key: cord-0841081-lc1l9vp4
authors: Brêda Mascarenhas, Luís Alberto; Machado, Bruna Aparecida Souza; Rodrigues, Leticia de Alencar Pereira; Saraiva Hodel, Katharine Valéria; Bandeira Santos, Alex Álisson; Freitas Neves, Paulo Roberto; da Silva Andrade, Leone Peter Correia; Soares, Milena Botelho; de Andrade, Jailson Bittencourt; Badaró, Roberto
title: Potential application of novel technology developed for instant decontamination of personal protective equipment before the doffing step
date: 2021-06-04
journal: PLoS One
DOI: 10.1371/journal.pone.0250854
sha: 2b0715f76f84830a4df82143c6f53ef97ef60f0a
doc_id: 841081
cord_uid: lc1l9vp4

The use of personal protective equipment (PPE) has been considered the most effective way to avoid the contamination of healthcare workers by different microorganisms, including SARS-CoV-2. A spray disinfection technology (chamber) was developed, and its efficacy in instant decontamination of previously contaminated surfaces was evaluated in two exposure times. Seven test microorganisms were prepared and inoculated on the surface of seven types of PPE (respirator mask, face shield, shoe, glove, cap, safety glasses and lab coat). The tests were performed on previously contaminated PPE using a manikin with a motion device for exposure to the chamber with biocidal agent (sodium hypochlorite) for 10 and 30s. In 96.93% of the experimental conditions analyzed, the percentage reduction was >99% (the number of viable cells found on the surface ranged from 4.3x10(6) to <10 CFU/mL). The samples of E. faecalis collected from the glove showed the lowest percentages reduction, with 86.000 and 86.500% for exposure times of 10 and 30 s, respectively. The log(10) reduction values varied between 0.85 log(10) (E. faecalis at 30 s in glove surface) and 9.69 log(10) (E. coli at 10 and 30 s in lab coat surface). In general, E. coli, S. aureus, C. freundii, P. mirabilis, C. albicans and C. parapsilosis showed susceptibility to the biocidal agent under the tested conditions, with >99% reduction after 10 and 30s, while E. faecalis and P. aeruginosa showed a lower susceptibility. The 30s exposure time was more effective for the inactivation of the tested microorganisms. The results show that the spray disinfection technology has the potential for instant decontamination of PPE, which can contribute to an additional barrier for infection control of healthcare workers in the hospital environment.

>99% (the number of viable cells found on the surface ranged from 4.3x10 6 to <10 CFU/ mL). The samples of E. faecalis collected from the glove showed the lowest percentages reduction, with 86.000 and 86.500% for exposure times of 10 and 30 s, respectively. The log 10 reduction values varied between 0.85 log 10 (E. faecalis at 30 s in glove surface) and 9.69 log 10 (E. coli at 10 and 30 s in lab coat surface). In general, E. coli, S. aureus, C. freundii, P. mirabilis, C. albicans and C. parapsilosis showed susceptibility to the biocidal agent under the tested conditions, with >99% reduction after 10 and 30s, while E. faecalis and P. aeruginosa showed a lower susceptibility. The 30s exposure time was more effective for the inactivation of the tested microorganisms. The results show that the spray disinfection technology has the potential for instant decontamination of PPE, which can contribute to an additional barrier for infection control of healthcare workers in the hospital environment. a1111111111 a1111111111 a1111111111 a1111111111 a1111111111

Introduction and disinfection chambers [37] . Faced with increased production and demand, health regulatory agencies recommend that studies be presented to prove the performance of these devices in the face of decontamination effectiveness [38, 39] . Although there are few studies demonstrating the efficacy of disinfection chambers [40] , their use becomes interesting for the decontamination of surfaces, including personal protective closes and equipment (PPE), since it is not mandatory that the contaminated material undergoes to manual cleaning mainly at the moment before the doffing step for previous elimination of the microorganisms [37] . Thus, disinfection chambers can be a practical alternative for bioburden control in environments with a high rate of pathogenic microorganisms, such as hospitals. In addition, the disinfection chambers can help mitigate the possibility of an accident self-contamination of the HCWs during the processing of hand manipulation of the disposable PPEs.

