Drug absorption in the human body depends on the dissolution rate of the drug. Suitable dissolution characteristics are important to ensure that the drug will achieve the desired therapeutic effects. To assess the similarity of dissolution rates of several drug lots, we apply a general growth curve
Versatile kinetic approach to analysis of dissolution data
โ Scribed by Peter Veng Pedersen; James W. Myrick
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 662 KB
- Volume
- 67
- Category
- Article
- ISSN
- 0022-3549
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โฆ Synopsis
A new kinetically based dissolution equation is presented that considers dissolution of polydisperse systems and disintegrating solid dosage forms. The equation is applicable under sink as well as nonsink conditions and enables the specific dissolution rate parameter, the dispersion parameter, the disintegration lag time, and a newly introduced parameter, the dissolution availability, to be evaluated simultaneously and directly from percent of label claim dissolved versus time data. The equation showed excellent fit to dissolution data for aminophylline tablets. The kinetic significance of the estimated parameters of the equation is discussed. The method of analysis is compared to an approach employing an empirical equation based on a modified Weibull distribution function.
๐ SIMILAR VOLUMES
Basic problems of kinetic processing of nonisothermal data ascertained from thermal analysis measurements can be solved by isoconversional methods Analysis of the dependence of the activation energy on conversion often permits the identification of the kinetic scheme for the process This dependence