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Comparison of European and US biological indicators for ethylene oxide sterilization
Authors:Christopher A Demitrius  Anthony P Duran  Virginia C Chamberlain  Victoria M Hitchins
Institution:(1) Midwest Laboratory for Microbiological Investigations, US Food and Drug Administration, 55401 Minneapolis, MN, USA;(2) Center for Devices and Radiological Health, US Food and Drug Administration, 5600 Fishers Lane, 20857 Rockville, MD, USA
Abstract:Summary Biological indicators (BIs) are used to monitor ethylene oxide (EO) gas sterilization processes for medical devices. Several European and United States BIs for EO sterilization were evaluated for resistance according to both United States Pharmacopeia (USP) XXI and United Kingdom's (UK) tests for D-values. US BIs areB. subtilis var. niger spores on paper strips or disc carriers while European BIs use aluminum strips, quartz sand, or cotton yarn. Numerous BIs per run and runs per lot, as well as 2–3 different lots of BIs from each manufacturer, were examined. Both British and US BIs met their respective label claims for rates of inactivation when tested against British and USP EO test parameters, respectively. However, Danish BIs, on cotton yarn or quartz sand, were not inactivated following USP specifications during the exposure dwell times tested (600 mg L–1 EO, 54°C, 60% RH, 0–110 min). The Danish BIs will require further testing in order for us to determine if theirB. subtilis spores are unusually resistant to EO or if the spore carrier substrates protect the spores from the sterilizing gas. In conclusion, the British and American BIs for EO sterilization are equivalent in resistance despite differences in carrier substrate, recovery conditions, calculation methods for D-values, and the labeled sterilization conditions for use.
Keywords:Biological indicators  Ethylene oxide  Medical devices  International standards
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