Ilaria Armentano1, Marco Barbanera1, Elisa Belloni2, Silvia Crognale3, Davide Lelli3, Marco Marconi1, Giuseppe Calabrò1. 1. Department of Economics, Engineering, Society and Business Organization (DEIM), University of Tuscia, Viterbo 01100, Italy. 2. Department of Engineering, University of Perugia, Perugia 06125, Italy. 3. Department for Innovation in Biological, Agro-Food and Forest Systems (DIBAF), University of Tuscia, Viterbo 01100, Italy.
Abstract
This paper deals with the design of a compact sanitization device and the definition of a specific protocol for UV-C disinfection of a surgical face mask. The system was designed considering the material properties, face mask shape, and UV-C light distribution. DIALux software was used to evaluate the irradiance distribution provided by the lamps emitting in the UV-C range. The irradiance needed for UV-C-decontaminated bacteria and virus, and other contaminating pathogens, without compromising their integrity and guaranteeing inactivation of the bacteria, was evaluated. The face mask's material properties were analyzed with respect to UV-C exposure in terms of physicochemical properties, breathability, and bacterial filtration performance. Information on the effect of time-dependent passive decontamination at room temperature storage was provided. Single and multiple cycles of UV-C sanitization did not adversely affect respirator breathability and bacterial filtration efficiency. This multidisciplinal approach may provide important information on how it is possible to correctly sanitize a face mask and, in case of shortage, safely reuse the face mask.
This paper deals with the design of a compact sanitization device and the definition of a specific protocol for UV-C disinfection of a surgical face mask. The system was designed considering the material properties, face mask shape, and UV-C light distribution. DIALux software was used to evaluate the irradiance distribution provided by the lamps emitting in the UV-C range. The irradiance needed for UV-C-decontaminated bacteria and virus, and other contaminating pathogens, without compromising their integrity and guaranteeing inactivation of the bacteria, was evaluated. The face mask's material properties were analyzed with respect to UV-C exposure in terms of physicochemical properties, breathability, and bacterial filtration performance. Information on the effect of time-dependent passive decontamination at room temperature storage was provided. Single and multiple cycles of UV-C sanitization did not adversely affect respirator breathability and bacterial filtration efficiency. This multidisciplinal approach may provide important information on how it is possible to correctly sanitize a face mask and, in case of shortage, safely reuse the face mask.
Face masks provide a physical
barrier to reduce person-to-person
virus or bacteria transmission in exhaled breath, which mostly originates
from the respiratory microdroplets subsequent to sneezing and coughing,[1] and minimize the transmission of infectious diseases
that are airborne or transmitted via respiratory droplets. Face masks
are composed of a series of nonwoven polymeric layers designed to
avoid the passage of bacteria and viruses in both directions thanks
to their tailored pore geometry and large specific surface area.[2]During the initial phases of the current
pandemic COVID-19, a shortage
in surgical mask supply was observed, requiring measures to conserve
face masks after selecting an adequate disinfection method and procedure.[3] Environmental problems that could follow the
actual pandemic period were also to be considered, due to the increase
in production and consumption of face masks across the world.[1,4] Single-use polymeric materials have been identified as a significant
source of plastics and plastic particle pollution in the environment.[5,6] The reuse of COVID-19 face masks after sanitization can be used
as a novel solution to this emerging waste problem,[1,4] which
can facilitate the shift towards an eco-efficient circular economy
within the healthcare industry.Ultraviolet-C (UV) surface disinfection
has attracted tremendous
attention, and many products have become available on the market,
guaranteeing a complete disinfection in a short time.[7−9] Various public places with different levels of contaminated surface
probabilities, from hospitals and healthcare facilities to restaurants
and cafeterias, have started using UV-C surface disinfection systems.
UV-C tools have demonstrated to be effective for microbial disinfection,
and they are preferable to other methods (ozone, thermal treatment,
plasma exposure, γ irradiation, etc), having several advantages,
including rapid effectiveness and absence of chemical residual or
risk exposing the users to toxic chemicals.However, a limited
understanding of the critical aspects of UV-C
disinfection has led to inappropriate use of this promising technology.
