Journal
ANTIMICROBIAL RESISTANCE AND INFECTION CONTROL
Volume 6, Issue -, Pages -Publisher
BIOMED CENTRAL LTD
DOI: 10.1186/s13756-017-0271-3
Keywords
Peracetic acid; Virucidal efficacy; Instrument disinfection
Categories
Funding
- Chemische Fabrik Dr. Weigert GmbH & Co. KG, Germany
- Helmholtz Centre for Infection Research, Hannover Germany
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Background: Various peracetic-acid (PAA)-based products for processing flexible endoscopes on the market are often based on a two-component system including a cleaning step before the addition of PAA as disinfectant. The peracetic acid concentrations in these formulations from different manufacturers are ranging from 400 to 1500 ppm (part per million). These products are used at temperatures between 20 degrees C and 37 degrees C. Since information on the virus-inactivating properties of peracetic acid at different concentrations and temperature is missing, it was the aim of the study to evaluate peracetic acid solutions against test viruses using the quantitative suspension test, EN 14476. In addition, further studies were performed with the recently established European pre norm (prEN 17111: 2017) describing a carrier assay for simulating practical conditions using frosted glass. Methods: In the first step of examination, different PAA solutions between 400 and 1500 ppm were tested at 20 degrees C,25 degrees C, and 35 degrees C with three test viruses (adenovirus, murine norovirus and poliovirus) necessary for creating a virucidal action according to the European Norm, EN 14476. A second step for simulating practical conditions based on prEN 17111: 2017 followed by spreading a test virus together with soil load onto a glass carrier which was immerged into a peracetic acid solution. A fixed exposure time of five minutes was used in all experiments. Results: In the quantitative suspension test 1500 ppm PAA solution was needed at 35 degrees C for five minutes for the inactivation of poliovirus, whereas only 400 ppm at 20 degrees C for adeno-and murine norovirus were necessary. In the carrier assay 400 ppm peracetic acid at 20 degrees C were sufficient for adenovirus inactivation, whereas 600 ppm PAA were needed at 25 degrees C and 35 degrees C and 1000 ppm at 20 degrees C for murine norovirus. A PAA solution with 1000 ppm at 35 degrees C was required for complete inactivation of poliovirus. However, a dramatically decrease of titer after the drying and immerging could be observed. In consequence, a four log reduction of poliovirus titer could not be achieved in the carrier test. Conclusion: In summary, 1500 ppm PAA at 35 degrees C was necessary for a virucidal action in the quantitative suspension test. After passing the requirements of the suspension test, additional examinations with adeno-and murine norovirus on glass carriers based on prEN 17111: 2017 will not additionally contribute to the final claim of an instrument disinfectant for virucidal efficacy. This is due to the great stability of poliovirus in the preceded quantitative suspension test and the fact that poliovirus could not serve as test virus in the following carrier assay.
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