The pharmaceutical industry has been shifting towards continuous manufacturing, specifically for tablet production. Compared to batch processing, continuous tableting exhibits higher process efficiency, better process control, reduced footprint, and consistent product quality. Understanding mass flow variability and feed factor profile of raw materials in the loss-in-weight feeding process is essential for controlling continuous processes. Current literature has highlighted correlations between material properties and feeding performance. However, research still lacks an assessment of how feeder set-up options impact this performance. This paper aims to fill the existing gap between material properties and feeder output to expedite the process development stage. A selection of commercially available excipients, crystalline APIs, spray-dried excipients, and protein-based excipients (nineteen in total) were characterized in terms of physical properties and rheological behavior. Volumetric feeding trials were conducted in a loss-in-weight feeder to obtain the feeding performance (mass flow RSD and feed factor profile curve). Partial least squares regression demonstrated that feeder performance can be estimated from material density, flowability, cohesion, charge density, and porosity. Additionally, experiments were conducted to assess the impact of feeding set-up options on feeding dynamics, enabling the development of a workflow for set-up and operating range definition. Applying this workflow to five different materials demonstrated sufficient accuracy in defining the feeder set-up parameters when compared to the experimental data results. The developed data-driven approach minimizes both material and time requirements, making it more efficient than a trial-and-error approach, which is essential for accelerating development.
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http://dx.doi.org/10.1016/j.ijpharm.2025.125434 | DOI Listing |
Int J Pharm
March 2025
Research Institute for Medicines (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-033 Lisboa, Portugal. Electronic address:
The pharmaceutical industry has been shifting towards continuous manufacturing, specifically for tablet production. Compared to batch processing, continuous tableting exhibits higher process efficiency, better process control, reduced footprint, and consistent product quality. Understanding mass flow variability and feed factor profile of raw materials in the loss-in-weight feeding process is essential for controlling continuous processes.
View Article and Find Full Text PDFInt J Pharm
February 2025
Laboratory of Pharmaceutical Technology, Department of Pharmaceutics, Ghent University, Ottergemsesteenweg 460, B-9000 Ghent, Belgium. Electronic address:
In recent years, CM has become increasingly popular in the pharmaceutical industry for the production of OSD forms. Most of the newly developed APIs nowadays are extremely cohesive and sticky with a mean particle size particle of <100 μm, a wide PSD and a high tendency to agglomerate, making them difficult to accurately dose using loss-in-weight equipment during CM. In this research paper, the effect of various glidants on the volumetric and gravimetric feeding of several APIs was assessed.
View Article and Find Full Text PDFInt J Pharm
August 2024
Department of Chemical Engineering, University of Puerto Rico at Mayaguez, Puerto Rico 00681, United States. Electronic address:
Continuous manufacturing has the potential to offer several benefits for the production of oral solid dosage forms, including reduced costs, low-scale equipment, and the application of process analytical technology (PAT) for real-time process control. This study focuses on the implementation of a stream sampler to develop a near infrared (NIR) calibration model for blend uniformity monitoring in a continuous manufacturing mixing process. Feeding and mixing characterizations were performed for three loss-in-weight feeders and a commercial continuous mixer to prepare powder blends of 2.
View Article and Find Full Text PDFInt J Pharm X
June 2024
Department of Systems Science, Kyoto University, Yoshida-honmachi, Sakyo-ku, Kyoto 6068501, Kyoto, Japan.
In continuous pharmaceutical manufacturing processes, it is crucial to control the powder flow rate. The feeding process is characterized by the amount of powder delivered per screw rotation, referred to as the feed factor. This study aims to develop models for predicting the feed factor profiles (FFPs) of two-component mixed powders with various formulations, while most previous studies have focused on single-component powders.
View Article and Find Full Text PDFPharmaceutics
May 2023
School of Chemical Engineering, University of Birmingham, Birmingham B15 2TT, UK.
The pharmaceutical industry is undergoing a paradigm shift towards continuous processing from batch, where continuous direct compression (CDC) is considered to offer the most straightforward implementation amongst powder processes due to the relatively low number of unit operations or handling steps. Due to the nature of continuous processing, the bulk properties of the formulation will require sufficient flowability and tabletability in order to be processed and transported effectively to and from each unit operation. Powder cohesion presents one of the greatest obstacles to the CDC process as it inhibits powder flow.
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