首页> 外文期刊>Drug testing and analysis >Application of ion-pair complexation reaction for the spectrophotometric determination of bupropion hydrochloride in pharmaceuticals
【24h】

Application of ion-pair complexation reaction for the spectrophotometric determination of bupropion hydrochloride in pharmaceuticals

机译:离子对络合反应光度法测定药物中盐酸安非他酮的应用

获取原文
获取原文并翻译 | 示例
       

摘要

This is the first report on the use of visible spectrophotometry for the determination of bupropion hydrochloride (BUPH), a second-generation antidepressant, in pharmaceuticals. Two sensitive, selective, and cost-effective spectrophotometric methods are described. The first method (method A) is based on the formation of yellow-coloured ion-pair complex between the BUPH and methyl orange (MO) at pH 3.80 ± 0.10 which was extracted into dichloromethane and the absorbance measured at 425 nm. The second method (method B) is based on the breaking of the yellow BUPH-MO ion-pair complex in acid medium followed by the measurement of the red-pink colour at 520 nm. Beer's Law is obeyed over the concentration ranges of 1.00-12.0 and 0.48-7.20 μg ml -1 BUPH for method A and method B, respectively. The molar absorptivities are calculated to be 2.18 × 10 4 and 3.79 × 10 4 l mol -1 cm -1 for method A and method B, respectively, and the corresponding Sandell sensitivity values are 0.0127 and 0.0073 μg cm -2. The limits of detection and quantification have also been reported. The proposed methods were applied successfully to the determination of BUPH in pure drug and commercial tablets. The accuracy and reliability of the proposed methods were further ascertained by recovery studies via standard addition technique.
机译:这是有关使用可见分光光度法测定药物中第二代抗抑郁药安非他酮盐酸盐(BUPH)的第一份报告。描述了两种灵敏,选择性和成本效益高的分光光度法。第一种方法(方法A)是基于BUPH和甲基橙(MO)在pH 3.80±0.10下形成黄色的离子对络合物,然后将其萃取到二氯甲烷中并在425 nm下测量吸光度。第二种方法(方法B)基于酸性介质中黄色BUPH-MO离子对络合物的断裂,然后在520 nm处测量红粉红色。方法A和方法B分别在1.00-12.0和0.48-7.20μgml -1 BUPH的浓度范围内遵守比尔定律。方法A和方法B的摩尔吸光度分别计算为2.18×10 4和3.79×10 4 l mol -1 cm -1,相应的Sandell灵敏度值为0.0127和0.0073μgcm -2。还已经报道了检测和定量的极限。所提出的方法已成功应用于纯药物和市售片剂中BUPH的测定。通过标准添加技术的回收率研究进一步确定了所提出方法的准确性和可靠性。

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