Title
Digital_Lyo

CoPED ID
98d8ad6f-f52b-4a53-af2c-a26c5e131d70

Status
Active


Value
£4,992,320

Start Date
June 30, 2023

End Date
June 30, 2025

Description

More Like This


The number of biopharmaceutical injectable products continues to increase. Predictions are that 40 per cent of new molecular entities will require batch freeze-drying for stability. The freeze-drying process (lyophilization) removes water from sensitive or high-value products such as vaccines, biologics, antibiotics, to extend shelf-life without the need for refrigeration/cold-chain. Freeze-drying processes need to be sustainable and commercially viable. There is a need to accelerate batch throughput and build capacity to increase efficiency and enable timely response to unexpected demand (e.g. COVID-19). Shortening drying times reduces energy demands and emissions and improves efficiency so lowering end-product costs. This aligns with the Clean Growth Strategy.

A pharmaceutical product development programme involves optimisation of formulations and processes for product viability and consistency; but product quality issues are identified at the end of a long cycle and at this stage significant costs have already been incurred. In-situ rapid analytical monitoring, giving real-time automated data, will provide feedback on and enable control of the lengthy freeze-drying process. Such insight can enable shortening of development times, reduced repeat runs and product failure/loss, lessened environmental costs and bioburden and ultimately improved product quality and consistency.

Freeze-drying employs high-global warming potential (GWP) refrigerants (banned 2030) or liquid nitrogen (high energy use in manufacture) for cooling, and improving sustainability requires a fresh approach. Implementation of a continuous freeze-drying Peltier system would be capable of a step change reduction in emissions. Further, freeze-drying processes must be repurposed for the expected increase in personalised medicines and the smaller batch runs and 'just-in-time' production schedules that this involves.

By building a consortium encompassing diverse expertise in key areas we have identified multiplexed Process Analytical Technology (PAT) to provide the required rapid data for modelling the freeze-drying process. Such coupled PAT sensor technology will enable scrutiny and control of batch freeze-drying and enable future continuous freeze-drying processes. Anticipated CO2 savings are in the order of 700 tonnes per newly developed product, achieved by reduced development cycles and increased production efficiencies in the order of 1 per cent. This is equivalent to savings of CO2 emissions of 300 tonnes per year per freeze-dryer.

This innovative multiplexed approach offers insight potential for in-depth analysis of factors impacting batch manufacturing freeze-drying efficiency. It further affords the opportunity to enhance process understanding of the freezing and drying stages to de-risk the deployment of new continuous manufacturing techniques, and ultimately maximise their efficiency and sustainability.

Neil Johnson PM_PER

Subjects by relevance
  1. Processes
  2. Production
  3. Products
  4. Product development
  5. COVID-19
  6. Drying
  7. Medicines
  8. Quality control
  9. Self-evaluation
  10. Optimisation
  11. Organisations (systems)
  12. Enterprises
  13. Development (active)
  14. Quality management
  15. Biopharmaceuticals

Extracted key phrases
  1. Biopharmaceutical injectable product
  2. Pharmaceutical product development programme
  3. Batch freeze
  4. Product quality issue
  5. Product cost
  6. Future continuous freeze
  7. Value product
  8. Product viability
  9. Product failure
  10. Lengthy freeze
  11. Process understanding
  12. Small batch run
  13. Increase
  14. New continuous manufacturing technique
  15. Batch throughput

Related Pages

UKRI project entry

UK Project Locations