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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Method development and validation for the simultaneous determination of cinnarizine and co-formulated drugs in pharmaceutical preparations by capillary electrophoresis.
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Method development and validation for the simultaneous determination of cinnarizine and co-formulated drugs in pharmaceutical preparations by capillary electrophoresis.

机译:通过毛细管电泳同时测定药物制剂中的肉桂利嗪和共同配制药物的方法开发和验证。

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摘要

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).
机译:建立了快速简便的毛细管电泳(CE)方法,用于同时测定共同配制的片剂中的桂利嗪和多潘立酮(CN / DOM)以及桂利嗪和尼麦角林(CN / NIC)。优化的CE条件如下:运行缓冲液,乙酸甲醇缓冲液(pH 3.0,10 mM)(对于CN / DOM和CN / NIC,分别为80:20和85:15(v / v));施加电压20 kV; CN / DOM和CN / NIC的紫外线检测波长分别为215和227 nm;在25 mm的高度进行30 s的流体动力注射。盐酸奎宁和盐酸尼卡地平分别用作测定CN / DOM和CN / NIC的内标。在每种优化条件下,校准曲线在0.25-20 / 0.375-15微克/毫升(CN / DOM)和0.25-25 / 0.4-10微克/毫升(CN / NIC)的范围内呈线性。 CN / DOM和CN / NIC的检出限分别为0.074 / 0.119 microg / ml和0.072 / 0.116 microg / ml。所提出的方法已成功地用于同时测定其共配制片剂中的CN / DOM和CN / NIC,而不会由于药物片剂中存在的赋形剂而干扰峰。 CN / DOM和CN / NIC的估计数量与认证值几乎相同,并且发现它们的相对标准偏差百分比(%R.S.D。)为<或= 2.34%(n = 3)。

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