Related Experiment Video
Updated: Aug 17, 2026

Reliable Mechanochemistry: Protocols for Reproducible Outcomes of Neat and Liquid Assisted Ball-mill Grinding Experiments
Published on: January 23, 2018
Applicability of the Vreeman-Sun equation - power law mixing rule (VS-PL) model for predicting tabletability of
Zijian Wang1, Vedant Bhagali2, Gerrit Vreeman3
1Pharmaceutical Materials Science and Engineering Laboratory, Department of Pharmaceutics, College of Pharmacy, University of Minnesota, MN 55455, USA; Bristol Myers Squibb, 1 Squibb Dr, New Brunswick, NJ 08901, USA.
Abstract:
Tabletability, which quantifies a powder's ability to be transformed into a tablet with a specified mechanical strength under an applied compaction pressure, is a critical material property in tablet formulation development. A predictive model based on the Vreeman-Sun equation, combined with a power-law mixing rule (VS-PL), has recently been proposed to estimate the tabletability of binary mixtures from those of individual components. In this study, the applicability of this model across diverse materials and formulation conditions was systematically evaluated using sixty unique binary mixtures, two ternary mixtures, and one five-component system comprising common pharmaceutical excipients and active pharmaceutical ingredients. The model demonstrated good predictive performance for most binary mixtures and accurately predicted the tabletability of the ternary mixtures and the quinary formulation. Particle size variation (30-180 µm) was found to have minimal impact on model performance within the investigated systems, and the model was applicable to formulations lubricated with magnesium stearate. However, predictions were less reliable for formulations involving very hard materials and compositions below the percolation threshold. Despite these limitations, the predictive framework has the potential to facilitate material-sparing and efficient digital design of high-quality tablet formulations.
Related Concept Videos
Theories of Dissolution: The Danckwerts' Model and Interfacial Barrier Model
One-Compartment Open Model for IV Bolus Administration: Estimation of Elimination Rate Constant, Half-Life and Volume of Distribution
In Vitro Drug Dissolution: Compendial Testing Models I
One-Compartment Open Model for IV Bolus Administration: General Considerations
The drug's presence in the body is defined by an equation representing the difference between the rates of drug entry and exit. Key parameters—elimination rate constant, half-life,...
Theories of Dissolution: Diffusion Layer Model
This process starts with a thin layer, saturated with the drug, forming at the interface between the solid and liquid. The solute then diffuses from this layer into the main solution. The Noyes-Whitney equation suggests that the rate of dissolution relies on the diffusion...
Two-Compartment Open Model: IV Bolus Administration
The disparity between drug input and the sum of drug transfer rates between...
