Yilmaz B, Kaban S, Akcay B K
Department of Analytical Chemistry, Faculty of Pharmacy, Ataturk University, 25240 Erzurum, Turkey.
Indian J Pharm Sci. 2015 Jul-Aug;77(4):413-21. doi: 10.4103/0250-474x.164777.
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 μg/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.
在本研究中,开发并验证了简单、快速且可靠的循环伏安法、线性扫描伏安法、方波伏安法和差分脉冲伏安法,用于测定药物制剂中的依托度酸。所提出的方法基于依托度酸在含0.1 M高氯酸锂的乙腈溶液中于铂电极上的电化学氧化。在1.03 V处观察到明确的氧化峰。线性扫描伏安法、方波伏安法和差分脉冲伏安法中依托度酸的校准曲线在2.5 - 50 μg/ml浓度范围内分别呈线性。依托度酸的日内和日间精密度值均小于4.69,准确度(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,三种片剂辅料均未产生干扰。本研究中开发的方法准确、精密,可轻松应用于作为药物制剂的依托度酸片、他多拉克片和依托度因片。