Autor: |
Hamman H; a Centre of Excellence for Pharmaceutical Sciences , North-West University , Potchefstroom , South Africa., Hamman J; a Centre of Excellence for Pharmaceutical Sciences , North-West University , Potchefstroom , South Africa., Wessels A; a Centre of Excellence for Pharmaceutical Sciences , North-West University , Potchefstroom , South Africa., Scholtz J; a Centre of Excellence for Pharmaceutical Sciences , North-West University , Potchefstroom , South Africa., Steenekamp J; a Centre of Excellence for Pharmaceutical Sciences , North-West University , Potchefstroom , South Africa. |
Jazyk: |
angličtina |
Zdroj: |
Pharmaceutical development and technology [Pharm Dev Technol] 2019 Feb; Vol. 24 (2), pp. 145-156. Date of Electronic Publication: 2018 Feb 27. |
DOI: |
10.1080/10837450.2018.1435691 |
Abstrakt: |
The SeDeM Expert Diagram System (SeDeM EDS) was originally developed to provide information about the suitability of powders to produce direct compressible tablets. Multiple-unit pellet systems (MUPS) are dosage forms consisting of pellets compressed into tablets or loaded into hard gelatin capsules. The aim of this study was to apply the SeDeM EDS to different size pellets (i.e. 0.5, 1.0, 1.5, 2.0, and 2.5 mm) containing different APIs (i.e. doxylamine, ibuprofen or paracetamol) to determine which properties should be corrected to yield MUPS tablet formulations. The SeDeM parameter tests were conducted on the pellets, selected excipients, intermediate blends, and final blends. The study showed that the properties of the pellets depended on the active ingredient and pellet size. The SeDeM compressibility indices indicated that the final pellet blends should be suitable for compression into MUPS tablets. MUPS tablets were prepared from the final blends and evaluated in terms of physico-chemical properties and dissolution profiles. Only three of the MUPS tablet formulations containing ibuprofen and one MUPS tablet formulation containing paracetamol failed content uniformity. The water solubility of the APIs as well as the pellet size (surface area exposed to the dissolution medium) attributed to the difference in drug dissolution rate. |
Databáze: |
MEDLINE |
Externí odkaz: |
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