首页> 外文期刊>Indian drugs >QUANTITATIVE DETERMINATION OF DEFERASIROX IN BULK AND PHARMACEUTICAL FORMULATION BY UV SPECTROPHOTOMETRIC METHOD
【24h】

QUANTITATIVE DETERMINATION OF DEFERASIROX IN BULK AND PHARMACEUTICAL FORMULATION BY UV SPECTROPHOTOMETRIC METHOD

机译:紫外分光光度法定量测定散装中的去铁含量及制药配方。

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

A simple, fast and reliable zero order spectrophotometric method was developed for determination of deferasirox in bulk and pharmaceutical dosage forms. Beer's law was obeyed in concentration range of 2-12 u/mL deferasirox at 245.6 nm wavelength. The correlation coefficient was found to be (r2 = 0.999), precision (repeatability % RSD 1.29), percentage recovery 100.054±0.271. The detection limit (DL) and quantitation limit (QL) were 0.247 ug/mL and 0.75 ug/mL respectively. The proposed method was found to be simple, accurate, precise, reproducible and gave an acceptable recovery of the analyte, which could be directly and easily applied to analysis of bulk and pharmaceutical tablet formulations of deferasirox.
机译:开发了一种简单,快速和可靠的零级分光光度法,用于测定散装和药物剂型中的地拉罗司。在245.6 nm波长下,在2-12 u / mL地拉罗司的浓度范围内遵守比尔定律。发现相关系数为(r2 = 0.999),精度(重复性%RSD 1.29),回收率100.054±0.271。检出限(DL)和定量限(QL)分别为0.247 ug / mL和0.75 ug / mL。发现所提出的方法简单,准确,精确,可重现,并提供了可接受的分析物回收率,可以直接,轻松地将其用于地拉罗司的散装和药物片剂分析。

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