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国内外溶出度试验用标准片的研究及应用 被引量:15

Overview and application of reference standard tablets for dissolution tester qualification
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摘要 回顾了国内外溶出度试验用标准片的研究、建立情况及各种标准片的历史数据,介绍了我国水杨酸标准片的溶出特性,对溶出度标准片的作用及面临的挑战,以及国际上对溶出度标准片的观点进行了论述。 Overview the history of investigation,establishment of different kinds of reference standard tablets(granules) for dissolution tester's qualification,provides the historical data of reference standard tablets official dissolution range.Describe the characteristics of Chinese salicylic acid reference standard tablets,discuss the application and challenges of reference standard tablets,summarize the different perspective on reference standard tablets from industry,manufacturer and regulatory authority.
出处 《药物分析杂志》 CAS CSCD 北大核心 2012年第8期1509-1515,共7页 Chinese Journal of Pharmaceutical Analysis
基金 化学新药质量标准研究与评价技术平台2011ZX09303-001资助项目
关键词 溶出度 校正片 机械校正 化学校正 水杨酸标准片 泼尼松标准片 马来酸氯苯那敏缓释片 茶碱缓释颗粒 美国药典 欧洲药典 日本药典 中国药典 dissolution calibrator mechanical calibration chemical calibration salicylic acid tablets reference standard prednisone tablets reference standard chlorpheniramine maleate extended-release tablets reference standard theophylline extended-release beads reference standard United Sates Pharmacopoeia European Pharmacopoeia Japanese Pharmacopoeia Chinese Pharmacopoeia
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参考文献9

  • 1Data Sheet for USP Dissolution Calibrator,Non-disintegrating Type,for Apparatus Suitability Test,Salicylic Acid Tablets,Lot F,Approximately 300 mg.
  • 2The USP performance test and the dissolution procedure statement..http://www.usp.org/usp-nf/notices/usp-performance-test-and-dissolution-procedure-statement.
  • 3http://www.usp.org/reference-standards/use-and-storage/dissolution-pvt-ranges.
  • 4Certificate of USP prednisone tablets Lot P1I300..http://www.usp.org/pdf/EN/referenceStandards/certificates/1559505-P1I300.pdf.
  • 5ISO.ISO 5725-6:1994,Accuracy (Trueness and Precision) of Measurement Methods and Results-Part 6:Use in Practice of Accuracy Values.Geneva,Switzerland:ISO,1994.
  • 6Aiache JM,Aoyagi N,Blume H,et al.FIP,1997-Joint Report of the Section for Official Laboratories and Medicines Control Services and the Section of Industrial Pharmacists of the FIP,"FIP Guidelines for Dissolution Testing of Solid Oral Products".Dissolut Technol,1997,4(4):5.
  • 7Hamilton JF,Moore TW,Kerner CM.Reproducibility of Dissolution Test Results.Pharm Forum,1995,21:1383.
  • 8Oates M,Brune S,Gray V,et al.PhRMA Subcommittee on Dissolution calibration:dissolution calibrator:recommendations for reduced chemical testing and enhanced mechanical calibration.Pharm Forum,2000,26(4):1149.
  • 9Konieczny J,Cohen E,Thomas A,et al.Validation Technique of Dissolution Test for Control of Drug Quality and Bioequivalence,1980,Presented at the Interphex USA Technical Conference.

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