Article

Vaporized Hydrogen Peroxide (VHP): A Well-Known Technology with a New Application

This paper examines how to overcome the challenges using Vaporized Hydrogen Peroxide (VHP) in end of production line sterilization.
July 20, 2021

Key Takeaways:

  • Vaporized hydrogen peroxide (VHP) is a proven sterilant with strong oxidizing power, effective against a wide range of microorganisms and compatible with many materials.
  • Recent innovations in chamber design and process control are expanding VHP’s potential for terminal sterilization of single-use medical devices.
  • Material and packaging compatibility are key limitations, requiring careful selection of non-absorptive, permeable materials to ensure sterilant penetration.
  • VHP sterilization cycles involve preconditioning, exposure and aeration, with critical control of humidity, pressure and sterilant concentration to ensure efficacy.
  • Global standards for VHP sterilization are under development, aiming to provide regulatory clarity and support broader adoption in healthcare and manufacturing. 
Hydrogen peroxide has a multitude of uses and the vapor form was first identified as a sterilant in late 1970s. Following a number of developments, vaporized hydrogen peroxide (VHP) became widely adopted in early 90s as a substitute for ethylene oxide (EO) in device and instrument processing and reprocessing in healthcare facilities. Often VHP was hailed as the replacement technology for EO. Because of key limitations such as scale, penetration, and compatibility with packaging materials, adoption to terminal sterilization of single-use devices has not commenced to any significant level. However, recent developments in sterilization chamber design and process development provide new opportunity for consideration. For future products, such as those that require “end of production line sterilization,” such limitations may be reconsidered and overcome. This article describes those challenges and how they have been addressed with practical examples.

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