Effectiveness of a low-cost UVGI chamber for decontaminating filtering facepiece respirators to extend reuse

Abstract In emergencies like the COVID-19 pandemic, the reuse or reprocessing of filtering facepiece respirators (FFRs) may be required to mitigate exposure risk. Research gap: Only a few studies evaluated decontamination effectiveness against SARS-CoV-2 that are practical for low-resource settings. This study aimed to determine the effectiveness of a relatively inexpensive ultraviolet germicidal irradiation chamber to decontaminate FFRs contaminated with SARS-CoV-2. A custom-designed UVGI chamber was constructed to determine the ability to decontaminate seven FFR models including N95s, KN95, and FFP2s inoculated with SARS-CoV-2. Vflex was excluded due to design folds/pleats and UVGI shadowing inside the chamber. Structural and functional integrity tolerated by each FFR model on repeated decontamination cycles was assessed. Twenty-seven participants were fit-tested over 30 cycles for each model and passed if the fit factor was ≥100. Of the FFR models included for testing, only the KN95 model failed filtration. The 3M™ 3M 1860 and Halyard™ duckbill 46727 (formerly Kimberly Clark) models performed better on fit testing than other models for both pre-and-post decontaminations. Fewer participants (0.3 and 0.7%, respectively) passed fit testing for Makrite 9500 N95 and Greenline 5200 FFP2 and only two for the KN95 model post decontamination. Fit testing appeared to be more affected by donning & doffing, as some passed with adjustment and repeat fit testing. A ≥ 3 log reduction of SARS-CoV-2 was achieved for worn-in FFRs namely Greenline 5200 FFP2. Conclusion: The study showed that not all FFRs tested could withstand 30 cycles of UVGI decontamination without diminishing filtration efficiency or facial fit. In addition, SARS-CoV-2 log reduction varied across the FFRs, implying that the decontamination efficacy largely depends on the decontamination protocol and selection of FFRs. We demonstrated the effectiveness of a low-cost and scalable decontamination method for SARS-CoV-2 and the effect on fit testing using people instead of manikins. It is recognized that extensive experimental evidence for the reuse of decontaminated FFRs is lacking, and thus this study would be relevant and of interest in crisis-capacity settings, particularly in low-resource facilities.


Introduction
The COVID-19 pandemic posed a severe threat to public health, occupational health, and local economies worldwide (Cassorla 2021), overwhelming healthcare systems and the stock of filtering facepiece respirators (FFRs) (Rowan and Laffey 2020). Despite being the last alternative in the hierarchy of controls, wearing appropriate and well-fitted FFRs is still one of the most effective preventative measures, particularly in poorly controlled areas and in settings where exposure is unknown or unpredictable (Sehgal and Milton 2021). However, the shortage of FFRs and the use thereof for periods beyond that recommended may contribute to anxiety and the high incidence of COVID-19 infections among health workers and other end users (De Kock et al. 2021;Ruskin et al. 2021).
With the possibility of future COVID-19 waves, among other airborne biological threats, the need for an adequate stock of quality FFRs to reduce the risk of exposure is of paramount importance and life-saving (Rashid et al. 2022). The Centers for Disease Control and Prevention (CDC) recognized the need to optimize the supply of N95 respirators and recommended contingency capacity strategies which include the reuse and extended use of N95 respirators . Accordingly, healthcare workers could rotate FFRs over five days between each FFR use, providing time for pathogens to "die off" during storage (3M Science 2020). However, aside from pathogens with prolonged inanimate surface survival, the SARS-CoV-2 virus can survive on a mask for up to seven days (Cordoba-Lanus et al. 2021), implying that extended use in the absence of decontamination may pose an infectious risk to wearers (Schwartz et al. 2020;). Thus, the need for effective solutions prompted an international plethora of innovations in decontaminating FFRs for reuse in resource-limited contexts (Byrne et al. 2020;Rothe et al. 2020;Cassorla 2021;Cordoba-Lanus et al. 2021).
While SARS-CoV-2 has a global impact, people living in low-and middle-income countries (LMIC) were particularly impacted by COVID-19 (Bong et al. 2020). The impact transcended certain disposable respirators' availability, leaving many nations that lacked manufacturing capacity in dire straits (Vanhooydonck et al. 2021). Local manufacturing was hampered by staggering costs and a lack of access to core materials used in product processing. Based on the unprecedented crisis and FFR shortages, decontamination and reuse as a crisis capacity strategy ensure continued availability for frontline workers in lowresource settings.

