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Chris O’Callaghan is senior product manager at Innopharma Technology, Dublin, Ireland, email@example.com.
Ian Jones, PhD, is founder and CEO of Innopharma Technology and Innopharma College of Applied Sciences, Dublin
Caroline McCormack is process laboratory manager at Innopharma Technology, Dublin, Ireland.
Luke Kiernan is a PhD student at the Technological University Dublin in Ireland.
Gavin Walker, PhD, is professor and director of the Synthesis and Solid State Pharmaceutical Centre at the University of Limerick in Ireland.
Gareth Clarke is Multieye Product Manager, Innopharma Technology, Dublin,Ireland
Advanced dynamic process control of a fluid-bed granulation process using PAT data improves product quality.
Globally, there is an increasing trend toward the use of Industry 4.0 principles, with the Industrial Internet of Things (IIoT) being a key component, while regulators are actively encouraging pharmaceutical companies to modernize their approaches to drug development and manufacturing to deliver higher quality products. Better process understanding, drug product development, and manufacturing throughout the commercial lifecycle of drug products will lead to faster time-to-market and a more reliable, predictable supply chain (1).
Adopting several of the tools and technologies which are part of the current Industry 4.0 revolution (e.g., process analytical technology [PAT], big data analytics, manufacturing intelligence, in-process control, and cloud architecture) into everyday pharmaceutical product development and commercial manufacturing may provide an effective solution to many manufacturing quality challenges. Adoption of these technologies would also dramatically improve productivity while maintaining competitive advantage and reducing costs for the manufacturer (2,3).
This article presents a practical application of Industry 4.0 architecture with commercially available technology solutions and demonstrates how the system can be implemented to reduce risks associated with traditional fluid-bed granulation manufacturing processes.
Fluid-bed wet granulation involves agglomerating a mix of dry primary powder particles (APIs and excipients) by the addition of a granulating solution in a fluid-bed granulator. In the subsequent drying phase, control is crucial because over-drying can lead to increased attrition and fracture of the product, while insufficient drying can result in bed stalling, poor flow, and product stability issues (4). The traditional control approach is recipe driven and largely operator dependent, with minimal provisions for the impacts of raw material or atmospheric variations, both of which are known to affect final granule properties (5).
The automated approach described in this article resulted in greater in-process control and repeatability as well as less batch-to-batch variation. The controller design presented here is intended as a novel example to highlight the flexibility and potential when developing this type of automated, control-driven approach.
Formulation. A placebo formulation was used for all batches. It consisted of a mixture of lactose (1 kg Pharmatose 200M, DFE Pharma) and microcrystalline cellulose (0.5 kg AvicelPH-101 NF, DuPont). The liquid binder was an aqueous solution of polyvinylpyrrolidone (1 L, 5.8% w/w, Plasdone K-90, Ashland). Materials were supplied by IMCD Ireland.
Process equipment. Fluid bed granulation was performed in a granulator (Glatt GPCG2) equipped with a particle analyzer (Eyecon2, Innopharma Technology) and near infrared (NIR) spectrophotometer (Multieye2, Innopharma Technology) measuring particle size distribution and product moisture content, respectively. The equipment is shown in Figure 1. The automated process control platform (SmartX, Innopharma Technology) provided time-aligned data aggregation of process parameter data, PAT data, and environmental sensor data.
Controller development is complex and requires a thorough understanding of the process, including critical process parameters (CPPs), their impact on critical quality attributes (CQAs), and the required process specifications. In this case, information on the process design space and optimum control was derived from retrospective analysis of more than 160 batches run on the test-bed system (SmartX Innopharma Technology), while further detailed experimentation was performed to quantify the differences in end-product quality between the results of this advanced dynamic process control (ADPC) approach and the results using a traditional control approach.
The first step in the development was to clearly define the control logic for each process phase. This included identification of key dynamic control relationships, establishing fixed setpoints as well as phase and process endpoint criteria. Once configured, this flexible control logic was then implemented and executed via a process-centric scripting environment within the integrated ADPC module.
Throughout the process, real-time PAT data and process sensor data from the fluid-bed system and environmental systems provided a continual input feed to the controller. The controller used this information to make scenario-based decisions on how to respond to process deviations as well as required process changes, including phase changes and endpoint detection.
For the ADPC example presented in this article, five process phases were defined: empty heating, material heating, spraying I, spraying II, and final drying. Figure 2 describes the five process phases and their corresponding key set-points and endpoint criteria.
Spraying is divided into two phases to demonstrate how PAT measurements may be implemented to achieve in-process control. Additionally, the two phases are designed with the intention to help mitigate against product attrition as typically observed during final drying, thus delivering more consistent endpoint particle size with less batch-to-batch variation. Spraying I is defined by rapid wetting and maximum growth, while Spraying II is defined by further hardening of the granules through reduced spray rate and increased moisture removal to mitigate against product attrition during the drying phase.
A specific moisture-content reduction rate was empirically determined to achieve a quasi-stable median volume distribution (Dv50) particle size while allowing for faster control reaction and, therefore, minimized process deviations as compared to controlling directly based on particle size.
