Antimicrobial Evaluation of a Surface Protector System
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Duong (2016) Antimicrobial Evaluation of a Surface Protector System Andrew Duong Edited by: Michael Diamond Reviewed by: Dr. Uyen Nguyen Disclaimer: The authors of this report and InfectionControl.tips declare no conflict of interest with the following critical evaluation and research. No funds or influence were provided to the authors or InfectionControl.tips by any parties. Abstract: The spread of hospital acquired infections has been spurned by the overuse of antibiotics and the challenges of hospital cleaning. In this study, the effectiveness of an antimicrobial surface protector was evaluated. Following exposure to the Clean2Touch surface protector, it was shown that the protector was effective in reducing the growth of Staphylococcus aureus,Clostridium difficile, Escherichia coli, and methicillin-resistant S. aureus.After 2 h of incubation on the surface, there was a significant reduction in the number of viable microorganisms. Interestingly, the experiments demonstrated that a large majority of bacteria were killed instantaneously upon exposure to the antimicrobial film. Introduction: hospital visit [3]. In The World Health Organization has immunocompromised patients, this published numerous documents on presents a serious and sometimes the rising threat of antimicrobial lethal threat. resistance and its impact on the future global health [5]. Much of this Hospitals use a variety of detergents resistance is driven by the and cleansers to clean rooms in widespread and irresponsible use of between patients. However, it antibiotics to treat patients when they requires vigilant employees to do not have a bacterial infection. The ensure that the standard operating overuse of antibiotics resulted in the procedures are followed and regular development and subsequent spread maintenance to remain effective in of drug-resistant, and more minimizing the bacterial population dangerously, multi-drug resistant (bioburden) [3,9]. Due to economic bacteria [4, 7]. These new strains of reasons, employee vigilance is least pathogens often cause hospital- emphasized by hospital acquired infections (HAIs), which is administrators because it is a costly an infection that occurs following a task [9]. One alternative is to 1 InfectionControl.tips www.IC.tips (2016) 8, 1-6 Duong (2016) maintain a low bioburden on The number of microorganisms was surfaces through the application of tested initially by removing a 50 × 50 antimicrobial surface mm square of the sample and coatings. Some systems use placing it in 10 ml tryptone soy broth. mechanical methods to maintain low This solution was then agitated to bacterial populations. Mechanical liberate the bacteria. One millilitre of methods reduce the bioburden broth was inoculated onto TSA blood without propagating antibiotic agar and cultured at 35˚C (40˚C resistance or chemical tolerance as for C. difficile) for 48 h. The number opposed to chemical or antibiotic- of CFU was evaluated at this stage. based solutions. In this study, we evaluate the effectiveness of a To determine the bacteriocidal mechanical antimicrobial surface activity of the culture during short protector, Clean2Touch, in the term incubation, a similar procedure reduction of bacteria on surfaces. was followed. E. coli and S. aureus cultures (1.9 × 106 CFU/mL Methods: and 1.9 × 106 CFU/mL, respectively) All experiments were performed by a were inoculated onto a petri dish third party laboratory. containing a 20 × 20 mm sterile sample with or without Clean2Touch To evaluate the microbial load film. A second, untreated piece of following exposure to “Clean2Touch” sterile film was placed on top of the system, 0.4 mL of each microbial liquid to reduce evaporation and to sample (Clostridium ensure a uniform spread of the difficile, methicillin-resistant bacterial culture. Samples were Staphylococcus aureus, Escherichia incubated for 2, 4, or 6 h. Following coli, and Staphylococcus aureus) at incubation, the upper film was a concentration of 2.5 ×105 colony removed, and the bacteria were forming units per millilitre (CFU/mL) irrigated from the sample using 10 were inoculated onto sample slides mL of phosphate buffered saline. with or without the treated The number of colonies in each protector. A sterile piece of plastic sample was determined from this was placed over each inoculum to suspension. ensure even distribution of the culture. All samples, except C. Results: difficile, were incubated at 35˚C for Growth of bacterial cultures on the 24h. C. difficile was incubated at antimicrobial film was found to be 40˚C for 24 h. Controls at time zero extremely limited compared to the (prior to incubation) were evaluated control samples without film after a for the presence of microorganisms 24 h exposure period (Table 1). In in addition to the 24 h samples. samples without the film, it should be noted that all microorganisms 2 InfectionControl.tips www.IC.tips (2016) 8, 1-6 Duong (2016) increased