Different disinfecting agents have been studied and suggested to act in these devices as biocidal agents against different pathogens of hospital importance (such SARS-CoV-2, multidrug-resistant bacteria and fungi). Examples include physical agents such as UV light [41] and chemical agents such as alcoholic solutions [5, 42] , quaternary ammonium compounds [43, 44] , ozone gas [45] and sodium hypochlorite [46] . Sodium hypochlorite is one of the most well-known and used biocidal agents worldwide due to its broad-spectrum microbicidal properties [47] . Compared with other chlorine-containing biocides, the use of sodium hypochlorite is characterized by a relatively lower toxicity when in contact with mucous membranes, the equipment required for its synthesis are simpler, its handling is safer, and its operation and preparation costs are lower, which makes its use feasible in hospitals [48] . In addition, the use of sodium hypochlorite is recommended by the World Health Organization (WHO) for the disinfection of environmental surfaces related to health care in the context of COVID-19, in concentrations between 0.1 and 0.5% (1000 and 5000 ppm, respectively) [49] .

Despite being a promising alternative, especially considering the current situation, there are still few reports in the literature on the efficacy of disinfection chambers and/or devices using sodium hypochlorite as a biocidal agent for reducing or inactivating the burden of different pathogens on contaminated surfaces, more specifically for PPE, and on its potential use in emergency and public health situations. [38, 50, 51] . The use of disinfection chambers in controlled environments, such as hospitals and health units, could help to reduce the risk of selfcontamination by health workers during the doffing step, since the instantaneously dispersed solution could significantly reduce the pathogens present on surfaces and contribute to greater safety of these HCWs self-contamination. Nevertheless, this approach has not yet been reported by any earlier study.

Through the use of the disinfection chamber it is possible to decontaminate the surfaces of all PPEs used in clinical practice at the same time, making the doffing step safer for the HCWs. This can be considered an advantage over the PPE disinfection technologies mentioned in the literature [52] [53] [54] , since the proposed decontamination processes do not reduce the risk of self-contamination. Indeed, the objective of this study was to develop a disinfection chamber for instantaneous dispersion of a biocidal solution (0.25% sodium hypochlorite) and to determine its efficacy on previously contaminated surfaces at different exposure times, aiming at its possible application as an additional barrier against pathogens, such as SARS-CoV-2, to protect HCWs during the withdraw procedure prior PPE disposal. Fig 1 shows the general scheme of the method applied in this study to evaluate the efficacy of the chamber for instant disinfection of the surfaces of seven PPE previously contaminated with different microorganisms and subjected to different exposure times to the biocidal agent (0.25% sodium hypochlorite). To evaluate the efficacy of the disinfection process, tests were performed in two distinct steps with quantitative and qualitative analyses using a manikin that moved through a linear and rotary motion system to simulate the passage of an individual in a hospital environment (before the doffing step), an environment well known for presenting a high burden of infectious agents [55] .

The chamber consisted of a modular framework constructed of aluminum and carbon steel, with dimensions of 240 x 150 x 250 cm (height x depth x width), with an open entrance and exit. The design of the disinfection chamber allows the framework to be easily transported, installed and uninstalled. The nebulization system for the chamber comprised six nebulizer nozzles (Senninger, USA) installed on the inner side and top of the chamber to promote a better homogeneity in the spraying of the biocide agent. In addition, a water filter, a submerged pump and a 1-m 3 storage tank (1000 L capacity) with lid, with flow rate of 10 L/h were used to complete the system. The command and control system was installed by means of an electrical panel with voltage of 220 V, was responsible for the activation and operation of the entire system and contained a sensor for the activation of the nebulizers.

The biocidal agent (bleach) was prepared at a concentration of 0.25% [49, 56] by diluting an initial solution with 2.38% active chlorine [57] . A total volume of 1,000 L was prepared directly in the storage tank of the chamber for the experiments. All experiments to evaluate the disinfection potential of PPE were performed during the first three days after preparation of the biocidal agent (bleach). The stability of the biocidal agent (0.25% sodium hypochlorite) was evaluated on days 0, 3, 6, 9, 13 and 20 by determining the percentage of active chlorine present in the solution and through pH analysis. The use of the biocide agent in the concentration of 0.25% was based on the WHO recommendation for the disinfection of environmental surfaces, which ranges from 0.1 to 0.5% [49] . Thus, an intermediate concentration was chosen. The amount of active chlorine was evaluated by iodometric titration [58] , and the pH was determined through the hydrogen ionic activity using a standard electrode (pH meter, Mettler-Toledo). The analyses were performed in triplicates. 

