Vincent Mazel, I2M,
Université de Bordeaux
Capping and lamination are classical defects that can occur during the manufacturing of pharmaceutical tablets. Both correspond to a failure of the final tablet in a plan normal to the compaction direction. Nevertheless, they correspond to different kind of defects and even the term lamination covers in fact different kinds of defects. All these defects correspond to different failure patterns and to different failure mechanisms. As such, they are differently impacted by the product and process parameters.
In this presentation we will discuss a classification of the different defects and show the different mechanisms. The effect of classical solution like pre-compression, tapered die or press slowing down will be studied for each defects. We will also try to show how the powder/tablet mechanical behavior impacts the different defects. Finally, we will try to understand which parameters can be useful in order to anticipate the occurrence of capping/lamination at the manufacturing scale.