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Dissolution Testing of Hardly Soluble Materials by Surface Sensitive Techniques: Clotrimazole from an Insoluble Matrix
Authors:Heike M. A. Ehmann  Sascha Winter  Thomas Griesser  Roman Keimel  Simone Schrank  Andreas Zimmer  Oliver Werzer
Affiliation:1. Institute of Pharmaceutical Sciences, Department of Pharmaceutical Technology, University of Graz, Universitit?tsplatz 1, 8010, Graz, Austria
2. Institute of Physical and Theoretical Chemistry, University of Graz, Heinrichstra?e 28, 8010, Graz, Austria
3. Chemistry of Polymeric Materials, Montanuniversit?t Leoben, Otto-Gl?ckelstrasse 2, 8700, Leoben, Austria
4. Institute for Process and Particle Engineering, University of Technology Graz, Inffeldgasse 13, 8010, Graz, Austria
Abstract:

Purpose

The low aqueous solubility of many drugs impedes detailed investigation as the detection limit of standard testing routines is limited. This is further complicated within application relevant thin films typical used in patches or stripes for buccal or topical routes.

Methods

In this work a model system is developed based on spin – casting technique allowing defined clotrimazole and clotrimazole – polystyrene composite films preparation at a solid surface. Various highly sensitive techniques including quarz crystal microbalance (QCM), X-ray reflevtivity (XRR) and X-ray photon spectroscopy (XPS) are used to investigate the drug release over time into an aqueous media.

Results

The results reveal a steady drug release for both samples over the course of the experiments but with the release from the composite being significantly slower. In addition the dissolution rate of the clotrimazole sample initially increases up to 30 min after which a decrease is noted. XRR shows that this is a result of surface roughening together with film thickness reduction. The results for the composite show that the release in the composite film is a result of drug diffusion within the matrix and collapsing PS film thickness whereby XPS shows that the amount of clotrimazole at the surface after 800 min immersion is still high.

Conclusion

It can be stated that the applied techniques allow following low mass drug release in detail which may also be applied to other systems like pellets or surface loaded nano-carriers providing information for processing and application relevant parameters.
Keywords:
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