The standard reference strains used in this study were Escherichia coli (ATCC 8739), Staphylococcus aureus (ATCC 6538), Pseudomonas aeruginosa (ATCC 27853), Enterococcus faecalis (ATCC 29212), Citrobacter freundii (ATCC 43864), Proteus mirabilis (ATCC 29906), Candida albicans (ATCC 18804) and Candida parapsilosis (ATCC 22019), which were obtained from Microbiologics (St. Cloud, Minnesota) or from the Culture Collection of the Institute of Health Sciences, Federal University of Bahia (Universidade Federal da Bahia-UFBA), located in Salvador, Brazil. The selection of test strains was based on studies of microorganisms commonly causing nosocomial infections, as well as on the recommendations of regulatory agencies for evaluating the efficacy of chemical disinfectants [57, [59] [60] [61] [62] [63] [64] [65] . The suspensions of the test microorganisms were prepared by transferring cells from the pure culture to plates containing 15-20 mL of plate count agar: agar (9 g/L); dextrose (1 g/L); tryptone (5.0 g/L) and yeast extract (2.5 g/L). To evaluate the disinfection profile in the chamber against the test microorganisms, the inocula were prepared by suspending 1-5 colonies in 5 mL of 0.85% saline solution and the turbidity was adjusted to McFarland No. 0.5 tube [66] .

The PPE items used to evaluate the effectiveness of the disinfection chamber were selected according to the recommendations for prevention and control of the spread of SARS-CoV-2 and other infectious agents transmitted mainly by aerosols in health services (Table 1) [24, 67, 68] . To ensure the sterility of the surface of the selected items before contamination with the standard strains, the items were exposed to UV light for 40 minutes using a laminar flow (model LA2000T, LOGEN) after being sanitized with 70% ethanol [69] . Surface samples from each item were collected using sterile swabs, and their contents were seeded in nutrient agar (37˚C for 24 hours) to confirm sterility.

The assays for evaluating the disinfection potential of the biocidal agent in the chamber developed in this study were based on the method used to monitor viable particles on surfaces [70, 71] and qualitative analysis of the biocidal agent distribution on the surfaces [72] . The disinfection process was performed by spraying the biocidal agent (0.25% sodium hypochlorite) in the chamber using a suitably dressed manikin with a motion system that allowed the manikin to pass through the chamber automatically and to perform a 360˚turn, for 10 and 30 s of exposure. The manikin was chosen so that there would be a simulation closer to what would be the use of the disinfection chamber by healthcare workers in nosocomial environment. In the first [70] were used for contamination, with the right side used for the control (without exposure to the biocidal agent by spraying, in other words, these surfaces were sampled before the manikin (and PPE) was decontaminated) and the left side used for each test microorganism (Fig 2) . The surface of the contaminated item was sampled with a swab immersed in 10 mL of buffered peptone water (Swab-Samplers -3M, USA), and its content was used to analyze the number of viable particles on the surface for the control and after exposure to the disinfection chamber. For the control test, swabbing for microorganism collection was performed immediately after contamination; for the exposure tests to the biocidal agent, after 10 and 30 s. The control surfaces of each PPE analyzed were associated with both exposure experiments (10 and 30 s exposure). The antimicrobial action of sodium hypochlorite was neutralized by sodium thiosulphate [73, 74] . Sterile PPE items were used for each experiment, with a new item used for each microorganism or exposure time. In the second step, water-sensitive papers (WSP) (76x26 mm and 19.76 cm 2 area; Syngenta) were labeled from 1 to 6 and applied to the left side of the manikin (Fig 2) for exposure to the biocidal agent using the same exposure times and contamination sites of the first experiment. After each experiment, the papers were immediately stored in a desiccator with silica gel, and then images were recorded for qualitative analysis (observation of the paper color profile) of the deposition of biocidal agent on the surfaces of the PPE items. (6) shoe. For the control, the surface of the items was swabbed for microorganism collection immediately after surface contamination, while for the tests, the surfaces were swabbed after predetermined exposure times to the biocidal agent.

