首页> 外文期刊>Journal of liquid chromatography and related technologies >Simple and fast rp-hplc method for the determination of prednisolone sodium phosphate, prednisolone, atropine, and homatropine as residuals in cleaning validation of industrial pharmaceutical equipment
【24h】

Simple and fast rp-hplc method for the determination of prednisolone sodium phosphate, prednisolone, atropine, and homatropine as residuals in cleaning validation of industrial pharmaceutical equipment

机译:简单快速的rp-hplc方法测定工业制药设备清洁验证中的泼尼松龙磷酸钠,泼尼松龙,阿托品和奥马托品残留量

获取原文
获取原文并翻译 | 示例
       

摘要

Determining traces of pharmaceuticals in equipment is an important step for controlling cross-contamination during the production cycle. Time-consuming analysis is not applicable because it of incremental costs, especially in evaluating residuals as steroids and alkaloids that require a fast and specific technique. Here, an isocratic reversed-phase HPLC method was developed for the trace analysis of Prednisolone Sodium Phosphate (PSP), Homatropine (HOM), Atropine (ATR), and Prednisolone (PRE) in cleaning samples from pharmaceutical equipment. For this, a mobile phase mixture of 35/65 (V/V) acetonitrile/ potassium dibasic phosphate 10 m mol L-1, pH 6.9 at 1.0 mL min -1, with a phenyl-hexyl column, were used. These parameters enabled quantifying the analytes within 7.0 min, detecting ATR and HOM at 210 nm, while PSP and PRE were monitored at 240 nm, being lineal between 1-100 μg mL -1 in all cases. The quantification and detection limits were 0.04 and 0.02 μg mL-1 for PSP, ATR, and HOM and 0.02 and 0.01 μg mL-1 for PRE. The method proved its worth and specificity even in presence of other formulation components of the final dosage forms without extraction or concentration procedures.
机译:确定设备中药物的含量是控制生产周期中交叉污染的重要步骤。耗时的分析不适用,因为它会增加成本,尤其是在评估残留物(需要快速和特定技术的类固醇和生物碱)中。在此,开发了一种等度反相HPLC方法,用于从制药设备中清洗样品中的泼尼松龙磷酸钠(PSP),霍马曲平(HOM),阿托品(ATR)和泼尼松龙(PRE)的痕量分析。为此,使用了带有苯基己基柱的流动相混合物,该流动相混合物为10 m mol L-1的35/65(V / V)乙腈/磷酸二氢钾,pH 6.9,1.0 mL min -1。这些参数能够在7.0分钟内对分析物进行定量,在210 nm处检测ATR和HOM,而在240 nm处监测PSP和PRE,在所有情况下均为1-100μgmL -1之间。 PSP,ATR和HOM的定量和检出限分别为0.04和0.02μgmL-1,PRE为0.02和0.01μgmL-1。该方法即使在没有提取或浓缩程序的最终剂型的其他制剂成分存在下也证明了其价值和特异性。

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