...
首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Spectrophotometric determination of dapsone in pharmaceutical products using sodium 1,2-naphthoquinone-4-sulfonic as the chromogenic reagent
【24h】

Spectrophotometric determination of dapsone in pharmaceutical products using sodium 1,2-naphthoquinone-4-sulfonic as the chromogenic reagent

机译:1,2-萘醌-4-磺酸钠为显色剂分光光度法测定药品中氨苯砜的含量

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Spectrophotometric determination of dapsone is described. The dapsone reacts with sodium 1,2-naphthoquinone-4-sulfonic in pH 6.98 buffer solution to form a salmon pink compound, and its maximum absorption wavelength is at 525 nm, 6525 = 3.68 x 10(4) l mol(-1) cm(-1). The absorbance of dapsone from 0.40 to 10 mug ml(-1) obeys Beer's law. The linear regression equation of the calibration graph is C = 0.2334A + 0.01288, with a linear regression correlation coefficient of 0.9998, the detection limit is 0.24 mug ml(-1), and recovery is from 99.2 to 102.4%. Effects of pH, surfactant, organic solvents, foreign ions, and standing time on the determination of dapsone have been examined. This method is simple and can be used for the determination of dapsone in injection solution of dapsone. The results obtained by this method agreed with those by the official method (dead-stop titration method [The Chinese Pharmacopoeia, Pharmacopoeia Commission, Ministry of Health, vol. 2, fifth ed., PRC Chemical Industry Press, Beijing, 2000, p.720]). (C) 2004 Elsevier B.V. All rights reserved.
机译:描述了氨苯砜的分光光度测定。氨苯砜在pH 6.98缓冲溶液中与1,2-萘醌-4-磺酸钠反应形成鲑鱼粉红色化合物,其最大吸收波长为525 nm,6525 = 3.68 x 10(4)l mol(-1)厘米(-1)。氨苯砜的吸光度从0.40到10毫升(-1),符合比尔定律。校正图的线性回归方程为C = 0.2334A + 0.01288,线性回归相关系数为0.9998,检出限为0.24马克杯ml(-1),回收率为99.2至102.4%。研究了pH,表面活性剂,有机溶剂,外来离子和放置时间对氨苯砜测定的影响。该方法简便易行,可用于氨苯砜注射液中氨苯砜的测定。通过该方法获得的结果与通过官方方法(死点滴定法[中国药典,卫生部药典委员会,第2卷,第五版,中华人民共和国化学工业出版社,北京,2000年,第135页)一致。 720])。 (C)2004 Elsevier B.V.保留所有权利。

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