https://doi.org/10.1371/journal.pone.0250854.g002

Viable microorganisms in the swabbed samples were determined using a nutrient agar culture method specific for each type of microorganism, which were quantified from their growth in the plate [75] . The tests were performed immediately after the swabbed samples were collected. The samples were vigorously shaken to extract the microorganisms from the swab and release them into the saline solution so that they could be serially diluted (10 −1 to 10 −8 ). The dilutions were inoculated into the specific culture media and incubated according to the type of method. For E. coli, P. mirabilis and C. freundii, the VRBA count method was used; for P. aeruginosa, S. aureus, C. albicans and C. parapsilosis, the count of the total number of mesophilic microorganisms; and E. faecalis were counted by the EPA (US Environmental Protection Agency) method [70, 76, 77] . After quantification of the colonies under an optical microscope (Nikon Instruments), the results were expressed as log 10 CFU/mL and CFU/cm 2 . The number of CFUs was determined after incubation, and the number of CFUs per milliliter was calculated. The logarithmic scale (log 10 ) reduction factor was calculated using the formula RF = log 10 (A) -log 10 (B) (where A is the number of colonies recovered from the unexposed (control) surfaces and B is the number of colonies recovered from the exposed (test) surfaces) [56, 78] . The decimal percentage reduction in CFU/mL was calculated using the formula %R = [(A-B)/A] � 100 [79] .

Statistical analysis was performed using GraphPad Prism 8 (San Diego, CA, USA), where analysis of variance and Student's t-test were used to compare the means of the two groups (10 and 30 s), according to each test condition (microorganism x PPE item), with significance level of p <0.05. Principal component analysis (PCA) was performed using PAST version 3.26 (Oslo, Norway) with the means of the logarithmic reductions of each test condition to obtain the correlation between the analyzed variables (PPE-cap, safety glasses, respirator face mask, lab coat, glove, shoe and face shield-or surface type). Table 2 shows the results for the number of viable cells (CFU/mL and CFU/cm 2 ), the logarithmic reduction factor (log 10 ) of each assay compared to the respective control (without exposure to the biocidal agent), and the percentage reduction (%) after exposure to the biocidal agent in the disinfection chamber for 10 and 30 s for each test microorganism and for each individual PPE item evaluated in this study. Fig 3 shows the graphs of the logarithmic reduction (log 10 ) of each test microorganism per individual PPE item.

In total, 147 experimental conditions were studied, considering the two exposure times for each test microorganism (n = 98) and control (n = 49), as well as for the seven different types of PPE evaluated. In general, there was a significant reduction in the investigated microorganisms after exposure of the previously contaminated items in the disinfection chamber, regardless of the item, which demonstrated the efficacy of the biocidal agent spraying system for instantaneous disinfection of PPE for some of the microorganisms evaluated. In addition, the results showed that at 10 and 30 s, there was only a significant difference in the microbial load reduction factor during exposure of the biocidal agent to the microorganisms E. faecalis and P. aeruginosa (p >0.05). In this case, the exposure time of 30 s was more efficient for the inactivation of the studied microorganisms in terms of log 10 and percentage reduction for all studied PPE (Table 2 and Fig 3) .