Decontamination or reprocessing of FFRs
Decontamination or reprocessing of single-use FFRs was accepted in 2020 as a crisis strategy to conserve available supplies (CDC 2020). Limited decontamination and reuse of FFR are advised for NIOSHapproved respirators only (CDC 2020). The CDC's recommendations to conserve FFR supplies include extended use (longer wearing time and/or use with multiple patients), prioritizing use for those at the highest risk, and limited reuse (CDC 2020). This manuscript includes some preprint reports that have not yet benefited from a peer-review process.
Ultraviolet germicidal irradiation (UVGI) was selected as a decontamination method in the current study as it has been reported as one of the better decontamination methods available (Schumm et al. 2021;van der Vossen et al. 2022). Schumm et al. (2021) conducted a systematic review of FFR reprocessing and reported 27 studies that evaluated UVGI. Several N95 respirators (n ¼ 43) were treated with UVGI at doses between 1 and 2 J/cm 2 and effectively decontaminated most pathogens (>3 log reduction), including influenza virus, MS2 bacteriophage, Bacillus spores, vesicular stomatitis virus, Middle East Respiratory Syndrome (MERS) virus, and SARS-CoV-2 without degrading respirator components.
The included studies had several limitations. Many were experimental laboratory-based studies except for two studies that examined clinical use. Only five studies directly evaluated SARS-CoV-2, whereas other studies inferred from other viral and bacterial surrogates Rothe et al. (2020) highlighted that although a large volume of data on mask disinfection and reuse existed, much was not comparable as many studies lacked specificity on methods and tested a wide range of conditions on a small number of samples.
Considering there are over 530 NIOSH-certified FFRs, the results from previous studies cannot be generalized to all FFRs models, rather, specific FFR testing should be considered the FFR model (e.g., shape, material), decontamination method, and filtration performance, facial fit, and residual toxins (Wharton and Rieker 2020). In addition, independent confirmation of reused FFR safety and fit is warranted as most studies used manikins rather than FFR worn by humans (Allen et al. 2020;Arnett 2020). Of the few studies that assessed user fit, one reported good quantitative fit and filter function of one FFR after ten cycles of 216 mJ/cm 2 to each side, an atypically low dose (Ou et al. 2020). Contrary, another study reported that all six samples of three models failed filter and human fit tests after 10 UVGI cycles without a reportedosesse (Rutala et al. 2019).
The UV-C intensity is critical to the method's success at disinfection, as an insufficient dose will not inactivate infectious material (Boskoski et al. 2020;Liao et al. 2020). While the dose used in previous studies varied from 2 to 5 J/cm 2 (Mills et al. 2018;Fischer et al. 2020), the recommended dose (1 J/cm 2 ) reported by Heimbuch and Harnish (2019) was 100 times higher than that required for hard surfaces (Grossman et al. 2020). Unlike solid surfaces, respirator material requires higher UVGI doses for decontamination because it needs to penetrate the material layer/s. The spatial distribution of UV-C intensity is not uniform and varies significantly with distance from the light source, which must be in the direct path of a pathogen to inactivate it; hence, multiple light sources or separate cycles for each side may be required (Heimbuch et al. 2011;Mills et al. 2018;Heimbuch and Harnish 2019;Jacobs et al. 2020).
Concerns regarding varied FFR styles, the potential for attenuation, shadowing, and strap damage have been raised (Tseng and Li 2007). FFR model differences as well as varying treatment doses cause significant variations in UVGI efficacy (Lindsley et al. 2015;Mills et al. 2018;Heimbuch and Harnish 2019;Fischer et al. 2020;Liao et al. 2020;Syphers 2020;Weaver et al. 2020). Therefore, it would be useful to categorize model types based on shape or determine how findings for a specific model can be generalized so that each model does not need to be evaluated (Derraik et al. 2020). It is thus essential to determine how many UVGI decontamination cycles an FFR model can sustain without compromising structural and functional integrity and effectively inactivating the target organism/s within the local context and based on the available resources. Considering the above, this study aimed to investigate a low-cost UVGI chamber for decontaminating FFRs contaminated with SARS-CoV-2. The study also evaluated the performance criteria (facial fit and filtration efficiency), structural integrity, odor, and user safety.

