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D-optimal mixture design was applied to optimize the level of the main ingredients "i.e".e
The D-optimal mixture design was applied to optimize the ratio of the three kinds of components in the media.
D-optimal mixture experimental design was applied to optimize the formulation variables; oil phase X1 (Clove oil), surfactant X2 (Tween-80) and co-surfactant X3 (Polyethylene glycol-400).
A central composite design was applied to optimize the critical chromatographic parameters.
A two-level fractional factorial experimental design was applied to optimize the ultrasound-assisted extraction.
A 24 factorial design was applied to optimize the drug formulation.
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A central composite design is applied to optimize the major influential manipulate variables.
The Box Behnken experimental design was applied to optimize and trial the robustness of the HSA nanoparticle preparation method.
Molecular modeling and iterative drug design were applied to optimize this series.
A central composite design was applied to optimize its lignocellulolytic as well as cellulolytic enzyme production in submerged-state fermentation.
A Doehlert experimental design was applied to optimize its lignocellulolytic enzyme production in solid-state fermentation.
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