Abstract

Starting point of the presented study were abrasion effects occurring during a twin screw wet granulation (TSG) process of a new chemical entity (NCE) formulation, resulting in gray spots on the final tablets. Several actions and systematic changes of equipment and process parameter settings of TSG process were conducted which reduced the visual defect rate of the tablets, i.e., gray spots on the surface, below the specification limit. To understand the rationale and mechanism behind these improvements, correlations of defect rates and wall friction measurements using a Schulze ring shear tester were evaluated. To check the suitability of the method, a broad range of wall materials as well as powder formulations at various moisture levels were investigated with regard to their wall friction angle. As differences in wall friction angle could be detected, further experiments were conducted using wall material samples made out of different screw materials for TSG. Evaluation of these screw wall material samples gave first hints, which screw materials should be preferred in regard of friction for TSG process. In the finally presented case study, wall friction measurements were performed using the above mentioned NCE formulation with known abrasion issues at TSG processing. The results confirmed that changes which led to a reduced visual defect rate of tablets correlated with a decreased wall friction angle. The results suggest wall friction measurements as a potent tool for equipment selection and establishment of a suitable process window prior to conducting TSG experiments.Graphical abstract

Highlights

  • The aim of pharmaceutical production is to always result in a final drug product of the desired quality

  • The measured parameter describing the friction between a powder and a surface is the wall friction angle, which is accessible by various wall friction testers described in literature [2, 6, 12, 14]

  • An increase of average WFA φ [°] with increasing moisture level [%] - compared at defined normal stresses σw [Pa] - was obtained

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Summary

Introduction

The aim of pharmaceutical production is to always result in a final drug product of the desired quality. Key for this aim is proper process understanding, including potential issues and their associated risks, which may occur during a pharmaceutical process. To understand and balance the effect of friction, a supportive method should facilitate a more rational selection of equipment and process settings. 10 g for wall friction measurement) at reduced measuring periods [14] and was selected to be used in this study. Apart from this practical considerations, Schulze described the big advantage of

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