首页> 外文期刊>Indian journal of pharmaceutical sciences. >Anodic Oxidation of Etodolac and its Linear Sweep, Square Wave and Differential Pulse Voltammetric Determination in Pharmaceuticals
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Anodic Oxidation of Etodolac and its Linear Sweep, Square Wave and Differential Pulse Voltammetric Determination in Pharmaceuticals

机译:依托多拉克的阳极氧化及其线性扫描,方波和差分脉冲伏安法测定

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摘要

In this study, simple, fast and reliable cyclic voltammetry, linear sweep voltammetry, square wave voltammetry and differential pulse voltammetry methods were developed and validated for determination of etodolac in pharmaceutical preparations. The proposed methods were based on electrochemical oxidation of etodolac at platinum electrode in acetonitrile solution containing 0.1 M lithium perchlorate. The well-defined oxidation peak was observed at 1.03 V. The calibration curves were linear for etodolac at the concentration range of 2.5-50 mu g/ml for linear sweep, square wave and differential pulse voltammetry methods, respectively. Intra-and inter-day precision values for etodolac were less than 4.69, and accuracy (relative error) was better than 2.00%. The mean recovery of etodolac was 100.6% for pharmaceutical preparations. No interference was found from three tablet excipients at the selected assay conditions. Developed methods in this study are accurate, precise and can be easily applied to Etol, Tadolak and Etodin tablets as pharmaceutical preparation.
机译:在这项研究中,开发了简单,快速和可靠的循环伏安法,线性扫描伏安法,方波伏安法和差分脉冲伏安法,并已验证了该方法可用于测定药物制剂中的依托度酸。所提出的方法基于乙二胺四乙酸在含有0.1 M高氯酸锂的乙腈溶液中在铂电极上的电化学氧化。在1.03 V处观察到明确定义的氧化峰。对于线性扫描,方波和差分脉冲伏安法,依托度酸的校正曲线在2.5-50μg / ml的浓度范围内均为线性。依托度酸的日内和日间精度值均小于4.69,并且精度(相对误差)优于2.00%。药物制剂中依托度酸的平均回收率为100.6%。在选定的测定条件下,未从三种片剂赋形剂中发现干扰。本研究中开发的方法准确,精确,可以轻松地作为药物制剂应用于Etol,Tadolak和Etodin片剂。

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