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Research ArticleTechnology/Application

Container/Closure Integrity Testing and the Identification of a Suitable Vial/Stopper Combination for Low-Temperature Storage at −80 °C

Brigitte Zuleger, Uwe Werner, Alexander Kort, Rene Glowienka, Engelbert Wehnes and Derek Duncan
PDA Journal of Pharmaceutical Science and Technology September 2012, 66 (5) 453-465; DOI: https://doi.org/10.5731/pdajpst.2012.00884
Brigitte Zuleger
1Bavarian Nordic GmbH, Robert Roessle Strasse 10, D-13125 Berlin, Germany;
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Uwe Werner
1Bavarian Nordic GmbH, Robert Roessle Strasse 10, D-13125 Berlin, Germany;
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Alexander Kort
2IDT Biologika GmbH, Am Pharmapark, D-06861 Dessau-Rosslau, Germany; and
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Rene Glowienka
2IDT Biologika GmbH, Am Pharmapark, D-06861 Dessau-Rosslau, Germany; and
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Engelbert Wehnes
1Bavarian Nordic GmbH, Robert Roessle Strasse 10, D-13125 Berlin, Germany;
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Derek Duncan
3Lighthouse Instruments, Science Park 406, NL-1098 XH Amsterdam, The Netherlands
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Abstract

It was recently found that after storage of a live viral vaccine at −80 °C in glass vials closed with rubber stoppers, a phenomenon was revealed which had not been observed before with other viral products stored at −20 °C: overpressure in the vials. As this phenomenon poses a serious safety problem for medical personnel as well as for the product itself, an investigation was initiated to identify the root cause of the overpressure. After exclusion of possible root causes (differences in air temperature or atmospheric air pressure during filling and quality control testing, outgassing from the formulation buffer) the remaining hypothesis involved a possible container closure integrity issue at low temperature. The glass transition temperatures (Tg) of many rubber stopper formulations are in the range −55 to −70 °C. At storage temperatures below Tg, the rubber stopper loses its elastic properties and there is a risk that the seal integrity of the vial could be compromised. Loss of seal integrity of the vials near storage temperatures of −80 °C would result in an ingress of cold dense gas into the vial headspace. After removal of the vials from storage at −80 °C, the rubber stoppers could regain their elastic properties and the vials would quickly reseal, thereby trapping the ingressed gas, which leads to overpressure in the vial headspace. Nondestructive laser-based headspace analysis was used to investigate the maintenance of container closure integrity as a function of the filling and capping/crimping process, storage and transport conditions, and vial/stopper designs. This analytical method is based on frequency modulation spectroscopy (FMS) and can be used for noninvasive headspace measurements of headspace pressure and headspace gas composition. Changes in the vial headspace composition and/or pressure are a clear marker for vials that have lost container closure integrity.

LAY ABSTRACT: After storage of a live viral vaccine at −80 °C in glass vials closed with rubber stoppers, overpressure in some of the vials was observed, posing a serious safety problem for medical personnel as well as for the product. A working hypothesis to explain this phenomenon involved a possible container closure integrity issue at these low temperatures. The glass transition temperatures (Tg) of many rubber stopper formulations are in the range −55 to −70 °C. At storage temperatures below Tg, the rubber stopper loses its elastic properties, resulting in compromised seal integrity of the vial and ingress of cold dense gas into the vial headspace. Upon thawing, the rubber stoppers regain their elastic properties and the vials quickly reseal, thereby trapping the ingressed gas, which leads to overpressure in the vial headspace. Nondestructive, laser-based headspace analysis, which is able to detect changes in headspace pressure and gas composition, was used to investigate the maintenance of container closure integrity. Changes in the vial headspace composition and/or pressure are a clear marker for vials that have lost container closure integrity.

  • Storage at −80 °C
  • Live viral vaccines
  • Container closure integrity
  • Headspace analysis
  • Frequency modulation spectroscopy
  • Glass transition temperature
  • © PDA, Inc. 2012
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PDA Journal of Pharmaceutical Science and Technology: 66 (5)
PDA Journal of Pharmaceutical Science and Technology
Vol. 66, Issue 5
September/October 2012
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Container/Closure Integrity Testing and the Identification of a Suitable Vial/Stopper Combination for Low-Temperature Storage at −80 °C
Brigitte Zuleger, Uwe Werner, Alexander Kort, Rene Glowienka, Engelbert Wehnes, Derek Duncan
PDA Journal of Pharmaceutical Science and Technology Sep 2012, 66 (5) 453-465; DOI: 10.5731/pdajpst.2012.00884

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Container/Closure Integrity Testing and the Identification of a Suitable Vial/Stopper Combination for Low-Temperature Storage at −80 °C
Brigitte Zuleger, Uwe Werner, Alexander Kort, Rene Glowienka, Engelbert Wehnes, Derek Duncan
PDA Journal of Pharmaceutical Science and Technology Sep 2012, 66 (5) 453-465; DOI: 10.5731/pdajpst.2012.00884
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More in this TOC Section

  • Mechanical Container Closure Integrity Test: A Method for Cartridge Systems
  • A Container Closure Integrity Test Method for Vials Stored at Cryogenic Conditions Using Headspace Oxygen Analysis
  • Best Practices for Microbial Challenge In-Use Studies to Evaluate the Microbial Growth Potential of Parenteral Biological Products; Industry and Regulatory Considerations
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Keywords

  • Storage at −80 °C
  • Live viral vaccines
  • Container closure integrity
  • headspace analysis
  • Frequency modulation spectroscopy
  • Glass transition temperature

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