A percentage reduction of >99% was determined for 96.93% (n = 95) of the tested conditions when compared to the control, while a percentage reduction of between 86.00-99% was Table 2 . Result of the number of viable cells in CFU/mL and their equivalent number in (CFU/cm 2 ), log 10 reduction factor (mean ± standard deviation) and percentage reduction for the microorganisms studied at 10 and 30 s of exposure to the biocidal agent in the disinfection chamber (results obtained from the comparative analysis with the control without exposure to the biocidal agent). found for 3.07% (n = 3) of the tested conditions. The lowest percentage reductions identified were 86.500 and 86.000% for the test with E. faecalis when the glove was evaluated at exposure times of 10 and 30 s, respectively. In general, the exposure time of 10 s to 0.25% sodium hypochlorite under the investigated conditions effectively reduced the microbial load by >99% for all investigated microorganisms, except for E. faecalis. For these microorganism, percentage reduction >99% at 10 s and 30 s of exposure was identified for all PPE, except for the glove and respirator face mask. It is noteworthy that the results related to the percentage reduction for the exposure time of 30 s were similar to the time of 10 s, except for E. faecalis ( Table 2 ). The percentage reduction is also reflected in the total number of viable cells, where 78.57% (n = 77) of the analyzed conditions corresponded to <10 CFU/mL or <0.33 CFU/cm 2 at 10 and 30 s of exposure to spraying of 0.25% sodium hypochlorite. In general, there was a reduction in the number of viable cells for all analyzed conditions when compared to the results found for the control group. The resistance to the biocidal agent under the investigated conditions of the microorganisms E. faecalis and P. aeruginosa was demonstrated in this parameter, since they were the only ones that showed viable cells in the concentration >10 CFU/mL or >0.33 CFU/cm 2 after the disinfection process in the chamber, with the exception of samples of P. aeruginosa collected from the face shield, glove and lab coat, at exposure times of 10 and 30 s, in addition to the shoe after 30 s of exposure. The exposure time of 10 s was able to reduce the number of viable cells for <10 CFU/mL or <0.33 CFU/cm 2 in 38 experimental conditions, while for the time of 30 s, this reduction occurred in 39 experimental conditions. The differences related to the recovery of microorganisms may be associated with resistance to the biocidal agent under the conditions tested, as well as the inoculum concentration. Fig 3 shows that E. coli was the microorganism with the highest log 10 reduction values, regardless of the analyzed experimental condition (PPE item/surface and exposure time), with values >9 log 10 . The microorganisms S. aureus, C. albicans, C. parapsilosis, C. freundii and P. mirabilis showed the same log 10 reduction at the tested exposure times, without significant difference regardless of the surface analyzed. It is important to highlight that for Candida species the log 10 reduction value was lower than the bacterial species and this effect may be due to the lower initial inoculum used. With regard to the PPE items, the lab coat showed the highest log 10 reduction values, varying between 4.30 log 10 (C. parapsilosis at 10 and 30 s) and 9.69 log 10 (E. coli at 10 and 30 s). The surface of the glove was the only one in which the log 10 reduction of E. faecalis was similar (p >0.05) at the exposure times of 10 and 30 s, with 0.87 and 0.85 log 10 , respectively, and was the lowest when compared to the reduction in the other analyzed surface. Fig 4 shows the results of the PCA applied to the different study variables, which in this study were related to the type of PPE (cap, safety glasses, respirator face mask, lab coat, glove, shoe and face shield). In PCA, the clustering of the samples defines the structure of the data through graphs of scores and loadings whose axes are principal components (PC) on which the data is projected. The scores provide the composition of the PCs in relation to the samples, while loadings provide that same composition in relation to the variables. The total variance of principal component 1, mainly influenced by the respirator face mask, was 78.31% and that of principal component 2, mainly influenced by the glove, was 16.01%, totaling 94.32% (Fig 4A) . The graph of the principal components shows that the microorganisms E. faecalis and P. aeruginosa were the only ones for which the samples from the 10 and 30 s exposure times did not (Fig 4B) . In addition, the graph shows the formation of clusters for all tested microorganisms at different exposure times. Clustering is important because it can indicate similar behavior among the samples evaluated according to the study variables. Note that the only analyzed fungi (C. albicans and C. parapsilosis) formed a cluster in the lower left quadrant, as well as the samples from 10 and 30 s of E. faecalis, having no influence on the type of surface/ item tested. However, the microorganisms S. aureus, E. coli, C. freundii and P. mirabilis clustered together in the lower right quadrant, being influenced by the type of surface/item tested (safety glasses, cap, respirator face mask and shoe), indicating that these microorganisms had similar behavior at the evaluated experimental conditions. P. aeruginosa was the only microorganism whose samples from 10 and 30 s were allocated in the upper right quadrant, not being influenced by the main analyzed variable, the PPE item. Note also that there was no negative correlation between the porous and nonporous surface variables for principal component 1, where all PPE correlated positively with each other (Fig  4c) . Thus, from the PCA analysis, it is observed that the type of microorganism analyzed influenced the results, since there was formation of clusters. In addition, even for the microorganisms that did not have overlapping values for the exposure times of 10 and 30 s, the behavior in response to the variables was similar since they remained in the same quadrant. observed ex situ after the WSPs were removed from the study surface areas (positions 1 to 6- Fig 2) . In general, there was good dispersion of the biocidal agent across the study area when using the disinfection chamber composed of the six nebulizer nozzles. The areas of the WSP with bluish tones show that there was deposition of the biocidal agent during the passage of the manikin through the disinfection chamber, while areas with yellowish tones indicate the absence of deposition of the studied agent.

