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Gauge repeatability and reproducibility for accessing variability during dissolution testing: A technical note

机译:量表可重复性和再现性,用于溶出度测试中的变异性:技术说明

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摘要

In this study, the gauge R&R method was used to analyze sources of variability for the paddle apparatus (USP apparatus 2). An initial evaluation of gauge R&R dissolution testing results using the amount dissolved at 30 minutes for a 10-mg prednisone tablet showed no instrument or operator contributions to variability but did highlight some vessel differences within an instrument. Based on this finding, a new mechanical calibration step was developed to improve the performance of the measurement system.
机译:在这项研究中,量规R&R方法用于分析桨式设备(USP设备2)的可变性来源。使用10 mg泼尼松片在30分钟时的溶解量对量具的R&R溶出度测试结果进行初步评估,结果表明仪器或操作者对变异性没有贡献,但确实突出了仪器中的某些血管差异。基于此发现,开发了新的机械校准步骤以改善测量系统的性能。

著录项

  • 来源
    《AAPS PharmSciTech》 |2007年第4期|11-15|共5页
  • 作者单位

    Food and Drug Administration Center for Drug Evaluation and Research Division of Pharmaceutical Analysis 63101 St Louis MO;

    Food and Drug Administration Center for Drug Evaluation and Research Division of Pharmaceutical Analysis 63101 St Louis MO;

    Food and Drug Administration Center for Drug Evaluation and Research Division of Pharmaceutical Analysis 63101 St Louis MO;

    Food and Drug Administration Center for Drug Evaluation and Research Division of Pharmaceutical Analysis 63101 St Louis MO;

    Food and Drug Administration Center for Drug Evaluation and Research Division of Pharmaceutical Analysis 63101 St Louis MO;

    Food and Drug Administration Center for Drug Evaluation and Research Division of Pharmaceutical Analysis 63101 St Louis MO;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Dissolution test; gauge RR; variability;

    机译:溶出度测试规程R&R变异性;

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