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同时发生降解的药物片剂溶解的浓度曲线

Concentration profile for the dissolution of drug tablets undergoing simultaneous degradation.

作者信息

Chen H S, Chang S Y, Evans T L, Gross J F

出版信息

J Pharmacokinet Biopharm. 1980 Dec;8(6):621-31. doi: 10.1007/BF01060057.

DOI:10.1007/BF01060057
PMID:7229912
Abstract

An empirical approach to the concentration-time history of a dissolving drug has resulted in a cube-root equation in which the characteristic constant of the equation embodies the important physical variables of the system. This expression has been used to study the dissolution of a drug that degrades simultaneously in the test solution. An alternative representation of the dissolution process is first-order kinetics. These two approaches are compared by fitting the experimental data of the dissolution of digoxin and melphalan tablets in various media, and a new method for the proper analysis of data for the dissolution of tablets that simultaneously degrade in the test solution is presented.

摘要

一种针对溶解药物浓度-时间历程的经验方法得出了一个立方根方程,该方程的特征常数体现了系统的重要物理变量。此表达式已用于研究在测试溶液中同时降解的药物的溶解情况。溶解过程的另一种表示形式是一级动力学。通过拟合地高辛和美法仑片剂在各种介质中的溶解实验数据,对这两种方法进行了比较,并提出了一种对在测试溶液中同时降解的片剂溶解数据进行适当分析的新方法。

相似文献

1
Concentration profile for the dissolution of drug tablets undergoing simultaneous degradation.同时发生降解的药物片剂溶解的浓度曲线
J Pharmacokinet Biopharm. 1980 Dec;8(6):621-31. doi: 10.1007/BF01060057.
2
Testing lyoequivalency for three commercially sustained-release tablets containing diltiazem hydrochloride.对三种市售盐酸地尔硫卓缓释片进行溶出度等效性测试。
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Disintegration-dissolution analysis of percent dissolved-time data.溶解百分比-时间数据的崩解-溶解分析
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6
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Digoxin degradation in acidic dissolution medium.地高辛在酸性溶解介质中的降解
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本文引用的文献

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Interpretation of percent dissolved-time plots derived from in vitro testing of conventional tablets and capsules.源自传统片剂和胶囊体外测试的溶解时间百分比图的解读。
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Absorption of orally given digoxin preparations.口服地高辛制剂的吸收情况。
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Nicotine base permeation through silicone elastomers: comparison of dimethylpolysiloxane and trifluoropropylmethylpolysiloxane systems.尼古丁碱透过硅氧烷弹性体的研究:二甲基聚硅氧烷与三氟丙基甲基聚硅氧烷体系的比较
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5
Linearization of dissolution rate curves by the Weibull distribution.用威布尔分布对溶出速率曲线进行线性化处理。
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6
Simple transformation method for predicting plasma drug profiles from dissolution rates.基于溶出速率预测血浆药物浓度曲线的简易转换方法。
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Intersubject variation in absorption of digoxin in normal volunteers.
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Use of in vitro dissolution data to predict plasma drug profiles.利用体外溶出数据预测血浆药物浓度曲线。
J Pharm Sci. 1977 Sep;66(9):1359-62. doi: 10.1002/jps.2600660948.
10
Bioavailability of drugs: the digoxin dilemma.药物的生物利用度:地高辛的困境。
Clin Pharmacokinet. 1976;1(1):36-51. doi: 10.2165/00003088-197601010-00004.