In general, when comparing the distribution of the biocidal agent at the investigated exposure times, similar good deposition coverage of the agent on the WSPs was observed, which may be associated with the log 10 reduction profile of the studied microorganisms, where the exposure time to the biocidal agent had no significant influence on the reduction factor (except for E. faecalis and P. aeruginosa) ( Table 2 and Fig 3) . Thus, the amount of biocidal agent that reaches the study areas during the 10 s exposure would be sufficient to inactivate most of the investigated microorganisms. Qualitatively, greater deposition is observed in some points of the WSPs for the time of 30 s and this may explain the greater efficacy of the longer exposure time for the two most resistant microorganisms (E. faecalis and P. aeruginosa). In addition, the lower deposition of the biocidal agent on the respirator face mask (area 3), indicated by the yellowish tone, may have interfered with the reduction efficiency of these microorganisms. Fig 6 and S1 Table shows the results obtained for the stability analysis of the biocidal agent at a concentration of 0.25% by determining the pH (Fig 6A) and the percentage of active chlorine (Fig 6B) . The results showed that the sodium hypochlorite solution was stable over the evaluated period, with no significant difference (p >0.05) between the means determined for the pH and for the active chlorine concentration (%). These results demonstrate the viability of using the sodium hypochlorite solution with adequate active chlorine concentration (0.25%) for at least 20 days for application in the disinfection chamber, with maintenance of its disinfectant capacity.

In this study we demonstrated the high rates of microbial load reduction after exposure to the sodium hypochlorite biocidal agent used in the personal protective closes and equipment (PPE) disinfection chamber at the two analyzed times (10 and 30 s) regardless of the type of surface/PPE item investigated. Some studies [80, 81] and standards [79, 82] indicate that disinfection methods with �5 log 10 CFU reduction are considered effective and, consequently, appropriate for clinical use, which reinforces the importance of our results for the instant disinfection of PPE, especially during the SARS-CoV-2 pandemic. This logarithmic reduction implies the elimination of 99.999% of the microbial load [79, 82] . Considering these values as a reference, the microorganisms P. aeruginosa and E. faecalis showed the lowest sensitivity to sodium hypochlorite under the tested conditions (for some PPE items) when compared to the other microorganisms, although the results were quite satisfactory in relation to the reduction factor found for these bacteria under the studied conditions.

There are reports in the literature on the resistance of P. aeruginosa and E. faecalis to sodium hypochlorite at concentrations <0.3% and <0.22%, respectively [83, 84] . This mechanism may be associated with the bacterial ability to remove or discharge the charge of hypochlorous acid (HClO), which is a strong oxidizing agent that damages the permeability of the bacterial cell wall and its genetic material [85] . However, Lineback et al. [86] showed that the use of sodium hypochlorite at a concentration of 1.312% against P. aeruginosa was more effective than quaternary ammonium, while Yoo et al. [87] reported that this biocidal agent at 0.031% showed activity against clinical isolates of E. faecalis. In this study, the concentration of 0.25% of sodium hypochlorite was effective in reducing the load >99% for P. aeruginosa and �86.000% for E. faecalis.

Regarding the analyzed fungal strains, the percentage reduction value was >99% and the number of viable cell was <10 CFU/mL or <0.33 CFU/cm 2 for all experimental conditions, indicating that C. albicans and C. parapsilosis are sensitive to sodium hypochlorite under the tested conditions, which shows that spraying of the biocidal agent may be an effective alternative for the inactivation of these microorganisms when compared to other methods [62] . Infections caused by Candida species are classified as one of the main contaminants in the hospital environment because these pathogens can lead to systemic infection [88] . Although C. albicans is still the species most frequently isolated from nosocomial fungal infections [89] , cases associated with C. parapsilosis have increased significantly in recent years [90] due to the resistance of Candida species to antifungals and disinfectants [91] . Thus, it is important to note that spraying systems have been used to control bioburden in nosocomial environments, especially for combating multidrug-resistant strains [81] .

