Mathematically Modelling the Dissolution of Solid Dispersions

Meere, M., Mcginty, S. and Pontrelli, G. (2017) Mathematically Modelling the Dissolution of Solid Dispersions. In: Equadiff 2017 Conference, Bratislava, Slovakia, 24-28 Jul 2017, pp. 341-348. ISBN 9788022747578

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Publisher's URL: http://www.iam.fmph.uniba.sk/amuc/ojs/index.php/equadiff/article/view/815

Abstract

A solid dispersion is a dosage form in which an active ingredient (a drug) is mixed with at least one inert solid component. The purpose of the inert component is usually to improve the bioavailability of the drug. In particular, the inert component is frequently chosen to improve the dissolution rate of a drug that is poorly soluble in water. The construction of reliable mathematical models that accurately describe the dissolution of solid dispersions would clearly assist with their rational design. However, the development of such models is challenging since a dissolving solid dispersion constitutes a non-ideal mixture, and the selection of appropriate forms for the activity coefficients that describe the interaction between the drug, the inert matrix, and the dissolution medium is delicate. In this paper, we present some preliminary ideas for modelling the dissolution of solid dispersions.

Item Type:Conference Proceedings
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Mcginty, Dr Sean
Authors: Meere, M., Mcginty, S., and Pontrelli, G.
College/School:College of Science and Engineering > School of Engineering > Biomedical Engineering
ISBN:9788022747578

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