Dubious and nonscientific performance claims by some of the UV-C system
designers and manufacturers are unfortunately widespread.[10]Even though UV-C can be used to preserve
our current supply of
filtering face masks through cycles of decontamination and reuse,[11] UV-C radiation can potentially degrade TNT polymer
layers and/or the polymer chemicophysical properties of the fibers;
hence, it could affect the ability of a disposable facemak to protect
the people.[1,7,8,10,12] In addition, soft,
porous, irregular surfaces may present a challenge for UV-C decontamination
due to the potential for areas of shadowing and absorption of organisms
into sites with reduced delivery of UV-C.[13] However, any decontamination process may limit the functionality
of the mask if it alters its fitting and filtering efficiency in terms
of penetration and/or air flow resistance. Detailed studies are needed
in order to analyze this aspect and define a specific protocol.[14]The main aim of the present study is to
provide the necessary information
for developing UV-C devices for bacterial and virus disinfection on
porous filtration materials such as surgical masks during the COVID-19
pandemic and beyond, preserving the polymer properties and face mask
efficiency. The sanitization device was designed to obtain a uniform
UV-C light distribution on the face mask surfaces for a safe sanitization
process in terms of viral abatement and material characteristics.
In order to estimate the irradiance distribution provided by a UV-C
lamp on a three-dimensional (3D) area like the face mask surface,
and in order to design the device in a right and safe way, the use
of DIALux software was evaluated. Previous researchers have applied
the following approaches: Baluja et al.[15] proposed a method to find the best configuration to decontaminate
several masks at once, ensuring the appropriate dosage in shaded zones
by DIALux Evo 8.2 simulations of the irradiance pattern inside a box.
Ropathy et al.[16] reproduced the lighting
in different room layouts in order to evaluate the effectiveness of
a UV light-based surface disinfection system.In the past years,
different decontamination devices have been
developed to sanitize face masks, by applying UV-C light irradiation.[7] Many of these systems do not consider the 3D
structure of the face mask and of the contamination; hence, the real
and complete decontamination cannot be assured. Here, we propose a
device designed to permit a real and safe decontamination of the whole
face mask, with a decontamination cycle defined in terms of exposure
time and irradiance, and we define the number of decontamination cycles
guaranteeing face mask integrity, in order to avoid any physical–chemical
degradation of the face mask properties. The novelty of this interdisciplinary
work lies in its combining the knowledge of different fields (polymers,
virus and bacteria, light distribution, and design), in order to develop
an efficient system and to provide the scientific basis for further
improvement.This study contributes to enabling the reuse of
surgical face masks,
allowing a potential huge reduction of plastic wastes.
Materials and Methods
UV-C Device Design
UV-C Lamps and Measurements
UV-C
lamps produced from a low-pressure mercury light source that emits
short waves at 254 nm were used in this study: 15 Watt Philips, TUV
T8, and 4 Watt Philips TUV 4W. The radiation intensity emitted by
the UV-C lamps was measured and acquired with a radiometric probe
LP471 TVC in the wavelength range between 220 and 280 nm, with a peak
at 260 nm and quartz diffuser for cosine correction. The measuring
range varies between 0.1 × 10–3 and 2000 W/m2.
Mechanical Design of the Sanitization Box
A customized sanitization box was designed and successively prototyped
for the purpose of experimentally testing the sanitization equipment
and protocol on the chosen face masks. The design of the equipment
involved the following phases: (i) a conceptual design of the box
based on the project requirements (e.g., need to guarantee the UV
radiation confinement, need to guarantee the maximum exposure to UV
radiation for both the external and internal surfaces of the face
mask) to derive the functional and modular structures of the device
and, finally, the product concept; (ii) an embodiment and detailed
design of the box exploiting the CAD system SOLIDWORKS 2019 to define
the most appropriate geometrical shapes and materials of all of the
components, and to develop the virtual prototypes; and (iii) a critical
design review phase to optimize the box model (e.g., miniaturization
of the cavity and supports, most appropriate positioning of the internal
component, material selection considering, for instance, the effects
due to radiation reflections). A 3D view of the developed assembly
is reported in Figure .
Figure 1
3D view of the sanitization device, with the lamp protection grid
(red part) and the face mask support (green part).
3D view of the sanitization device, with the lamp protection grid
(red part) and the face mask support (green part).The external box of the device, composed of two
main parts, has
gross dimensions of 244 × 124 × 98. The use of a plastic
material (i.e., polyamide) has been preferred to assure lightness.
