Abdelal A A, Kitagawa S, Ohtani H, El-Enany N, Belal F, Walash M I
Department of Materials Science and Engineering, Graduate School of Engineering, Nagoya Institute of Technology, Gokiso, Showa, Nagoya 466-8555, Japan.
J Pharm Biomed Anal. 2008 Feb 13;46(3):491-7. doi: 10.1016/j.jpba.2007.11.012. Epub 2007 Nov 21.
Rapid and simple capillary electrophoresis (CE) methods were developed for the simultaneous determinations of cinnarizine and domperidone (CN/DOM) and cinnarizine and nicergoline (CN/NIC) in their co-formulated tablets. The optimized CE conditions were as follows: running buffer, methanol-acetate buffer (pH 3.0, 10 mM) (80:20 and 85:15 (v/v) for CN/DOM and CN/NIC, respectively); applied voltage, 20 kV; UV detection wavelengths, 215 and 227 nm for CN/DOM and CN/NIC, respectively; hydrodynamic injection was performed at a height of 25 mm for 30 s. Quinine hydrochloride and nicardipine hydrochloride were used as internal standards for the determination of CN/DOM and CN/NIC, respectively. Calibration curves were linear over the ranges 0.25-20/0.375-15 microg/ml (CN/DOM) and 0.25-25/0.4-10 microg/ml (CN/NIC) in each optimized condition. Detection limits were 0.074/0.119 microg/ml and 0.072/0.116 microg/ml for CN/DOM and CN/NIC, respectively. The proposed methods were successfully applied for the simultaneous determination of both CN/DOM and CN/NIC in their co-formulated tablets without interfering peaks due to the excipients present in the pharmaceutical tablets. The estimated amounts of CN/DOM and CN/NIC were almost identical with the certified values, and their percentage relative standard deviation values (%R.S.D.) were found to be < or =2.34% (n=3).
开发了快速简便的毛细管电泳(CE)方法,用于同时测定复方片剂中桂利嗪与多潘立酮(CN/DOM)以及桂利嗪与尼麦角林(CN/NIC)的含量。优化后的CE条件如下:运行缓冲液,甲醇 - 醋酸盐缓冲液(pH 3.0,10 mM)(CN/DOM和CN/NIC分别为80:20和85:15(v/v));施加电压,20 kV;紫外检测波长,CN/DOM和CN/NIC分别为215和227 nm;在25 mm高度进行30 s的流体动力学进样。分别使用盐酸奎宁和盐酸尼卡地平作为测定CN/DOM和CN/NIC的内标。在每个优化条件下,校准曲线在0.25 - 20/0.375 - 15 μg/ml(CN/DOM)和0.25 - 25/0.4 - 10 μg/ml(CN/NIC)范围内呈线性。CN/DOM和CN/NIC检测限分别为0.074/0.119 μg/ml和0.072/0.116 μg/ml。所提出的方法成功应用于同时测定复方片剂中的CN/DOM和CN/NIC,由于药物片剂中的辅料没有干扰峰。CN/DOM和CN/NIC的估计量与认证值几乎相同,其相对标准偏差百分比值(%R.S.D.)<或=2.34%(n = 3)。