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OtherPDA Paper

Single-Use System Integrity IV: A Holistic Approach Based on Compiled Scientific Study Data

Marc Hogreve
PDA Journal of Pharmaceutical Science and Technology December 2022, pdajpst.2022.012794; DOI: https://doi.org/10.5731/pdajpst.2022.012794
Marc Hogreve
Sartorius
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Abstract

This concluding article of the publication series provides an overarching summary of all study results presented in the three previous articles [1, 2, 3]. Their interdependency in achieving a holistic approach to the integrity assurance of single-use systems (SUS) employed in (bio)pharmaceutical manufacturing is finally illustrated. Two of those three studies were conducted to understand microbial ingress and liquid leak mechanisms in polymeric film material as determinants of the maximum allowable leakage limit (MALL) for SUS using artificially created defects. The third study characterized gas flow through these defects – an essential variable for robust validation of physical integrity test methodologies based on gas flow. In all studies, the test samples used were 50 mm round patches of two ethylene vinyl acetate (EVA) multilayer films (300 μm and 360 μm thick) and a polyethylene (PE) multilayer film (400 μm thick). More than 1400 test samples with artificially created leaks were used in sizes ranging from 1 μm to 130 μm. The leaks were laser-drilled into the center of each patch. Microbial ingress and liquid leak testing under various process conditions resulted in a MALL of 2 μm for microbial integrity and the prevention of liquid leakages under most severe use-case conditions. The studies also demonstrated a close relationship between the occurrence of liquid leakage and microbial contamination. Different model solutions were used to evaluate the impact of liquid characteristics, mainly surface tension. The data were applied to build mathematical models for predicting the MALL under any use-case condition. By characterizing gas flow behavior over a broad pressure range using various defect sizes, it was possible to create formulas for three different flow regimes. These were suitable for calculating leak size in a defective product directly from the corresponding flow rate or vice versa. Finally, compilation of these different aspects enabled the authors to design and validate non-destructive physical integrity test methods having detection limits correlated to the MALL for SUS.

  • Single-use system (SUS)
  • gas flow rate through microchannels
  • liquid leak testing
  • maximum allowable leakage limit (MALL)
  • microbial ingress testing
  • single-use system integrity (SUSI)
  • Received August 24, 2022.
  • Accepted December 14, 2022.
  • Copyright © 2022, Parenteral Drug Association
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PDA Journal of Pharmaceutical Science and Technology: 79 (1)
PDA Journal of Pharmaceutical Science and Technology
Vol. 79, Issue 1
January/February 2025
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Single-Use System Integrity IV: A Holistic Approach Based on Compiled Scientific Study Data
Marc Hogreve
PDA Journal of Pharmaceutical Science and Technology Dec 2022, pdajpst.2022.012794; DOI: 10.5731/pdajpst.2022.012794

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Single-Use System Integrity IV: A Holistic Approach Based on Compiled Scientific Study Data
Marc Hogreve
PDA Journal of Pharmaceutical Science and Technology Dec 2022, pdajpst.2022.012794; DOI: 10.5731/pdajpst.2022.012794
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Keywords

  • Single-use system (SUS)
  • gas flow rate through microchannels
  • liquid leak testing
  • maximum allowable leakage limit (MALL)
  • microbial ingress testing
  • single-use system integrity (SUSI)

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