Saudi Pharmaceutical Journal · 2015 · 39 citations · 3 references
PharmacyPharmaceuticsPharmacologyBioavailabilityDrug DeliveryPharmaceutical FormulationGastrointestinal AbsorptionGastrointestinal PharmacologyTablet DesignCoated TabletsEnteric-coated Dosage FormsFormulation Performance TestingGastrointestinal ReleaseIn-vitro CharacterizationRelease Condition MonitoringRelease Rate EstimationSimulated Gastric Fluid
The aim of this study was to prepare the rosiglitazone sodium enteric-coated tablets and investigate its release rate. The rosiglitazone sodium enteric-coated tablet was prepared by single punch tablet press using substituted hydroxypropyl cellulose and polyvinylpyrrolidone (PVP). The release rate from the enteric-coated tablet of rosiglitazone sodium was evaluated. The release rate study showed that few rosiglitazone sodium was released from enteric coated formulation within 2 h in simulated gastric juice, while it released more than 80% of the labeled amount in 30 min in simulated intestinal juice. The preparing method of rosiglitazone sodium enteric-coated tablets was simple and had a good reproducibility. The release condition and determined methods could be used for the routine determinations of rosiglitazone sodium enteric-coated tablets.
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Prevalence of Diabetes among Men and Women in China
Wenying Yang, Juming Lu, Jianping Weng et al. · New England Journal of Medicine · 2010 · 3.1K citations
Mechanisms of Early Insulin-Sensitizing Effects of Thiazolidinediones in Type 2 Diabetes
Julia Tonelli, Weijie Li, Preeti Kishore et al. · Diabetes · 2004 · 247 citations · Full text