Methods
This experimental design evaluated the impact of 30 repeat decontamination cycles on seven FFR models and the functional performance using a low-cost UVGI chamber. Duplicate FFRs were tested before and after each decontamination cycle to a maximum of 30 cycles. One batch was used for fit testing and the second was for filtration testing. Twenty-seven consenting participants were included in the study, 7 were male and 20 females, of which 18 were Black Africans, 5 Asians/Indians, and 4 were White hence accounting for various facial dimensions. A batch of new FFRs without viral contamination was worn by the participants for the duration of fit testing and repeatedly until the 30 th fit test cycle unless fit testing failed before the 30 th cycle, and were coined "used" or "worn-in." Post decontamination, the FFRs were visually and tactilely assessed for structural integrity and underwent quantitative facial fit testing to assess functional integrity.
Performance tests also included filtration efficiency testing and SARS-CoV-2 inactivation by UVGI. Ethical clearance for the study was acquired from the REDACTED.

Filtering facepiece respirator selection
Seven FFR models available to frontline and essential workers in South Africa at the beginning of the pandemic were included in this study, of which four models were N95s, two were FFP2s, and one was a KN95 (Table 1). The FFRs consisted of electrostatically charged polypropylene filters (electret filter media). All FFRs were verified from the same respective manufacturing batches/lots at the beginning of the study to reduce any batch-to-batch variation during testing.

Decontamination method
A custom UVGI chamber was developed specifically for FFR decontamination applications to be low cost, simple to operate, safe, and use readily available components. The primary design principle is based on a drawer/rail mechanism that is either in an "OPEN" or "CLOSED" position, as shown schematically and physically in Figure 1a. To reduce the potential idle time of the process, FFRs are positioned onto a removable carrier frame to enable the FFR positioning procedure to occur simultaneously during a batch decontamination cycle. Predetermined positions were established for each FFR model, where the straps of the FFRs were carefully positioned onto locating rods of the carrier frame to open the respirators, avoiding shadows and contact with other respirators from hanging straps while preserving the structural integrity ( Figure 1b). The chamber could accommodate different FFR model types classified as a "cup shape" (3M-1860-N95; 3M 8810SSA-FFP2; Makrite 9500-N95) or "fold shape" (duckbill 46727-N95 with a horizontal fold, or the KN95 CE 2703-N95 and Greenline 5200-FFP2 with vertical folds). However, FFRs made with pleated material such as the 3M V-flex 9105S-N95 were not considered suitable due to anticipated selfshadowing effects and were excluded from subsequent testing.
In the "OPEN" position, the carrier frame was loaded and unloaded onto a vertical drawer that slides into the chamber. Transient startup characteristics of UV-C lamps require a warm-up time for the output to stabilize. The configuration of the drawer/rail geometry eliminates the need to turn the lamps on or off between cycles, which is ideally suited to batch processing. The chamber, therefore, incorporated a long drawer-travel length with panel arrangements to protect operators (Figure 1c). Further details about the UVGI chamber design and process testing can be found in the supplementary material online.

Quality indicators for FFR reprocessing
Reprocessing of FFRs (decontamination and reuse) was measured using three quality indicators, including physical integrity/performance of the respirator (filtration efficiency and facial fit), safety for users, and effectiveness of pathogen reduction. In addition, each respirator was qualitatively evaluated for any soiling, damage, degradation of the FFR, or other defects. The FFRs were visually inspected pre-and-post decontamination and before fit testing to ensure all indelible markings are legible, based on an agreement between two people evaluating legibility (FDA 2020a).

