| Literature DB >> 30862481 |
Christel A S Bergström1, Karl Box2, René Holm3, Wayne Matthews4, Mark McAllister5, Anette Müllertz6, Thomas Rades6, Kerstin J Schäfer7, Alexandra Teleki8.
Abstract
Intrinsic dissolution rate (IDR) is the surface specific dissolution rate of a drug. In early drug development, this property (among other parameters) is measured in order to compare different polymorphs and salt forms, guide formulation decisions, and to provide a quality marker of the active pharmaceutical ingredient (API) during production. In this review, an update on different methods and small-scale techniques that have recently evolved for determination of IDR is provided. The importance of biorelevant media and the hydrodynamic conditions of dissolution are also discussed. Different preparation techniques for samples are presented with a focus on disc, particle- and crystal-based methods. A number of small-scale techniques are then described in detail, and their applicability domains are identified. Finally, an updated industrial perspective is provided about IDR's place in the early drug development process.Mesh:
Year: 2019 PMID: 30862481 DOI: 10.1016/j.ejpb.2019.03.011
Source DB: PubMed Journal: Eur J Pharm Biopharm ISSN: 0939-6411 Impact factor: 5.571