The aim of this study was to investigate liquid penetration into both cylindrical and convex hydrophobic matrix tablets and to relate the changes in tablet structure to drug release. Starch acetate with degree of substitution of 2.7 was used as a hydrophobic matrix former and anhydrous caffeine as a freely soluble model drug. Phenolred was used as a colouring agent to enhance the visual detection of the liquid boundary movements, which were examined in axial and radial directions for both types of tablets. The tablets started to expand during the dissolution, resulting in cracking as the liquid boundary penetrated into tablet. The cracking influences drug release by shortening the diffusion path and decreasing the tortuosity. The liquid boundaries proceed differently in cylindrical and convex tablets, this being attributable to differences in pore structure and density distribution. Cylindrical tablets are quite homogeneous in terms of density, but convex tablets have more porous areas at the domes of the tablet. (c) 2006 Elsevier B.V. All rights reserved.
机构:
Thammasat Univ, Fac Pharm, Res Unit Smart Mat & Innovat Technol Pharmaceut A, Pathum Thani 12120, ThailandThammasat Univ, Fac Pharm, Res Unit Smart Mat & Innovat Technol Pharmaceut A, Pathum Thani 12120, Thailand
机构:
Univ Helsinki, Fac Pharm, Ind Pharm, Helsinki, Finland
AstraZeneca R&D, Formulat Sci, S-43183 Molndal, SwedenUniv Helsinki, Fac Pharm, Ind Pharm, Helsinki, Finland
Heiman, Johanna
Tajarobi, Farhad
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AstraZeneca R&D, Formulat Sci, S-43183 Molndal, SwedenUniv Helsinki, Fac Pharm, Ind Pharm, Helsinki, Finland
Tajarobi, Farhad
Gururajan, Bindhumadhavan
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AstraZeneca R&D, Formulat Sci, S-43183 Molndal, SwedenUniv Helsinki, Fac Pharm, Ind Pharm, Helsinki, Finland
Gururajan, Bindhumadhavan
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Juppo, Anne
Abrahmsen-Alami, Susanna
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AstraZeneca R&D, Formulat Sci, S-43183 Molndal, SwedenUniv Helsinki, Fac Pharm, Ind Pharm, Helsinki, Finland