The study by Ishikawa et al. [37] demonstrated that the efficacy of a small disinfection chamber using a spray system with 5.00% sodium hypochlorite solution for the inactivation of Bacillus subtilis spores. The authors reported that the disinfection system used is a "test chamber", which does not have the physical structure for the passage of a person, being able only to perform the sporicidal effect in a small area [37] . However, unlike Ishikawa et al. [37] work, our study demonstrates the efficacy of a spray system (disinfection chamber) containing sodium hypochlorite for the instant disinfection of different PPE items (at 10 or 30 s) against Candida species and Gram-positive and Gram-negative bacteria on different types of surfaces at the same time. The efficacy demonstrated by the biocide agent in the concentration of 0.25% against the microorganisms tested suggests that new studies can be conducted using a lower concentration of the chemical agent, such as 0.1%, which is also in the concentration range recommended by WHO for the disinfection of environmental surfaces [49] .

Hospital infections are caused by factors such as environmental contamination, frequent handling of contaminated material, and the ability of microorganisms to survive for prolonged periods on different types of surfaces [1, 92] . Within the hospital environment, sodium hypochlorite is the most widely used disinfectant because it has broad-spectrum antimicrobial activity, considering Gram-positive and Gram-negative bacteria and fungi [83] as well as demonstrated virucidal activity [93] . Köhler et al. [94] showed that sodium hypochlorite effectively reduced the concentration of multidrug-resistant Gram-positive bacteria (Pseudomonas, Acinetobacter and Klebsiella) after exposure times of 1 to 15 min, longer exposure time than those studied in this work. Regarding the activity against viral agents, It has been demonstrated that sodium hypochlorite in concentrations between 0.01 and 0.5% is capable of inactivating the SARS-CoV-1 on stainless steel surfaces [95, 96] . In addition, Ma et al. [97] showed that instant hand hygiene using disinfecting wipes containing 0.05 or 0.25% active chlorine removed 96.62% and 99.98%, of the influenza virus, respectively, which causes avian influenza. The authors also point out that, although they have not tested with SARS-CoV-2, hand cleaning with the disinfecting wipes can help to control the spread of COVID-19. Similarly to the study by Ma et al. [97] , one limitation of our study was not to use SARS-CoV-2 as a test microorganism. However, based on the promising results identified in this study, which showed that the biocide capacity of sodium hypochlorite was maintained under the conditions tested, the evaluated concentration of 0.25% has the potential for disinfecting surfaces contaminated by different microorganisms and can be extrapolated to enveloped viruses based on results in the literature, being a potential agent against SARS-CoV-2. The choice of evaluating different bacteria and fungi as biological indicators stemmed from the need to accelerate the confirmation of the disinfectant action of the proposed technology, since some of these microorganisms are resilient compared to viruses [98] , have a relatively faster growth and can be manipulated in laboratory environments with a lower level of biosafety.

Other studies have already demonstrated the effect of different biocidal agents against the microorganisms tested in this study, showing that the efficacy of the disinfection process varies with the type of disinfectant [99, 100] or according to the application method used [101, 102] . There are few reports in the scientific literature on the efficacy of PPE decontamination after exposure to pathogens, as was analyzed in this study. Among them, Lemmer et al. [103] showed that disinfection with 2% peracetic acid with 0.2% surfactant through a spray system was able to inactivate B. thuringiensis spores in high density polyethylene protective coveralls after 5 min of exposure. Compared to our study, sodium hypochlorite was more effective than peracetic acid because the exposure time required was shorter to reduce the microbial load on the surface, considering the polyethylene surface and other analyzed materials. In addition, the instantaneous decontamination demonstrated by the results obtained in 10 and 30 s exposure times shows the potential of the disinfection chamber application in places with intense or moderate people flow, such as the exits of intensive care units and wards in hospitals. In addition, reducing the microbial load on the surface of PPE can help reduce the risks associated with handling and exposure to biomedical waste, an important source of environmental contamination [104] .

