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Formulation of ketorlac tromethamine in semi-solid dosage forms.

مؤلف البحث
Fawzia Habib, Maha Abdel Azeem, Amal El Sayeh Fadl and Raafat El Sayed
قسم البحث
مجلة البحث
Bull. Pharm. Sci., Assiut University,
تصنيف البحث
2
عدد البحث
32(2),
سنة البحث
2009
المشارك في البحث
ملخص البحث

Ketorolac tromethamine (KT) is one of NSAIDs that has GIT, renal and hepatic disorder if taken orally. The study aimed at avoiding the adverse effects of KT by formulating it in different topical dosage form such as gel (Sodium algnate, NaCMC, HPMC, Carbopol 934 and Pluronic F127), emulgel (O/W), microemulsion and cream (O/W and W/O). The interactions between KT, polymers and other ingredients used were studied using differential scanning calorimeter (DSC) and Infra red (IR) spectroscopy. The physical properties of these formulations appearance, homogeneity, pH and viscosity were studied. The in-vitro release of KT from these formulations through cellophane membrane was carried out. The kinetic study of KT release from these formulations was also studied. In-vitro study of KT permeation in diffusion cell using rat skin from the selected formulations was carried out.
Physical investigation of KT and polymers indicated that no interaction between KT and polymers. Among the polymers used in gel formulations, HPMC and NaCMC gave the highest release rate of KT in-vitro, while pluronic F127 gave promising sustained release. In case of emulgel formulations, O/W emulgel base gave higher release than microemulsion base. Also in case of emulsion ointment base formulations, the release of KT from O/W base was higher than W/O type which gave the lowest release.
In-vitro study of KT through the diffusion cell using rat skin as biological membrane, higher permeation was obtained in case of carbopol 934 gel and O/W emulgel comparison with pluronic F127 gel which gave the lowest permeation of KT.