...
首页> 外文期刊>Journal of AOAC International >Development and Validation of a Stability-Indicating HPLC-Photodiode Array Detector Method for Formulation Analysis and Degradation Kinetics and Dissolution Studies of Mycophenolate Sodium and HPLC/MS/MS Characterization of its Stress Degradation Products
【24h】

Development and Validation of a Stability-Indicating HPLC-Photodiode Array Detector Method for Formulation Analysis and Degradation Kinetics and Dissolution Studies of Mycophenolate Sodium and HPLC/MS/MS Characterization of its Stress Degradation Products

机译:用于霉酚酸酯钠的配方分析和降解动力学及溶解研究的稳定性指示HPLC-光电二极管阵列检测器方法的开发和验证,以及应力降解产物的HPLC / MS / MS表征

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

A simple stability-indicating isocratic RP-HPLC method was developed and validated for the determination of mycophenolate sodium and its alkali degradation product. Forced degradation of the drug was carried out under thermolytic, photolytic, acid/base hydrolytic, and oxidative stress conditions. Alkali degradation product DP1 was isolated, and separation of stress degradation products was achieved on a Symmetry C18 (250 x 4.6 mm x 5.0 pm) column using the mobile phase methanol-acetate buffer adjusted with acetic acid to pH 6.0 (76 + 24, v/v) at a 0.55 mL/min flow rate and 50°C. Data were integrated at the detection wavelength of 251 nm. The method validation characteristics included accuracy, precision, linearity, range, specificity, and sensitivity per International Conference on Harmonization guidelines. Robustness testing was conducted to evaluate the effect of minor changes in the chromatographic conditions and to establish appropriate system suitability parameters. Structural elucidation ofdegraded products was performed by HPLC/MS/MS. The method was used successfully for drug product analysis, dissolution study, and determination of the drug's acid, alkali, and oxidative degradation kinetics.
机译:建立了指示稳定性的等度简单RP-HPLC方法,该方法可用于测定麦考酚酸钠及其碱降解产物。在热解,光解,酸/碱水解和氧化应激条件下进行药物的强制降解。分离出碱降解产物DP1,并使用Symmetric C18(250 x 4.6 mm x 5.0 pm)色谱柱,使用乙酸调至pH 6.0的流动相甲醇-乙酸盐缓冲液,实现了应力降解产物的分离(76 + 24,v / v),流速为0.55 mL / min,温度为50°C。在251nm的检测波长下对数据进行积分。根据国际协调会议指南,方法验证特征包括准确性,精密度,线性,范围,特异性和敏感性。进行了稳健性测试,以评估色谱条件微小变化的影响并建立适当的系统适用性参数。通过HPLC / MS / MS进行降解产物的结构阐明。该方法已成功用于药物产品分析,溶出度研究以及药物的酸,碱和氧化降解动力学的测定。

著录项

相似文献

  • 外文文献
  • 中文文献
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