As can be seen in Figure , the sanitization lamps are positioned in the central part
at the top and bottom of the box, while in the left and right parts,
specific spaces are dedicated to the housing of electronic devices
and batteries.To cover the two lamps and avoid accidental contacts,
a protection
grid has been designed (the red part in Figure ). The dimensioning of such a component has
been done through a trade-off among two conflicting requirements:
to guarantee a robust protection against physical contacts with lamps,
and to minimally perturbate the UV radiation directed to the mask
surfaces. To this purpose, different prototypes with different dimensions
have been realized (through 3D printing), installed in the sanitization
box, and then tested by measuring the percentage reduction of the
UV-C light within the cavity by means of the radiometric probe LP471
TVC. The best compromise turned out to be a cylindrical protection
grid that encloses the whole lamp, positioned at a minimum distance
from the lamp’s external surface (i.e., 1 mm), with 16 holes
and with rib dimensions of 2 × 2 mm2.Another
important component of the sanitization box is the support
(the green part in Figure ) needed to maintain the face mask in the right position during
the sanitization cycle, assuring to expose to radiation most of the
mask’s internal and external surfaces without creases. The
developed framework has dimensions of 100 × 75 × 18 mm3 (excluding the fixing pins needed to assemble the support
with the box) and it is composed of ribs of dimensions 3 × 3
mm2. As can be seen from the Supporting Information Figure S1, the support is composed of rounded
ribs and has a draft angle of 18.5° to favor the face mask positioning
and removal (less than 1 min for each operation), so that the upper
part has external dimensions of 100 × 65 mm2.
Irradiance Simulation
To ensure
proper decontamination, it is crucial to study, simulate, and estimate
the irradiance distribution on the face mask surface provided by the
lamps and evaluate the right lamp/mask distance to assure a safe sanitization
procedure in a short time. The software DIALux Evo 9.2[17] was used to this aim; this tool is commonly
used for architectural lighting and for the design of indoor, outdoor,
and street lighting systems. Here it was applied to the UV-C light
distribution. In particular, the followed methodology derives from
previous research studies,[15,16,18] where a correlation between Lux (lx) (output of the simulations)
and the UV-C intensity in μW/cm2 was established.
In the present paper, the correlations found from Arines[15,18] were taken into account: in order to get the isolines in μW/cm2, it is necessary to multiply by 100 the radiant flux of the
lamps in W, before introducing the value-correspondent item of the
tool.Furthermore, in order to validate the used method and
to define the right photometric solid distribution of the lamp, preliminary
photometric measurements, by radiometric probe, were carried out in
a parallelepiped box internally covered with aluminum (internal dimensions
55 × 24 × 15 cm3) and with a UV-C lamp inside
(Philips TUV T8, total power of 15 W and UV-C radiation power of 4.9
W); the measured values were compared with the simulation results.
Different test surfaces were identified with the UV-C lamp disposed
along the longer dimension (55 cm) in all of the configurations. In
DIALux models, two parameters control the way in which light reflects
on the walls: a coefficient of 73% was chosen for the metallic surface
of the walls (reflectance factor), and a value of 50% was chosen for
the reflective coating.[15,16,18] The lighting spatial distribution of the lamp’s irradiance,
defined thanks to these measurements, was used for the definitive
model of the UV-C disinfection device. Figures S2 and S3 in SI show the models of the tested boxes developed
in DIALux: in Figure S2 the preliminary
box, and in Figure S3 the final UV-C-based
disinfection device. Figure represents the characteristics of the photometric solid distribution
of the UV-C selected lamp: it was chosen based on the preliminary
tests.
Figure 2
UV-C germicidal lamp: photometric spectrum (maximum emission at
250 nm), and the selected photometric spatial distribution (emitted
candle for kilolumen of the lighting flux).
UV-C germicidal lamp: photometric spectrum (maximum emission at
250 nm), and the selected photometric spatial distribution (emitted
candle for kilolumen of the lighting flux).The final project of the disinfection box (Figure ) was modeled in
AutoCAD and imported in
DIALux. The same boundary conditions were assumed for the input power
of the lamps and the features of the devices’ casing. In this
final configuration, the mask was schematically represented by means
of three rectangular surfaces that are placed between the two lamps
(Figure ).
Figure 3
(a) 3D view
of the calculation surfaces inside the box; (b) the
two-dimensional (2D) and 3D maps of the simulated irradiance values
inside the device.
(a) 3D view
of the calculation surfaces inside the box; (b) the
two-dimensional (2D) and 3D maps of the simulated irradiance values
inside the device.
Surgical Face Mask
Commercial-grade
surgical face mask were selected for this study. Face mask are based
on three layers of nonwoven fabric microstructures of thermoplastic
polymers: the external and internal layers are based on spunbond poly(ethylene
terephthalate) (PET), while the internal layer is based on melt-blown
poly(butylene terephthalate) (PBT).
