De-risking excipient particle size distribution variability with automated robust mixing: Integrating quality by design and process analytical technology
Particle size distribution (PSD) variability in excipients affects mixing. In response, manufacturers rely on raw material control and rigidly defined process parameters to achieve quality. However, this status quo is costly; and diverges from regulatory exceptions for process robustness. Although robustness improves cost and material usage efficiency, it remains under-adopted.
Highlights
Particle size distribution (PSD) changes in lactose powder cause over- & under-mixing.
Automated robust mixing operation designed to achieve quality-defined mixing.
NIR used to characterize PSD & blend homogeneity for feedforward & feedback control.
Mitigated effects of PSD variability and reduced mixing time (13–34%)
End-to-end implementation of PAT framework with synTQ FM achieved.
Method
To address this gap, a robust batch mixing operation that mitigated the impact of PSD variability was evaluated, with blends comprising chlorpheniramine, microcrystalline cellulose and lactose. PSD of lactose was varied to simulate commercially-relevant variability. Due to PSD-induced rheological variations, the blends had different optimal mixing speeds. For the automation study, near infrared (NIR) spectroscopy; process optimization and endpoint detection algorithms; and control hardware were integrated within a cluster of software environments. NIR spectroscopy was employed for in-line PSD characterization and blend monitoring, to modulate mixing speed and detect endpoint (feedforward and feedback control).
Results
NIR spectroscopy rapidly detected PSD variations by the 6th–9th rotations, to activate feedforward control, which mitigated the effect of PSD variability and reduced the mixing time by 13–34%. Endpoints were correctly detected. PSD variations and blend homogeneity were accurately predicted (relative standard error of prediction ≤ 2%).
Conclusion
The automated robust mixing operation was successful. Pertinently, NIR spectrometer can be adopted for multimodal sensing. Its applicability for production-driven characterization of raw materials in batch and continuous pharmaceutical processing should be further explored. Lastly, this study laid the groundwork for end-to-end implementation of process analytical technology in robust batch processing. Continue on De-risking excipient particle size distribution variability with automated robust mixing: Integrating quality by design and process analytical technology
Author links open overlay panelWee Beng Lee, Effendi Widjaja, Paul Wan Sia Heng, LaiWah Chan
European Journal of Pharmaceutics and Biopharmaceutics
Available online 3 October 2020