Case study: Antibody drug conjugates containment suite

Published: 13-Aug-2024

Howorth Air Technology discusses how it overcame the key containment challenges associated with the development of Highly Potent Active Pharmaceutical Ingredients (HPAPI) compounds

UK-based Howorth Air Technology discusses how it overcame the key challenges associated with the turnkey responsibility of six containment suites designed with an OEL of 1ng/m3.

The challenge

There is an increasing demand for HPAPIs due to their effectiveness against cancer at lower doses and the trend towards more targeted therapeutics.

The next generation of ADC (Antibody Drug Conjugates) development requires more complex technology including specialist containment systems to handle the Highly Potent Active Pharmaceutical Ingredients (HPAPI) during dispensing and lyophilisation phases when the cytotoxins are at their greatest hazard.

The facility expansion doubles production of the most highly potent active pharmaceutical ingredients

Increasing capacity at this state-of-the-art CDMO facility required significant expansion to enable contained handling of high-potency small-molecule organic synthesis including key design and integration of key process equipment ensuring “total containment” was achieved throughout.

The solution

Howorth was selected based on proven experience providing task-based containment solutions for highly potent compounds.

The scope of the project included full turnkey responsibility of 6 x containment suites designed with an OEL of 1ng/m3 (task-based).

The scope of the project included full turnkey responsibility of 6 x containment suites designed with an OEL of 1ng/m3 (task-based)

Multi-collaboration across key customer stakeholders and process equipment suppliers was identified from the outset as key to the success of the project which was implemented expertly by Howorth delivery team with an additional challenge of moving into our new pharma facility at Raven Locks!

The final solution included extensive, integrated, multi-operation isolator technology to maintain full containment through the entire API synthesis, purification, and isolation steps including:

  • Multi-chamber preparation isolator including weighing equipment, operator platform, rapid transfer ports and “thro-wall” powder transfer connection to reactors
  • Walk-in hood/kilo booth including integration of glass reactor and chromotography systems
  • RotoVap Isolator including supply and integration of 1 x RotoVap system
  • Wash/transfer isolator to clean the RotoVap flasks prior to removal/replacement
  • Process isolator including supply and integration of 1 x vacuum tray oven and 1 x lyopholiser

The scope of the project included full turnkey responsibility of 6 x containment suites designed with an OEL of 1ng/m3 (task based).

The scope of the project included full turnkey responsibility of 6 x containment suites designed with an OEL of 1ng/m3 (task based).

The outcome

The facility expansion doubles production of the most highly potent active pharmaceutical ingredients, is fully validated to GMP standards, and is certified by specialist occupational and environmental toxicologists.

The facility is designed to follow the most stringent criteria for highly active compound manufacturing and engineered for containment and isolation of potent compounds providing the customer with the flexibility demanded by the Pharmaceutical customers.

 

Top image: Howorth Ar Technology - High Containment Facility 

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