Filtration efficiency
A total of 186 filtration efficiency tests were conducted including each FFR model after each decontamination and a control sample for each FFR model that was not subjected to decontamination. The test parameters and requirements for the inert aerosol collection efficiency testing were based on the SANS 50149 which is equivalent to EN 149. The filter material's penetration was assessed by passing sodium chloride through the respirator at 95 L/min, using the TSI Certi Tester 8130 instrument (Protechnik Laboratories, a division of Armscor SOC LTD, South Africa). The instrument controls the generation of sodium chloride particle generation with the flame photometer as the detector. The test acceptance criteria were !94% filtration efficiency using a particle size distribution between 0.02 mm 2.03 mm equivalent aerodynamic diameter with a mass median diameter of 0.6 mm (or directional cumulative leakage of 6%).

Facial fit testing
Fit testing was performed on 27 participants following clearance for COVID-related symptoms. Subjects with beards or stubble, smoking within 30 min of fit testing, and those who were asthmatic or had respiratory conditions were excluded. All participants were briefed on the procedure's principle, the correct donning and doffing, and conducting a seal check before they were fit tested. The respirator donning included adjustments until a satisfactory fit was felt; however, no adjustments were allowed during the fit testing. A calibrated TSI PortaCount Pro þ Model 8038 (Bopp et al. 2020) using the OSHA-Modified (CNC) Fit Test Protocol with four exercises (bending over, talking, moving head from side-to-side and moving head up and down) (OSHA 2018) was used. These exercises aimed to stress the respirator seal in ways that simulate anticipated workplace motions. The PortaCount tester uses condensation nuclei counting (CNC) technology to count individual particles inside and outside the respirator to determine a quantitative estimate of the respirator fit factor. A batch of respirators was decontaminated with every cycle before each round of testing. For acceptance, the fit factor had to be !100, whilst a factor <100 was captured as the last test.
Retesting was also discontinued if an FFR was damaged or soiled, or the user did not obtain a seal.
A clinical isolate of SARS-CoV-2 ($1.4 Â 10 5 plaques forming units (PFU)/mL) at passage three was propagated in Vero E6 cells to generate a working stock. A confluent flask (!90%) was infected with 1 mL SARS-CoV-2 and allowed to absorb for 1.5 hr in an incubator (ThermoForma, US) at 37 C with 5% CO 2 , shaking every 15 min. After three days, when widespread cytopathic effect (CPE) was observed, the supernatant was collected, spun for 5 min at 3000 g on a benchtop centrifuge (Hettich, Germany), aliquoted in 2 mL tubes, and stored at À70 C until analysis (Thermo Electron Corporation) (Campos et al. 2020).
For tissue culture infection and cell culture viability, the stock virus suspension aliquots were thawed using a water bath (37 C) for 2 min (FMH Instruments) before use and inoculated into 24 hr old Vero E6 monolayer cells. The cultures were then incubated for approximately 72 hr in a 5% CO 2 incubator and observed for cytopathic effects using an inverted microscope (Leica DMIL). Cell viability was determined using the Countess cell counter (Olympus, Japan).
Swatches excised (1 cm in diameter) from previously worn FFRs (i.e., FFRs used for fit testing) were decontaminated before impregnating the viral aliquots (150 lL) onto the outer surface to simulate the "real" contamination and were subjected to 1-hr adsorption at 25 C. The swatches and metal disks were divided into two groups, A (not decontaminated) and B (decontaminated). Group B FFRs were exposed to UV within the chamber as indicated in Figure 1 and thereafter were subjected to extraction in 5 mL of viral transport media (VTM), vortexing, and centrifuging at 12,000 g for 20 min. A viral transport medium (5 mL) was used to extract SARS-CoV-2 from the contaminated FFR sample swatches (FFRs of Group A and B) and the metal disks.
The microbial log reductions were determined using a modification of the ASTM E-2197 quantitative swatch carrier method since there was no standardized method to evaluate the antimicrobial effectiveness of UVGI technologies. This was achieved by comparing the concentration recovered from the test swatches pre-and-post decontamination process (Havill et al. 2012). A set of non-spiked FFRs and metal disks were also tested to establish the baseline performance. For this study, decontamination was considered with a reduction of !3 log in pathogen load after reprocessing, corresponding to greater than 99.9% inactivation of least resistant pathogens (lipid or medium-sized viruses) (FDA 2020a(FDA , 2020b(FDA , 2020c.

