Investigation of drug release from suspension using FTIR-ATR technique: part II. Determination of dissolution coefficient of drugs

Citation
Bd. Hanh et al., Investigation of drug release from suspension using FTIR-ATR technique: part II. Determination of dissolution coefficient of drugs, INT J PHARM, 204(1-2), 2000, pp. 151-158
Citations number
7
Categorie Soggetti
Pharmacology & Toxicology
Journal title
INTERNATIONAL JOURNAL OF PHARMACEUTICS
ISSN journal
03785173 → ACNP
Volume
204
Issue
1-2
Year of publication
2000
Pages
151 - 158
Database
ISI
SICI code
0378-5173(20000825)204:1-2<151:IODRFS>2.0.ZU;2-D
Abstract
Fourier transform infrared attenuated total reflectance (FTIR-ATR) spectros copy was applied to a release experiment in order to determine the dissolut ion coefficient of drug particles in heterogeneous semisolid formulations. The drug release experiment was carried out using ketoconazole suspended in Vaseline with various amounts of paraffinum liquidum as donor and an artif icial dodecanol-collodion (DDC) membrane as acceptor compartment. Monitorin g changes in IR bands due to ketoconazole the decrease of the drug content near the ATR crystal ointment was followed as a function of time. A mathema tical model based on Fick's second law with a source term was used to deriv e the apparent dissolution coefficient K-dis by numerical fitting the exper imental data. It was found that K-dis is dependent on the fraction of paraf finum liquidum in the suspension. Taking into account all experimental para meters required, the transport process was simulated and discussed in terms of drug concentration - time and drug concentration - distance profiles. C alculating the area under the mass - time curve it was tried to predict the 'dermal bioavailability' in the acceptor (AUC(a)). (C) 2000 Published by E lsevier Science B.V.