首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Simultaneous determination of atenolol, chlorthalidone and amiloride in pharmaceutical preparations by capillary zone electrophoresis with ultraviolet detection.
【24h】

Simultaneous determination of atenolol, chlorthalidone and amiloride in pharmaceutical preparations by capillary zone electrophoresis with ultraviolet detection.

机译:毛细管区带电泳-紫外检测法同时测定药物制剂中的阿替洛尔,氯噻酮和阿米洛利。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Capillary zone electrophoresis methods for the simultaneous determination of the beta-blocker drugs, atenolol, chlorthalidone and amiloride, in pharmaceutical formulations have been developed. The influences of several factors (buffer pH, concentration, applied voltage, capillary temperature and injection time) were studied. Using phenobarbital as internal standard, the analytes were all separated in less than 4 min. The separation was carried out in normal polarity mode at 25 degrees C, 25 kV and using hydrodynamic injection (10 s). The separation was effected in an uncoated fused-silica capillary (75 mum i.d. x 52 cm) and a background electrolyte of 25 mm H(3)PO(4) adjusted with 1 m NaOH solution (pH 9.0) and detection at 198 nm. The method was validated with respect to linearity, limit of detection and quantification, accuracy, precision and selectivity. Calibration curves were linear over the range 1-250 microg/mL for atenolol and chlorthalidone and from 2.5-250 microg/mL for amiloride. The relative standard deviations of intra- and inter-day migration times and corrected peak areas were less than 6.0%. The method showed good precision and accuracy and was successfully applied to the simultaneous determination of atenolol, chlorthalidone and amiloride in various pharmaceutical tablets formulations.
机译:已经开发出用于同时测定药物制剂中β受体阻滞剂,阿替洛尔,氯噻酮和阿米洛利的毛细管区带电泳方法。研究了几个因素的影响(缓冲液pH,浓度,施加电压,毛细管温度和进样时间)。使用苯巴比妥作为内标,所有分析物在不到4分钟的时间内被分离。分离是在25摄氏度,25 kV的正常极性模式下,并使用流体动力注入(10 s)进行的。分离是在未涂覆的熔融石英毛细管(内径75毫米x 52厘米)和25毫米H(3)PO(4)的背景电解质中进行的,并用1 m NaOH溶液(pH 9.0)调节并在198 nm处检测。该方法在线性,检测和定量限,准确性,精密度和选择性方面得到了验证。阿替洛尔和氯噻酮的校准曲线在1-250 microg / mL范围内线性,阿米洛利的校准曲线在2.5-250 microg / mL范围内。日内和日间迁移时间以及校正后的峰面积的相对标准偏差小于6.0%。该方法具有良好的精密度和准确性,已成功用于多种药物片剂中阿替洛尔,氯噻酮和阿米洛利的同时测定。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号