首页> 外文期刊>药物分析学报:英文版 >Identification, synthesis and characterization of process related impurities of benidipine hydrochloride, stress-testingstability studies and HPLC/UPLC method validations
【24h】

Identification, synthesis and characterization of process related impurities of benidipine hydrochloride, stress-testingstability studies and HPLC/UPLC method validations

机译:盐酸贝尼地平的工艺相关杂质的鉴定,合成和表征,应力测试稳定性研究和HPLC / UPLC方法验证

获取原文
获取原文并翻译 | 示例
       

摘要

Benidipine hydrochloride, used as an antihypertensive agent and long-acting calcium antagonist, is synthesized for commercial use as a drug substance in highly pure form. During the synthetic process development studies of benidipine, process related impurities were detected. These impurities were identi fi ed, synthesized and characterized and mechanisms of their formation were discussed in detail.After all standardization procedures, they were used as reference standards for analytical studies. In addition, a separate HPLC method was developed and validated for detection of residual 1-benzylpiperidin-3-ol(Ben-2), which is used during benidipine synthesis and controlled as a potential process related impurity. As complementary of this work, stress-testing studies of benidipine were carried out under speci fi ed conditions and a stability-indicating UPLC assay method was developed, validated and used during stability studies of benidipine.

著录项

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