Use of a continuous twin screw granulation and drying system during formulation development and process optimization

• Published in: European journal of pharmaceutics and biopharmaceutics 2015-01, Vol.89, p.239-247
• Main Authors: Vercruysse, J., Peeters, E., Fonteyne, M., Cappuyns, P., Delaet, U., Van Assche, I., De Beer, T., Remon, J.P., Vervaet, C.
• Format: Article
• Language: English
• Subjects: Bone Screws; Cellulose - chemistry; Chemistry, Pharmaceutical - methods; Continuous twin screw granulation and drying; Desiccation - methods; Excipients - chemistry; Formulation development; Granule and tablet quality; Particle Size; Pressure; Process optimization; Process scale-up; Repeatability; Starch - analogs & derivatives; Starch - chemistry; Stearic Acids - chemistry; Tablets - chemistry; Technology, Pharmaceutical - methods; Temperature; Water - chemistry
• ISSN: 0939-6411; 1873-3441
• DOI: 10.1016/j.ejpb.2014.12.017

[Display omitted] •Deviating quality attributes were obtained during the first 30min of the 1h run.•No deviating granule and tablet quality was observed during the shutdown phase.•Processing of material in a single cell was repeatable.•Materials processed in a single cell were predictive for full-scale manufacturing.•Tablet quality from ConsiGma™-1 system was predictive for ConsiGma™-25 system. Since small scale is key for successful introduction of continuous techniques in the pharmaceutical industry to allow its use during formulation development and process optimization, it is essential to determine whether the product quality is similar when small quantities of materials are processed compared to the continuous processing of larger quantities. Therefore, the aim of this study was to investigate whether material processed in a single cell of the six-segmented fluid bed dryer of the ConsiGma™-25 system (a continuous twin screw granulation and drying system introduced by GEA Pharma Systems, Collette™, Wommelgem, Belgium) is predictive of granule and tablet quality during full-scale manufacturing when all drying cells are filled. Furthermore, the performance of the ConsiGma™-1 system (a mobile laboratory unit) was evaluated and compared to the ConsiGma™-25 system. A premix of two active ingredients, powdered cellulose, maize starch, pregelatinized starch and sodium starch glycolate was granulated with distilled water. After drying and milling (1000μm, 800rpm), granules were blended with magnesium stearate and compressed using a Modul™ P tablet press (tablet weight: 430mg, main compression force: 12kN). Single cell experiments using the ConsiGma™-25 system and ConsiGma™-1 system were performed in triplicate. Additionally, a 1h continuous run using the ConsiGma™-25 system was executed. Process outcomes (torque, barrel wall temperature, product temperature during drying) and granule (residual moisture content, particle size distribution, bulk and tapped density, hausner ratio, friability) as well as tablet (hardness, friability, disintegration time and dissolution) quality attributes were evaluated. By performing a 1h continuous run, it was detected that a stabilization period was needed for torque and barrel wall temperature due to initial layering of the screws and the screw chamber walls with material. Consequently, slightly deviating granule and tablet quality attributes were obtained during the start-up phase of the 1h run. For the single cell runs, gran