Statistical analysis
All measurements were logged on datasheets and exported to STATA 16 (Stata Corp College Station, Texas, USA) for statistical analysis. Numerical variables were reported as mean and standard deviations or medians and interquartile ranges, while categorical variables were expressed as percentages. Changes in FFR fit were analyzed by comparing to the cutoff (!100) and decontamination categories in intervals of five. The filtration penetration changes were determined by comparing the results of each decontamination cycle to the filtration efficacy cutoff (<6%). The log (formula 1) and percentage reduction (formula 2) were used to assess the reduction in the virus's concentration after decontamination.
Log reductionðRÞ ¼ log 10 C A À log 10 C B where C A and C B are concentrations of the virus, before and after decontamination.

FFR physical observation
Four participants reported FFR 3M8810SSA strap failures across the 30 cycles performed, where the elastic bands were difficult to stretch post-decontamination and were prone to snapping (Table 2). Forty-eight reports (13%) regarding a burning smell after UVGI decontamination for all FFR models but mostly for 3M1860 (4.9%), 3M8810SSA (4.2%), and Duckbill (2.6%) were noted. No degradation was observed for any of the control FFRs that were not subjected to any decontamination.

SARS-CoV-2 inactivation
Post-decontamination there was a reduction in infected cells for all FFR samples with the highest reduction observed for Greenline 5200 (99.998%) and Duckbill (98.723%) (Figure 2). The Greenline 5200 FFR achieved an average 4 log reduction. None of the other FFRs achieved !3 log reduction with repeat experiments (Table 5), which is important to demonstrate repeatability and reproducibility. However, single experiments demonstrated up to 5 log reductions for Duckbill, Makrite 9500, 3M8810SSA, Greenline 5200, and Wenzhou, but not 3M1860 (data not shown).

Effect of UVGI decontamination on FFRs
The current study used a maximum of 1.2 J/cm 2 with varying exposure times to achieve the intended dose for different FFR design configurations. With the targeted dosage, 1.1% strap failure was noted and 13% burn-like odor reports post UVGI decontamination. Our findings are similar to previous reports regarding the fragmentation of the elastic material in the straps when stretched (Schumm et al. 2021). Another study also reported an "intolerable odour" of one FFR treated with UVGI (Goyal et al. 2014). Although the odor phenomenon appears to be common for UVGI technology and nothing suspicious; an odor is not ideal. The odors appear to dissipate after approximately 4 hr, hence should be considered when using UVGI (Heimbuch and Harnish 2019).

Effect of repeated UVGI decontamination on filtration
The UVGI decontamination method preserved filtration efficiency for all FFRs tested except the Wenzhou KN95 respirator. Nevertheless, we found that 53 fit tests using the Wenzhou KN95 with repeated UVGI decontamination passed, although, the filtration efficiency test failed on all cycles; highlighting the importance of a comprehensive validation before implementation of any FFR decontamination protocol.

Effect of repeated UVGI decontamination on facial fit
Our study showed that depending on the FFR type, some could withstand 30 cycles of donning and doffing. We showed that wear and tear from donning and doffing with repeated use might damage the respirator faster than repeated decontamination. We demonstrate Makrite failure after five cycles of fit testing, possibly due to its firmer shape resulting in a poor facial fit and increased leakage. Therefore, donning and doffing practices, storage conditions, and the duration of use may be critical determinants of fit test failures (Bioquell 2016;Vuma et al. 2019;Smullin and Tarlow 2021). For this reason, FFRs should be assigned to one wearer even when reused as nose clips Key: Filtration cutoff: <6%, meanarithmetic mean, SDstandard deviation, 3M 1860 was not tested due to stock shortages. Controlrespirators that were not exposed to any decontamination process.   and headbands adjust to the wearer's face and impact fit and seal (O'Kelly et al. 2021).
The researchers also demonstrated that fit testing alone might be insufficient in assessing FFR effectiveness as a few individuals passed despite the respirator failing the filtration efficiency test for Wenzhou KN95, even before decontamination. The results also show that it cannot be assumed that one respirator will fit a work cohort and that whichever FFRs are used are validated against the decontamination method. The number of decontamination cycles is limited by mechanical wear and/or soiling of FFRs, rather than cumulative UV-C exposure. The physical appearance, odor, and laboratory performance (filter aerosol penetration and filter airflow resistance) of six N95 FFRs models after three cycles of decontamination with UVGI were also not affected (Bergman et al. 2010). Our results corroborate other findings (Fischer et al. 2020) regarding the number of cycles while maintaining the fit testing integrity after more than one cycle.
The investigators had no operator symptom reports, and thus the prototype is safe for operators in the short term. The World Health Organization considers, among others, the use of UV-C in reprocessing PPE under severe shortage (Frigerio 2020). The UVGI cabinet designed for this study provides an easily constructed, cost-effective solution using locally available components, with sufficiently high and scalable throughput to meet the demands of small hospitals, clinics, and first responders who experience FFR shortages. The authors acknowledge that in some reduced or low-resourced settings, UVGI may not be feasible owing to infrastructure (electrical) or other resources.

