Süslü I, Altinöz S
Department of Analytical Chemistry, Faculty of Pharmacy, Hacettepe University, Ankara, Turkey.
Pharmazie. 2008 Jun;63(6):428-33.
The electrochemical behavior of the antihypertensive drug quinapril was investigated at a hanging mercury drop electrode using different voltammetric techniques such as cyclic voltammetry, square-wave voltammetry and chronoamperometry. A simple and sensitive square-wave voltammetric method for the electrochemical analysis of quinapril in its pharmaceutical formulations was developed and validated. The experimental and instrumental parameters affecting the peak current of quinapril were investigated. Various buffers such as Britton Robinson, borate and phosphate buffers at different pH values (3.0-11.0) were examined as supporting electrolyte. The optimum conditions were obtained using Britton Robinson buffer at pH 10.0 and frequency: 50 Hz, scan increment: 4 mV and pulse amplitude: 25 mV. A well-defined peak current was observed at the hanging mercury drop electrode at -1100 mV vs. Ag/AgCl reference electrode. This proposed method was validated by evaluating linearity, sensitivity, repeatability, accuracy, precision, selectivity, recovery, robustness and ruggedness. The linear calibration range was 0.50-8.68 microg mL-' (r = 0.9992). The detection and quantification limits of this method were 0.22 and 0.50 Ctg mL(-1) and intra-day and inter-day precision were between 0.81-4.32% (n = 7), respectively. The developed method was applied successfully for the determination of quinapril in its tablet dosage forms. The average amount of quinapril in tablets was found as 20.26 +/- 0.12 with RSD of 1.60% for 20 mg tabletsand 40.55 +/- 0.23 with RSD of 1.52% for 40 mg tablets.
使用循环伏安法、方波伏安法和计时电流法等不同伏安技术,在悬汞滴电极上研究了抗高血压药物喹那普利的电化学行为。开发并验证了一种用于药物制剂中喹那普利电化学分析的简单灵敏的方波伏安法。研究了影响喹那普利峰电流的实验和仪器参数。考察了不同pH值(3.0 - 11.0)的各种缓冲液,如 Britton Robinson 缓冲液、硼酸盐缓冲液和磷酸盐缓冲液作为支持电解质。在pH 10.0的 Britton Robinson 缓冲液、频率为50 Hz、扫描增量为4 mV和脉冲幅度为25 mV的条件下获得了最佳条件。在相对于 Ag/AgCl 参比电极 - 1100 mV 处的悬汞滴电极上观察到一个明确的峰电流。通过评估线性、灵敏度、重复性、准确性、精密度、选择性、回收率、稳健性和耐用性对该方法进行了验证。线性校准范围为0.50 - 8.68 μg mL⁻¹(r = 0.9992)。该方法的检测限和定量限分别为0.22和0.50 μg mL⁻¹,日内和日间精密度分别在0.81 - 4.32%(n = 7)之间。所开发的方法成功应用于片剂剂型中喹那普利的测定。20 mg片剂中喹那普利的平均含量为20.26 ± 0.12,相对标准偏差为1.60%;40 mg片剂中喹那普利的平均含量为40.55 ± 0.23,相对标准偏差为1.52%。