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Improvement of release criteria for immediate release solid oral dosage forms.

机译:改善速释固体口服剂型的释放标准。

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摘要

Herewith are presented the results of an investigation the statistical power of USP compendial release tests and recommended alternatives.;The U.S. drug supply chain, formerly protected by a closed distribution network, is now threatened by the legal and illegal importation of drug products. Whereas quality can never be inspected into final products, compendial release standards may represent the only valid assessment that products of dubious origin would receive. Reliable tests for content uniformity and dissolution are required to protect the safety of the supply chain. A study was designed to test the hypothesis that existing compendial tests for content uniformity and dissolution would protect the supply chain against substandard and counterfeit drugs if basic field tests failed.;Compendial tests for content uniformity and dissolution were evaluated for statistical power using simulation studies. The results revealed that the revised content uniformity test, based on tolerance analysis, was subject to an unacceptable level of consumers' risk. The Bergum method proved to be an excellent secondary standard for product assessment and is recommended as an alternative to the USP method.;Simulations with the USP dissolution test revealed significant weaknesses and inconsistencies in the test structure. Theoretical models and power assessments confirmed that the coverage specification of the dissolution test was an unacceptably high 50% coverage with 50% confidence.;A Bayesian D-optimal design program was used to investigate alternative methods to improve the coverage capability of the USP dissolution test. The result of this program was the identification of two alternatives to the existing USP procedure. The first alternative is based on the addition of attribute coverage tests to stages 2 and 3 of the USP test, whereas the second alternative is based on the concept of tolerance analysis.;Validation studies confirmed that both alternatives significantly improved the statistical power of the USP dissolution test without increasing the sample size or modifying the current three-stage procedure. The attribute test is non-parametric and behaves similarly to the existing USP with improved coverage, whereas the continuous alternative is more sensitive and is consistent with the recent revisions to the content uniformity test.
机译:特此介绍调查结果,以了解USP药典释放测试的统计能力和建议的替代方法;美国药品供应链原先受到封闭的分销网络的保护,现在受到合法和非法进口药品的威胁。尽管永远无法检查最终产品的质量,但药典发布标准可能是可疑来源产品唯一能接受的有效评估。为了保证供应链的安全,需要对含量均匀性和溶出度进行可靠的测试。设计一项研究来检验以下假设:如果基本现场测试失败,则现有的含量均一性和溶解度药典测试将保护供应链免受不合格和假药的侵害;使用模拟研究评估了含量均一性和溶出度药典测试的统计功效。结果显示,基于容忍度分析的修订后的内容均一性测试受到消费者风险水平的不可接受的影响。事实证明,Bergum方法是产品评估的极好的次要标准,建议替代USP方法。; USP溶出度测试的模拟显示测试结构存在明显的弱点和不一致之处。理论模型和功率评估证实,溶出度测试的覆盖范围指标是50%的置信度,令人难以接受,而置信度为50%。;贝叶斯D最优设计程序用于研究替代方法以提高USP溶出度测试的覆盖范围。该计划的结果是确定了现有USP程序的两个替代方案。第一种选择是基于在USP测试的第2阶段和第3阶段增加了属性覆盖率测试,而第二种选择是基于公差分析的概念。验证研究证实,这两种选择都可以显着提高USP的统计能力溶出度测试,无需增加样品量或修改当前的三阶段程序。属性测试是非参数的,其行为与现有USP相似,但覆盖范围有所改善,而连续替代方法则更为敏感,并且与内容统一性测试的最新修订版一致。

著录项

  • 作者

    Lunney, Phillip Douglas.;

  • 作者单位

    Duquesne University.;

  • 授予单位 Duquesne University.;
  • 学科 Health Sciences Pharmacy.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 295 p.
  • 总页数 295
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:43:48

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