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A Numerical Model of a Drug Particle Dissolving in a Dissolution Test Apparatus
Author(s) -
McMahon Niall M.,
Crane Lawrence J.,
Ruskin Heather J.,
Crane Martin,
D'Arcy Deirdre M.,
Healy AnneMarie,
Corrigan Owen I.
Publication year - 2009
Publication title -
pamm
Language(s) - English
Resource type - Journals
ISSN - 1617-7061
DOI - 10.1002/pamm.200910297
Subject(s) - dissolution , dissolution testing , particle size , particle (ecology) , drug delivery , mass transfer , materials science , chemistry , nanotechnology , chemical engineering , chromatography , engineering , oceanography , biopharmaceutics classification system , geology
The dissolving compact, or tablet, is the most widely used method of drug delivery. Dissolution tests are used to ensure consistency during tablet manufacture, to assess the dissolution characteristics of a particular tablet design, to establish in vitro/in vivo correlations, and to predict how the drug will perform in the body. Dissolution tests also form a part of the drug approval process. The United States Pharmacopeia (USP) Type 2 Paddle Dissolution Apparatus,from here on referred to as the USP apparatus, is a standard dissolution test device, used by the Food and Drug Administration (FDA) and the pharmaceutical industry. Although the USP apparatus is much used, detailed theoretical descriptions of its characteristics are still not well developed. This work considers one possible end state of a dissolving tablet, i.e. fragmentation into small particles with dissolution continuing from the disintegrated solid masses. A framework for calculating the motion of and mass transfer from a drug particle moving through the USP apparatus is outlined. Calculations demonstrate that small particles move with the USP apparatus flow and that, for small particles below a critical diameter, natural convection and radial diffusion dominate, i.e. forced convection effects can be neglected for small particles. (© 2009 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim)