首页> 外文期刊>International Journal of Pharmaceutical Sciences and Research >SIMPLE AND RAPID SPECTROPHOTOMETRIC DETERMINATION OF ATENOLOL AND ESMOLOL β-BLOCKERS IN PHARMACEUTICAL FORMULATIONS AND SPIKED WATER SAMPLES
【24h】

SIMPLE AND RAPID SPECTROPHOTOMETRIC DETERMINATION OF ATENOLOL AND ESMOLOL β-BLOCKERS IN PHARMACEUTICAL FORMULATIONS AND SPIKED WATER SAMPLES

机译:简便快速的分光光度法测定药物配方和加味水样中的阿替洛尔和艾司洛尔β阻滞剂

获取原文
           

摘要

Atenolol and esmolol drugs belonging to a β–blocker group are frequently used for the treatment of cardiovascular diseases. These drugs are also charged as water pollutants. A new simple and rapid spectro-photometric method has been developed for their determination in pharmaceutical formulations and in spiked water samples. The proposed method is based on the derivatization of the amino function present in these drugs to the corresponding yellow copper (I) drug dithiocarbamate derivative through reaction with carbon disulphide, pyridine and copper (I) perchlorate in aqueous acetonitrile. The analysis is accomplished for their determination in pharmaceutical formulations by measuring absorbance at 425 nm for atenolol and 420 nm for esmolol. For the determination of these drugs in spiked water samples, the coloured complex is extracted into chloroform and the absorbance of the chloroform extracts is measured at 415 nm and 410 nm for atenolol and esmolol respectively. Linear correlation is obtained in the range 1.00 – 22.00 and 1.50 – 25.00 μg mL-1 with detection limits of 0.10 and 0.15μg mL-1 for atenolol and esmolol respectively. The proposed methods show good recoveries of atenolol and esmolol from pharmaceutical formulations and spiked water samples and are in the ranges from 99.00 -100.40% and 98.20 – 100.80% respectively. The 1:1 stoichiometry of the colour reaction between drug as dithiocarbamate derivative and copper (I) perchlorate has been established by photometric titrations. The latter also provides an alternative method for the determination of above drugs in pharmaceutical formulations.
机译:属于β受体阻滞剂的阿替洛尔和艾司洛尔药物经常用于治疗心血管疾病。这些药物也被列为水污染物。已经开发出一种新的简单而快速的分光光度法,用于测定药物制剂和加标水样品中的含量。所提出的方法基于在乙腈水溶液中与二硫化碳,吡啶和高氯酸铜(I)反应,将这些药物中存在的氨基官能团衍生为相应的黄色铜(I)药物二硫代氨基甲酸酯衍生物。通过测定阿替洛尔在425 nm和艾司洛尔在420 nm的吸光度来完成对它们在药物制剂中的测定分析。为了测定加标水样品中的这些药物,将有色配合物萃取到氯仿中,并分别在415 nm和410 nm下测量氯仿提取物对阿替洛尔和艾司洛尔的吸光度。线性相关性在1.00 – 22.00和1.50 – 25.00μgmL -1 范围内获得,阿替洛尔和艾司洛尔的检出限分别为0.10和0.15μgmL -1 。所提出的方法显示出从药物制剂和加标水样中获得的阿替洛尔和艾司洛尔的良好回收率,分别在99.00 -100.40%和98.20 – 100.80%的范围内。通过光度滴定已经建立了药物二硫代氨基甲酸酯衍生物与高氯酸铜(I)之间颜色反应的1:1化学计量。后者还提供了测定药物制剂中上述药物的替代方法。

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