Drug Development and Industrial Pharmacy · 1991 · 13 citations · 4 references
PharmacyPharmaceuticsPharmacokineticsBioavailabilityDrug DeliveryPharmaceutical FormulationDrug DispositionDrug DissolutionDrug Release From Dosage FormsDrug SolubilityFormulation Effects On BioavailabilityOral Bioavailability EnhancementDissolution Of Solid DispersionsDissolution Rate AnalysisDissolution Rate DeterminationPharmacokinetics Of Polymer CarriersPoorly Water-soluble DrugsSolubility Determination
Coprecipitates of trimethoprim have been prepared by solvent method using polyethylene glycols 4000, 6000 and 9000, and polyvinylpyrrolidone (M.W. 40,000) as water soluble carriers. A marked increase in the dissolution rate of trimethoprim in the coprecipitates was observed compared with that of the drug alone. Coprecipitates with polyethylene glycol 6000 (1:2) showed faster release as well as bioavailability of the drug in human volunteers.
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