A repeatable biofilm removal assay and its application in the assessment of commercial cleaning formulations for medical devices
Timothy S. CharltonUNSW Analytical Centre, University of New South Wales, NSW 2052, Australia. Email: tcharlton@aquafirma.com.au
Healthcare Infection 13(4) 131-135 https://doi.org/10.1071/HI08030
Published: 5 December 2008
Abstract
Bacterial biofilms are an important target of cleaning protocols for reusable medical devices. One approach to assess the efficacy of chemical cleaning formulations against this challenging type of soil is to grow biofilm of a specific strain on test coupons and measure the amount of biofilm removed after coupons have been immersed in a cleaning solution or control solution. This study reports on a comparison of four commercial formulations and two defined solutions in a biofilm removal assay. Biofilms of Pseudomonas aeruginosa (ATCC 25619) were grown on polytetrafluoroethylene coupons in a stirred reactor. A crystal violet assay was used to measure percent reduction of biofilm from test coupons by four commercial formulations and two defined solutions (sodium hydroxide and Tween 20). There was a significant pair-wise difference between all treatments (P < 0.05), other than one of the commercial formulations (3M RMEC 70505) and sodium hydroxide. A high level of repeatability was achieved with coefficients of variation from 1 to 19% for the different treatments. The repeatability of this method may allow an objective assessment of biofilm removal efficacy of commercial formulations used for cleaning medical devices.
Acknowledgements
The author wishes to thank M. Kritzler (Novapharm Research Australia Pty Ltd) for laboratory support and Dr Mick O’Neill (Statistical Advisory and Training Service Pty Ltd) for statistical analysis.
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