...
首页> 外文期刊>Journal of Analytical Sciences, Methods and Instrumentation >A Comparative Evaluation of Polystyrene Divinylbenzene Copolymer HPLC Columns on the Chromatographic Performance of the Compendial Method for Doxycycline Hyclate Capsules: Implications for Method Implementation of a Medical Countermeasure Medication
【24h】

A Comparative Evaluation of Polystyrene Divinylbenzene Copolymer HPLC Columns on the Chromatographic Performance of the Compendial Method for Doxycycline Hyclate Capsules: Implications for Method Implementation of a Medical Countermeasure Medication

机译:聚苯乙烯二乙烯基苯共聚物HPLC色谱柱对盐酸多西环素胶囊方法的色谱性能的比较评估:对医学对策药物实施方法的启示

获取原文
           

摘要

The purpose of this study was to evaluate the impact of polystyrene divinylbenzene copolymer HPLC columns on the chromatographic performance of the USP compendial method for doxycycline hyclate. The compendial method was implemented based on the assessment of the chromatographic performance of six USP defined L21 polystyrene divinylbenzene HPLC columns. Modifications to the method were based on USP for chromatography. The method was validated for the determination of doxycycline hyclate and its impurities in commercially available drug products. A number of different polystyrene-divinylbenzene columns were tested and failed to provide selectivity for the resolution of doxycycline and its impurities. Separation was optimally achieved on an Agilent PLPR-S column (250 × 4.6 mm, 8 μm) by using an Agilent 1260 series HPLC system. Doxycycline hyclate and its impurities were eluted isocratically at a flow rate of 1 mL/min with mobile phase and detected at 270 nm. The column temperature was maintained at 60oC. The method was validated according to USP category I requirements for Assay. Validation acceptance criteria were met in all cases. The analytical range for doxycycline hyclate was 50 - 250 μg/mL and the linearity was r2 > 0.999 over three days. The method was determined to be specific. Both accuracy (95.1% - 102.4%) and precision (0.50% - 4.8%) were established across the analytical range for low, intermediate and high QC concentrations. Method applicability was demonstrated by analyzing marketed products of doxycycline hyclate, in which results showed potency meeting USP acceptance criteria. In conclusion, this study described the remarkable differences in selectivity that were encountered during the implementation phase for the compendial methods for doxycycline and its impurities in marketed products and it could be used in the future to assss the product quality of doxycycline hyclate capsules stored in the National stockpiles.
机译:本研究的目的是评估聚苯乙烯二乙烯基苯共聚物HPLC色谱柱对盐酸多西环素的USP药典方法的色谱性能的影响。该药典方法是根据对六种USP定义的L21聚苯乙烯二乙烯基苯HPLC色谱柱的色谱性能进行评估而实施的。对方法的修改基于色谱法的USP。该方法经验证可用于测定市售药品中的强力霉素和其杂质。测试了许多不同的聚苯乙烯-二乙烯基苯色谱柱,这些色谱柱无法为强力霉素及其杂质的分离提供选择性。通过使用Agilent 1260系列HPLC系统,在Agilent PLPR-S色谱柱(250×4.6 mm,8μm)上实现了最佳分离。用流动相以1 mL / min的流速等度洗脱盐酸多西环素及其杂质,并在270 nm处检测。柱温保持在60℃。该方法已根据USP I类分析要求进行了验证。在所有情况下都满足验证接受标准。盐酸多西环素的分析范围为50-250μg/ mL,三天线性度为r2> 0.999。确定该方法是特定的。在低,中和高QC浓度的整个分析范围内均建立了准确度(95.1 %-102.4 %)和精确度(0.50 %-4.8 %)。通过分析盐酸多西环素的市售产品证明了该方法的适用性,结果表明其效力符合USP接受标准。总之,本研究描述了在实施阶段,市售产品中强力霉素及其杂质的药典方法在选择性方面存在显着差异,并且该技术可在将来用于评估储存在药品中的强力霉素透明胶囊的产品质量。国家库存。

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