Drug Development and Industrial Pharmacy · 2006 · 15 citations · 7 references
PharmacyPharmaceuticsDissolution TestingDosage Form DesignPharmaceutical FormulationDrug FormulationPharmaceutical StabilityStability Of Pharmaceutical FormulationsTablet DesignTablet FormulationTablet TechnologyBatch-to-batch ComparisonBatch-to-batch Consistency AssessmentCrushingMean Dissolution TimeMethod Robustness TestingRobustness TestingRobustness Testing MethodologyTablet Formulation Design
A total of 45 experiments were carried out to evaluate the robustness of two similar tablet formulations--a product of two strengths--with respect to normal batch-to-batch variation of the excipients and the active pharmaceutical ingredient. The formulations consist of 10 ingredients. Because of the differing amounts of active pharmaceutical ingredients, the two formulations also differ in the amounts of two of the diluents and one of the binders. The excipients and active pharmaceutical ingredient were characterized in terms of multiple variables, and principal properties were calculated with principal component analysis. A Plackett and Burman design was applied to the principal properties. The relationships between the design factors and two responses, mean disintegration time and mean crushing strength, were evaluated by using regression methods. Both formulations were found to be robust under controlled conditions.
7
Svante Wold, Kim H. Esbensen, Paul Geladi · Chemometrics and Intelligent Laboratory Systems · 1987 · 11.5K citations
THE DESIGN OF OPTIMUM MULTIFACTORIAL EXPERIMENTS
R. L. Plackett, J. P. Burman · Biometrika · 1946 · 3.8K citations
Svante Wold, Michael Sjöstróm, Rolf Carlson et al. · Analytica Chimica Acta · 1986 · 104 citations