The main objectives of this study were (a) to evaluate the in vitro performance of the rapid disintegration tablets as a way to\nimprove the solid dispersions and (b) to study the in vivo pharmacokinetics of the albendazole modified formulation in dogs. Rapid\ndisintegration of tablets seems to be a key factor for efficiency of solid dispersions with regard to improvement of the albendazole\nbioavailability. The in vivo assays performed on dogs showed a marked increase in drug plasma exposure when albendazole was\ngiven in solid dispersions incorporated into rapid disintegration tablets compared with conventional solid dosage form.
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