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    题名: 藥劑溶離率比對方法之應用與研究
    The Application and Research of Comparative in-Vitro Dissolution Data
    作者: 廖淑真
    Liaw, Shu-Jean
    贡献者: 林慧
    Lin, Huey
    廖淑真
    Liaw, Shu-Jean
    关键词: 溶離度試驗
    體外溶離
    體內生體相等
    Dissolution testing
    Inin-vitro dissolution
    In-vivo bioequivalence
    日期: 1996
    上传时间: 2016-04-28 11:48:27 (UTC+8)
    摘要: 目前在國內外藥界對比對溶離資料之處理方法有很多種.在本文以常用之二維隨機集區實驗設計,共變異數分析法,單變量分裂區集變異析法,Chow(1995)所提出之時間數列分析法,及美國食品藥物管理局在1995年11月所提出的方法,比較此五種方法並以電腦模擬不同情形之資料再對其結果予以分析.
    There are various ways of comparing dissolution profiles between two drug products. In this thesis, we compare five statistical methods often used,namely, two-way randomized block design, analysis of covariance, split-plot,time-series analysis method proposed by Chow (1995), and the method proposed by Food and Drug Administration (FDA) in November, 1995. The five methods are compared via simulation studies under different conditions, analyses arealso provided.
    參考文獻: 行政院衛生署科技研究發展計畫成果報告，「溶離率試驗比對基準之探討」，台北醫學院，民國八十四年.
    吳柏林，「時間數列分析導論」，華泰，民國八十四年.
    許興智、陳甘霖、陳朝洋，「藥劑的安定性及配方的篩選」，華榮，民國八十年.
    Chow, S. C., (1995). Statistical comparison between dissolution profiles of drug products. Submitted to J of Biopharm.
    Cochran, w. G., (1957). Analysis of covariance: its nature and uses. Biometrics, Vol. 13, No.3, 261-281.
    Duncan, A. l, (1974). Quality Control and Industrial Statistics, 4th edition. Richard D. Irwin, Inc. Homewood, III.
    FDA, (1995). Guidance for Industry Immediate Release Solid Oral Dosage Forms Scale-Up and Postapproval Changes: Chemistry, Manufacturing, and Controls, In-Vitro Dissolution Testing, and In-Vivo Bioequivalence Documentation, Food and Drug Administration, Rockville, Mayrland.
    Federer, W. T., (1957). Variance and covariance analysis for unbalanced cIassifications. Biometrics, Vol. 13, No.3, 333-362.
    Gill, J. L., (1988). Repeated measurement: split-plot trend analysis versus analysis of first differences. Biometrics, 44, 289-297.
    Mauger, J. W., Chilko, D., Howard, S., (1986). On the analysis of dissolution data. Drug Development and Industrial Pharmacy, 12(7), 969-992.
    Minitab, Minitab Inc. ,. State College Pennsylvania, USA, (1993).
    Montgomery, D. c., (1991). Design and Analysis of Experiments, 3rd edition. John Wiley and Sons, Inc. New York.
    Ronald D. Snee, (1972). On the analysis of response curve data. Technometrics,14(1), 47-62.
    Tsong, Y. and Hammerstrom, T. (1992). Statistical issues in drug quality control based on dissolution testing. Proceedings the Biopharmaceutical Section of the American Statistical Association, 295-300.
    描述: 碩士
    國立政治大學
    統計學系
    83354003
    資料來源: http://thesis.lib.nccu.edu.tw/record/#B2002002787
    数据类型: thesis
    显示于类别:[統計學系] 學位論文

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