The results also suggest that the use of sodium hypochlorite may be recommended due to the stability of its solution in terms of pH and concentration of active chlorine over the 20 days, since the exchange or replacement of the biocide agent solution does not need to be performed, for example, on a daily basis. The dissociation of NaOCl into HOCl-, its main active agent, is pH-dependent [105] . Thus, it is important that the solution remains stable so that the levels of the active agent do not decrease. The critical issue raised by health authorities' agencies are sodium hypochlorite toxicity when in contact with mucous membranes and may lead to tissue damage or allergic reactions [106, 107] . Therefore, we are aware of the possibility of episodes of clinical toxicity caused by the sodium hypochlorite, especially in persons that are known to be allergic to bleaches, and that this can be considered as a limitation of the study. In addition, we re-emphasized that the disinfection chamber with 0.25% sodium hypochlorite be used only by fully trained workers (considering its installation, the preparation of the biocide agent in the correct concentration, and for its correct use), thus promoting an effective disinfection process against bacteria and potential emerging pathogens, such as SARS-CoV-2, that is safe for users.

The use of the proposed disinfection technology becomes an attractive alternative, especially for middle-income countries such as Brazil [38] . This occurs due to factors such as the material used in the chamber framework, which are widely used in the industry for the manufacture of different items, its modular design that allows scalable production as well as the lowcost of sodium hypochlorite. These factors can make production cheaper and facilitate transport and installation in different health facilities. In addition, the results obtained related to WPS showed that the nebulizer nozzles disposition promoted a satisfactory spraying of the biocide agent.

Indeed, disinfection chamber could be considered as an interesting disinfection technology for use in emerging countries, since it can improve the control cases of nosocomial infection in those places that usually have the most overloaded health systems.

The disinfection chamber proved to be a potential technology for the rapid and effective disinfection of the surface of PPE, regardless of the evaluated item, routinely used by HCWs for protection against infectious agents. The spraying system with the biocidal agent was effective in reduce the microbial load, where the percentage reduction equal to >99% and, consequently, bringing the number of viable cells to <10 CFU/mL and <0.33 CFU/cm 2 after exposure times of 10 and 30 s in 96.93% of the experimental conditions analyzed. The lowest percentages reduction were found for the sample of E. faecalis collected from the glove, where the values obtained were 86.000 and 86.500% for the exposition of 10 and 30 s, respectively, while the highest amount of viable cells was found for P. aeruginosa sample at 10 s in the cap, with 7.7x10 5 CFU/mL or 2.6x10 4 CFU/cm 2 . The log 10 reduction values varied between 0.85 log 10 (E. faecalis at 30 s in glove surface) and 9.69 log 10 (E. coli at 10 and 30 s in lab coat surface).

Thus, the bacterial species E. coli, S. aureus, C. freundii and P. mirabilis and the fungi C. albicans and C. parapsilosis showed susceptibility to 0.25% sodium hypochlorite under the evaluated experimental conditions independent of the exposure time or PPE item evaluated, while the microorganism E. faecalis was less susceptible to the biocidal agent under the tested conditions. In general, a 30-s exposure time was more efficient in reducing the investigated microbial load.

The results of this study show that the disinfection chamber with 0.25% sodium hypochlorite may be an alternative to control the bioburden in nosocomial environments, especially to prevent the self-contamination of HCWs in the doffing step. The importance of the use of the chamber by properly attired HCWs is also emphasized in order to avoid direct contact with the tested biocidal agent. In addition, because this is a novel study, these results may contribute to the development and safe use of disinfection equipment in environments where the environmental bioburden must be controlled. It is also important to highlight that the experimental design of the study was carried out in order to have a simulation of how the disinfection chamber would be used by HCW in the nosocomial environment. Thus, the manipulation of viral strains would not be appropriate in the conditions tested, since the handling of these microorganisms requires a laboratory environment with a higher level of biosafety. However, although virucidal efficacy was not directly determined, the chamber may be an alternative to reduce the contamination rates among HCWs in front of different types of emerging microorganisms, reducing the impacts in the area of public health. 

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The authors thank Bahia Department of Health (Secretaria de Saúde do Estado da Bahia-SESAB), Directorate of Sanitary and Environmental Surveillance of Bahia (Diretoria de Vigilância Sanitária e Ambiental do Estado da Bahia-DIVISA BA) and Hospital Espanhol of Salvador (COVID-19 Campaign Hospital).