Affiliation:
1. Department of Pharmaceutical Chemistry, University of Pavia, 12 viale Taramelli, 27100 Pavia, Italy
Abstract
Abstract
The preparation of hydrophilic matrix tablets able to release naftazone, a water-insoluble drug, into an aqueous medium at a constant rate (zero-order dissolution) is described. Enhancement of dissolution rate of the drug was achieved using cross-linked carmellose sodium, β-cyclodextrin or hydroxypropyl-β-cyclodextrin. Hypromellose was used as a water-gelling polymer. Tablets could be prepared that released naftazone at a constant rate over 16 h.
Publisher
Oxford University Press (OUP)
Subject
Pharmaceutical Science,Pharmacology
Reference12 articles.
1. β-Cyclodextrin as an excipient in solid oral dosage forms;Bootsma;Int. J. Pharm.,1989
2. Swelling properties of disintegrants;Caramella;Acta Pharm. Techn.,1984
3. The role of swelling in the disintegration process;Caramella;Int. J. Pharm. Techn. Prod. Mfr.,1984
4. The effect of magnesium stearate and polytetrafluoroethylene as lubricants in direct compression of acetylsalicylic acid;Conte;Il Farmaco Ed. Prat.,1972
5. Particle size of drugs and its relationship to absorption and activity;Fincher;J. Pharm. Sci.,1968
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