Inactivation of UVGI decontamination on SARS-CoV-2 contaminated FFRs
The percentage reduction of SARS-CoV-2 impregnated on the six FFR models differed, with one (Greenline 5200 FFR) achieving a ! 3 log reduction (99.9%) using UVGI. These findings concur with the literature , showing that a UV-C irradiation dose ! 1 J/cm 2 at the FFR surface inactivates SARS-CoV-2 (Ozog et al. 2020) and its predecessor SARS-CoV (Heimbuch and Harnish 2019) by ! 3 log reduction on most tested N95 facepieces, while our study only achieved a ! 3 log reduction with SARS-CoV-2 on one FFR. Bergman et al. (2010) also demonstrated the UVGI decontamination effectiveness of six N95 FFRs models after three cycles; however, their study's limitation was that only the exteriors of the FFRs were exposed. UVGI rapidly inactivates SARS-CoV-2 on steel but more slowly on N95 fabric, likely due to its porous nature (Bergman et al. 2010), and is protected from inactivation if it penetrates deep into the layers of the FFR as UVGI may not penetrate the deeper layers (Lindsley et al. 2015). However, another study that "sandwiched" the spores strips between two N95 FFRs layers showed a 6-log inactivation in all locations after a single dose of 1 J/cm 2 (Purschke et al. 2020). This is an important finding supporting our results that UVGI is suitable the for decontamination and reuse of FFRs. In addition, a report commissioned by the FDA (2019) reported that N95 samples with hydrophilic surfaces showed consistent mean viral reductions lower than 10 3 while those with hydrophobic surfaces showed mean viral reductions greater than 10 3 (Heimbuch and Harnish 2019). Another study reported similar findings (Ozog et al. 2020). UVGI decontamination demonstrated significant reductions in influenza virus recovery and viability from N95 even with soiling conditions (mucin and sebum-soiled facepieces). It has shown a significant reduction in the recovery of B. subtilis, inactivation of 99.9% to 99.999% of respiratory viruses such as Influenza A (H1N1), Avian Influenza A virus (H5N1), Influenza A (H7N9) A/Anhui/1/2013, Influenza A (H7N9) A/Shanghai/1/ 2013, MERS-CoV, and SARS-CoV and inactivation of SARS-CoV-2. The inactivation of the target microorganism/s is a critical factor in considering the effectiveness of any decontamination method. The FDA recommends a 6 log reduction corresponding to the highest level of resistance (bacterial spores) when a decontamination system is intended for multiple users due to the increased risk of transmission of individuals' bioburden or a ! 3 log reduction of non-enveloped viruses/Gram-positive/Gram-negative bacteria for single-use to supplement existing CDC reuse recommendations (FDA 2020c).
Three studies showed virucidal inactivity of > 3 log reduction of SARS-CoV-2 using UVGI (Fischer et al. 2020;Ozog et al. 2020;Smith et al. 2021), however, each had a small FFR sample, mainly of the 3M models and no filtration efficiency testing was done in two of the studies, while two did fit testing on few cycles. Smullin and Tarlow (2021) reported that SARS-COV-2 inactivation occurs spontaneously at room temperature; however, the timing depends on humidity, temperature, and surface material. Therefore, extended use without decontamination may increase the risk of exposure to microorganisms with long survival times. Owing to variability in room temperature conditions and FFRs, assigning a precise 3log decay time for all used N95 FFRs is impossible (Smullin and Tarlow 2021). Moreover, the time to get from 1000 active particles to 1 active particle is the same as getting from 5,000 to 5 active particles. The fact that we did not achieve as high log reduction for all FFRs as others (Rothe et al. 2020) could imply that the doses used were insufficient to damage the vital macromolecules for replicating pathogens impregnated on different FFR materials and surfaces. Thus, further investigations into higher doses, which are still safe for the end-user, are warranted for the other FFRs.
According to public reporting, extended use and re-use of FFRs have become common in hospitals in areas where SARS-CoV-2 is high. However, the appropriate decontamination and subsequent re-use of FFRs should not pose a health risk to the already taxed healthcare workers (Kumar et al. 2020). Our study shows that certain FFR's use can potentially be extended several-fold without degradation of functional integrity depending on the type of material used and natural variability due to the target agent's "biological" nature. Care was taken to ensure controlled irradiance distribution over the FFR surface; however, the Vflex respirator was unsuitable for UVGI decontamination due to the pleated material.
While the actual efficacy of the UVGI system used may not have been fully optimized given the time constraints; extensive efforts were made to ensure the parameters are in line with what is used with success globally. The prototype design considered several challenges associated with UVGI for FFR applications, including shadowing and repeatable mask mounting. The final configuration resulted in a unit that can accommodate four FFRs per cycle, a system that is easy and safe to operate. It is noted that, in general, processes are effective within a specific operating environment/envelope only. The prototype can be enhanced to increase production throughput, and reduce the device's size and cost.
Although the effectiveness of decontamination with UVGI is not in dispute, and the evidence indicates that the integrity of the respirators is not significantly affected using the decontamination process, some serious concerns are raised regarding quality assurance and user safety. Hence, based on our findings, it is suggested that decontamination be used only for single users and a protocol be established to manage the logistics and quality thereof. The loss of health workers to preventable illnesses due to inadequate access to quality RPE is unacceptable. Therefore, it is envisaged that the current findings add to the growing body of evidence regarding the efficacy of decontamination of FFRs for low-resource settings, among other settings.
The investigators recognize that placing liquid aliquots of SARS-CoV-2 on the outside of the FFR filter compared to the collection of infectious particles within a filter by inhalation is a limitation. However, using SARS-CoV-2 in these experiments is complex and sensitive to several factors (e.g., type of cell line, age of cell line, the pathogenicity of strain, the timing of infectivity, environmental conditions, etc.). Nonetheless, efforts were made to ensure the parameters are similar to what is used with success globally.