in quantity, despite the untreated samples, the decrease lack of a growth substrate on the was highly significant when the testing surface. Growth increased bacteria were inoculated onto the from a modest 33.3% (MRSA), up to treated surface. The original an increase of 113.3% (S. concentration decreased from 2.5 × aureus). There was a reduction in 105 CFU/mL to an average of 2.4 × the number of bacteria on the 102 CFU/mL on the treated sample, samples containing Clean2Touch but actually increased from the same film. Reduction of the original original concentration to an average inoculum ranged from 86.7% (S. concentration of 9.3 × 105CFU/mL on aureus) to 91.4% (MRSA). the untreated samples. One interesting observation was the A similar experiment was performed immediate reduction in bioburden evaluating a shorter, more realistic upon inoculation onto the exposure period. Only E. coli and S. Clean2Touch film (Table 1, 0 aureus were evaluated. However, H). Although there was an the results can be extrapolated to immediate decrease in the number of other microorganisms based on viable microorganisms following previous experiments. In this set of inoculation of the bacteria onto experiments, after a 2 h exposure Table 1. Number of viable microorganisms following culture on treated and untreated surfaces 3 InfectionControl.tips www.IC.tips (2016) 8, 1-6 Duong (2016) time, the majority of E. coli and S. Discussion: aureus were killed by the The Clean2Touch antimicrobial film antimicrobial film. After 2 h, the reduced the number of bacteria bioburden of E. coli was reduced by following exposure. After 24 h of 3.4 log (Figure 1). After 6 h, this was incubation of bacteria on the film, only increased to a 4.0-fold log there was a marked decrease in reduction from the original bioburden, especially for methicillin- inoculum. A similar trend was resistant S. aureus. The same trend observed for S. aureus. After 2 h, was observed when monitoring the there was a 3.3-fold log reduction in number of viable bacteria with the number of viable S. shorter exposure time. A 3-fold log aureus. However, there was >6.1- (1000×) reduction in S. fold log reduction just after 4 hours aureus species was observed after 2 (Figure 2). The reduction inS. h exposure time and this was aureus on the surface without increased to >6.1-fold log reduction antimicrobial film only exhibited a after 6 h exposure. modest 0.6-fold log reduction after 2 h and a 1.1-fold log reduction after 6 HAIs target most patients, but h (Figure 2). especially the young, elderly, and Figure 1: Antibacterial activity of Clean2Touch Surface Protector Against E. coli 4 InfectionControl.tips www.IC.tips (2016) 8, 1-6 Duong (2016) Figure 2: Antibacterial activity of Clean2Touch Surface Protector Against S. aureus immune-compromised patients. testing compared to MRSA. There are minimal differences between Although most pathogens are these two strains, as antibiotic capable of causing HAI’s, certain resistance is conferred by small species have been implicated in changes in the bacterial cell wall. outbreaks [3]. The initial [1,8] experiments evaluated S. aureus, E. coli, C. difficile, and methicillin- The almost immediate reduction in resistant S. aureus because these the number of viable bacteria pathogens are considered a following inoculation on the significant source of HAIs [2, 6]. The antimicrobial film provided evidence Clean2Touch antimicrobial film was that the film has bactericidal found to be effective at eliminating all properties (Figures 1 and 2). There four species. It was especially was an immediate average 3.95-fold effective at reducing MRSA after 24 log reduction in the number of viable h and S. aureus after 4 h. Only S. bacteria. These values are very aureus viability was monitored at similar to the bioburden reduction shorter time periods following observed after 2 h, which suggests exposure to the antimicrobial that an extremely limited exposure film. This was largely in part due to time to the antimicrobial film may be the availability of S. aureus for effective for the reduction of pathogens to a safe level. 5 InfectionControl.tips www.IC.tips (2016) 8, 1-6 Duong (2016) Conclusion: The Clean2Touch antimicrobial film hospitals and other public spaces greatly reduced the number of viable with an innovative method for microorganisms exposed to the combating diseases without fueling film. The use of non-chemical the antimicrobial-resistance arms methods to eliminate the presence of race. pathogens on surfaces provides References: 1. Chambers HF. Methicillin-resistant Staphylococcus aureus. Mechanisms of resistance and implications for treatment. Postgraduate medicine. 2001 Feb;109(2 Suppl):43-50. 2. Dancer SJ. The role of environmental cleaning in the control of hospital- acquired infection. Journal of hospital Infection. 2009 Dec 31;73(4):378- 85. 3. Dancer SJ. Controlling hospital-acquired infection: focus on the role of the environment and new technologies for decontamination. Clinical microbiology reviews. 2014 Oct 1;27(4):665-90.