Skip to main content
18.188.76.209

Lubricant Sensitivity of Direct Compression Grades of Lactose in Continuous and Batch Tableting Process

By Gerald A. Hebbink1; Pauline H. M. Janssen2; Jurjen H. Kok1; Lorenzo Menarini3; Federica Giatti3; Caterina Funaro3; Salvatore Fabrizio Consoli3; Bastiaan H. J. Dickhoff1

1. DFE Pharma GmbH & Co. KG, 47574 Goch, Germany 2. DFE Pharma GmbH & Co. KG, 47574 Goch, Germany and Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, 9713 AV Groningen, The Netherlands 3. IMA S.p.A. Active Division, 40064 Ozzano dell’Emilia Bologna, Italy

Published on

Abstract

Modern pharmaceutical manufacturing based on Quality by Design and digitalisation is revolutionising the pharmaceutical industry. Continuous processes are promoted as they increase efficiency and improve quality control. Compared to batch blending, continuous blending is easier to scale and provides advantages for achieving blend homogeneity. One potential challenge of continuous blending is the risk of over-lubrication. In this study, blending homogeneity and lubricant sensitivity are investigated for both batch and continuous processes. Given their distinct chemical structures and morphologies, anhydrous lactose and granulated lactose are expected to exhibit varying sensitivities to changes in process settings across both technologies. The findings suggest that both lactose grades provide highly stable blends that can be safely utilised in both batch and continuous modes. Optimisation should focus on process variables, such as the quality of loss-in-weight feeders used for dosing low doses of ingredients. The most significant process parameter for lubricant sensitivity was the type of lactose used. Anhydrous lactose produced harder tablets than the more porous granulated lactose but was more sensitive to lubrication at the same settings. The magnesium stearate content and its interaction with the type of lactose are also critical factors, with magnesium stearate having a counterproductive impact on tabletability.

Journal

Pharmaceutics

DOI

10.3390/pharmaceutics15112575

Type of publication

Article

Tags