Conclusion
This study comprehensively evaluated the efficacy of a low-cost UVGI chamber as a promising method for decontaminating FFRs and verifying the bioburden reduction of SARS-CoV-2. A ! 3 log reduction of SARS-CoV-2 was achieved with worn-in Greenline 5200 FFRs using UVGI. The respirator's ability for reuse was demonstrated even after multiple cycles (up to 30) of decontamination as the fit factor and filtration efficiency did not significantly deteriorate for 27 users and the FFRs types tested. The low-cost UVGI cabinet design can be used in facilities with low throughput. However, decontamination and re-use of FFRs are model-specific, thus, facilities must validate the methods for the type of FFR used.

Recommendations
The number of times an FFR can be reused is restricted by its failure in maintaining a good fit with repeated use rather than by the degradation from the decontamination process itself. Hence, manufacturers should consider using more durable straps. There is, unfortunately, no single FFR decontamination and reuse solution for all FFRs and settings. Each individual or facility must select and tailor a solution according to their needs, capability, and available resources. Given the current high demand, usage, and cost of FFRs, the fact that decontaminated FFRs still offer significant user protection, and the comparatively low cost of decontamination, the benefit of increasing FFR reserves should easily outweigh the application costs. If a third of the FFRs could be decontaminated and put back into the system, considerable costs could be saved as well as ensure the safety of frontline and essential workers, which is paramount. It must be reiterated that FFR decontamination should be implemented as a risk-mitigation strategy during crisis capacity conditions only and with proper engineering, industrial hygiene, and biosafety controls.