ADPC controller. The series of CQA and CPP profiles shown in Figure 3 are taken from one of the fluid-bed granulation processes executed by the ADPC controller that was developed; these profiles demonstrate the control method’s capabilities.
Dynamic control relationships. The key relationship between spray rate and Dv50 particle size can be observed between Figure 3a (top) and 3c (bottom). The controller sets the Dv50 particle size target to 450 µm for the duration of spraying and uses real-time particle size data, as measured by the Eyecon2, to monitor the growth profile. During Spraying I, a fixed spray rate is maintained for rapid moisture addition and growth until the target particle size is reached. On entering Spraying II, the target particle size is maintained by following the empirical target moisture-content profile.
This profile is maintained by dynamic control of the spray rate based on real-time moisture content data. Comparing Figure 3b (middle) and 3c, modulation of the spray rate after a brief delay can be observed in response to small deviations of the moisture content trend either above or below the target moisture content profile (see Figure 3b, dashed line labeled ideal moisture overlay). This process slowly dries the granulate to 5%, which is the trigger to transition to the final drying phase.
Another novel aspect of this control approach can be observed in Figure 3b, where the effect of linking air flow rate to moisture content during the Spraying I phase can be seen. This approach allows optimum fluidization to be maintained while the bed becomes heavier and more cohesive, avoiding both the attrition and efficiency impacts of over-fluidizing, and the under-fluidizing risk of bed-stalling.
End-product quality. Endpoint Dv50 particle size values from a number of granulation batches manufactured with the ADPC controller were compared to the endpoint Dv50 particle size values from earlier batches manufactured using a non-ADPC controlled, recipe-driven approach. A significant difference in endpoint product consistency is apparent between the two approaches.
Figure 4a (left) illustrates a significantly wider distribution of endpoint Dv50 particle sizes for batches manufactured via the non-ADPC controlled approach, with variation of 171 µm from the smallest to largest Dv50 value. Comparing batches manufactured with the ADPC controller, a tighter distribution in endpoint Dv50 particle size values is evident, with variation of only 46 µm reported from smallest to largest Dv50 value. These results demonstrate the consistency in batch-to-batch particle size that can be achieved by implementing such a control approach within a fluid-bed granulation process. The ability to achieve greater particle size control via the ADPC controller approach leads to more consistent endpoint particle size and less variation between batches.
Endpoint moisture content values analyzed using the at-line loss-on-drying (LOD) methodology were compared for both control approaches. There is a significant difference in the endpoint LOD values for both of these approaches, primarily due to the non-ADPC controlled approaches using product temperature as an indication of endpoint rather than in-line moisture measurement. The resulting over-drying of the non-ADPC batches is a source of energy waste and possible attrition of the end-product material. Additionally, the ability to reliably fall within, but at the upper end, of a moisture specification helps to improve overall product yield.
Figure 4b (right) clearly demonstrates this variation with a much wider distribution of final LOD values evident for the non-ADPC controlled batches. The total spread of moisture content values is 0.48% for these batches, compared to only 0.16% for the ADPC-controlled batches, which demonstrate much tighter control. These results demonstrate the benefit of the in-line NIR moisture-content endpoint detection method.
Endpoint moisture content of the fluid bed granulation process is critical to final product quality and process performance and must be tightly controlled to avoid issues with downstream processing, product dissolution, and stability as well as drug absorption rates in the body. Implementing an ADPC approach can reduce batch-to-batch variation and improve batch repeatability and quality.
The ADPC-controlled approach to fluid bed granulation was shown to produce more consistently sized granules with less batch-to-batch variation when compared to granules produced from a non-ADPC controlled process. In addition, endpoint LOD analysis for the ADPC batches showed significantly less variation and greater consistency. Overall, high process repeatability and reproducibility were demonstrated across multiple, successfully manufactured fluid-bed granulation batches.
The real-time measurements of particle size and moisture content allowed the ADPC controller to effectively determine phase-end criteria. It was further shown to be possible to dynamically manage spray rate, thus ensuring a predetermined moisture content profile was followed by leveraging the NIR moisture-content data.
Finally, the addition of PAT and its integration into the process control strategy dramatically reduces the need for at-line sampling and testing associated with more traditional granulation approaches, as well as reducing the risks associated with human error.
Caroline McCormack is process laboratory manager; Chris O’Callaghan is head of engineering, firstname.lastname@example.org; and Gareth Clarke is Multieye Product Manager, all at Innopharma Technology, Dublin, Ireland. Prof. Ian Jones, PhD, is CEO of Innopharma and Innopharma Education, Dublin, Ireland; Luke Kiernan is a PhD student at the Technological University Dublin in Ireland; and Gavin Walker, PhD, is professor and director of the Synthesis and Solid State Pharmaceutical Centre at the University of Limerick in Ireland.
Vol. 44, No. 1
When referring to this article, please cite it as C. McCormack et al., “Self-Guided Control of a Fluid Bed Granulation Process," Pharmaceutical Technology 44 (1) 2020.