Related Experiment Video
Updated: Jun 12, 2025

Biomechanical Characterization of Human Soft Tissues Using Indentation and Tensile Testing
Published on: December 13, 2016
Relaxation tests for the time dependent behavior of pharmaceutical tablets: A revised interpretation
Vincent Mazel1, Pierre Tchoreloff1
1Univ. Bordeaux, CNRS, Bordeaux INP, I2M, UMR 5295, F-33400 Talence, France; Arts et Metiers Institute of Technology, CNRS, Bordeaux INP, Hesam Universite, I2M, UMR 5295, F-33400 Talence, France.
Monitoring die-wall pressure during pharmaceutical powder relaxation tests helps distinguish between viscoelastic and viscoplastic behaviors. This improves understanding of strain rate sensitivity in pharmaceutical materials.
Area of Science:
- Pharmaceutical Science
- Materials Science
- Rheology
Background:
- Relaxation tests are crucial for evaluating pharmaceutical powder and tablet strain rate sensitivity.
- Interpreting these tests is challenging due to the simultaneous occurrence of viscoelasticity and viscoplasticity.
- Axial pressure alone cannot differentiate between these two phenomena as it decreases in both cases.
Purpose of the Study:
- To demonstrate how monitoring die-wall pressure during relaxation tests can differentiate viscoelastic and viscoplastic behaviors.
- To investigate the influence of compaction pressure on the dominance of these phenomena.
Main Methods:
- Theoretical analysis of pressure evolution during relaxation.
- Experimental validation using specially designed compaction cycles.
- Testing on four different pharmaceutical excipients.
Main Results:
- Die-wall pressure decreases during viscoplasticity and increases during viscoelastic relaxation.
- Viscoplasticity predominates at low compaction pressures.
- Viscoelasticity becomes more prominent at high compaction pressures.
Conclusions:
- Monitoring die-wall pressure is a viable method to separate viscoelastic and viscoplastic effects in pharmaceutical relaxation tests.
- Low pressures are suitable for assessing viscoplastic properties.
- High pressures should be avoided to prevent misinterpretation due to significant viscoelastic contributions.
Related Concept Videos
Noncompartmental Analysis: Mean Transit, Absorption and Dissolution Time
One of the key parameters is the mean transit time (MTT), which refers to the total duration required for drug molecules to transit through the body. MTT is determined by calculating the ratio of the area under the moment curve to the area...
Factors Influencing Drug Absorption: Pharmaceutical Parameters
Atomic Nuclei: Types of Nuclear Relaxation
In spin–lattice or longitudinal relaxation, the excited spins exchange energy with the surrounding lattice as they return to the lower energy level. Among several mechanisms that contribute to spin–lattice relaxation, magnetic dipolar interactions are significant. Here, the excited nucleus transfers...
One-Compartment Open Model for IV Bolus Administration: Estimation of Elimination Rate Constant, Half-Life and Volume of Distribution
Noncompartmental Analysis: Mean Residence Time
After the administration of a drug through intravenous bolus injection, the drug molecules are distributed throughout the body and remain there for varying periods. The MRT represents the average time these drug molecules stay in the...
Factors Influencing Drug Absorption: Drug Dissolution

