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Standardized flow-cell method as an alternative to existing pharmacopœial dissolution testing
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1989
Year
Pharmacopœial DissolutionAvailable ApparatusPharmacokinetic ModelingPreclinical Drug EvaluationDrug PowdersMedicineDrug PurityBioequivalenceForensic ToxicologyActive IngredientPharmaceutical TechnologyMethodological StandardsLiquid ChromatographyClinical ChemistryPharmacologyFlow-cell MethodPharmacokineticsChromatography
Methodological standards achieved in the past are reviewed, with reference to commercially available apparatus. This includes application to conventional tablets and capsules, as well as drug powders and granulated materials, adsorbates and suppositories