Sanitization Evaluation
Artificial Contamination of Type II Surgical
Masks with ϕ6 as the Biological Indicator
The artificial
contamination was performed to achieve massive contamination of the
mask. A suspension of ϕ6 with a concentration of ≈109 PFU/mL was aerosolized for 2.5 min on each side of the mask.
The mask was placed in the Andersen impactor connected to a vacuum
pump with a flow rate at 28.3 L/min, permitting the aerosolized virus
to reach directly the mask.
ϕ6
Bacteriophage ϕ6
DSM21518 derives from the microbial collection of the Leibniz Institute
DSMZ-German Collection of Microorganisms and Cell Cultures GmbH (Braunschweig,
Germany), and was propagated using the double-layer agar method. The
lower layer consists of Trypticasein Soy Agar (TSA, Condalab) and
the upper layer consists of 5 mL of Trypticasein Soy Broth (TSB, Condalab)
supplemented with 0.9% agar (Difco) mixed with 100 μL of Pseudomonas syringae (DSM21482) incubated overnight
at 28 °C in TSB. Subsequently, after pouring the soft agar, 100
μL of bacteriophage solution ϕ6 was inoculated by spot.
The plates were then incubated overnight at 28 °C. The plaque
formed, ϕ6, was recovered with 4 mL of viral buffer (Na2HPO4 7 g/L, KH2PO4 3 g/L,
NaCl 5 g/L, 1 mM MgSO4, 1 mM CaCl2). After the
viral buffer was added, the plate was stirred at 50 rpm for 4 h, at
the end of which the soft agar was scraped and purified by centrifugation
at 6000 rpm for 5 min to separate the host cell particulate and bacteriophage.
The supernatant was filtered through a 0.22 μm Millex-GP syringe
filter unit and used as stock. Stocks in glycerol and DMSO (10% vol/vol)
were prepared of the ϕ6 solution, stored at −80 °C.
Real Contamination
The masks were
worn for periods between 2 and 4 h by different operators to contaminate
the mask with a microbiological population as much representative
as possible in terms of quantity and quality.
Bioburden Test and Disinfection Efficiency
The bioburden test (according to standard EN 14683:2019[19]) was used to estimate the totally viable microorganisms
present on the sample before (for the control) and after the sanitization
treatment. The mask was inserted into the bottle (Duran Schott, Mainz-Germany)
containing the extraction liquid (viral buffer for ϕ6 contamination:
Na2HPO4 7 g/L, KH2PO4 3
g/L, NaCl 5 g/L, 1 mM MgSO4, 1 mM CaCl2; peptone
water for natural contamination: peptone 1 g/L, NaCl 5 g/L, surfactant
polysorbate 20 2 g/L). It was then stirred for 5 min at 250 rpm. At
the end of incubation, the quantification of the virus was evaluated
by counting the lysis plaques; each lysis plate is defined as a plaque
forming unit (PFU) and corresponds to a virion unit. Several aliquots
of extraction liquid together with 100 μL of P. syringae and 6 mL of 0.90% soft agar in sterile
20 mL tubes were after a little mixing poured onto Petri dishes containing
TSA. The plates were incubated for 24 h at 28° C. In the case
of natural contamination, after the incubation, several aliquots (1–100
mL) of the liquid were filtered through a sterile 0.45 μm microbiological
filter (Whatman) by using a filtration system (CombiSart Multi-Branch
System, Sartorius, Germany). The filter was then placed on Petri dishes
(Ø60 mm) of TSA for quantification of the bacteria, and Saboraud
agar (SDA) was for quantification of the fungi; the plates were incubated
for 24 h at 37 °C and for 48/72 h at 28 °C. After incubation,
the quantification of colony-forming units (CFUs) and PFUs and the
disinfection efficiency were evaluated by means of eqs and 2wherewhereCFU or PFU = colony-forming units (plaque forming units) found
on the filterV = filtered volume (or
spread volume)VTOT = total volume of extraction
liquid (viral buffer or peptone water)Ab. Log = logarithmic abatementC = UFC found on a mask exposed to
UV radiationC0 = UFC found on untreated
mask (control)
UV-C Sanitization Effect on Face Mask Materials
To study the effect of UV-C irradiation on polymeric TNT material
properties, the face masks were irradiated with 20, 40, 60, 80, and
100 J/cm2 of UV-C radiation, and the material characterization
results were compared with the non-irradiated masks in terms of infrared
spectroscopy, wettability, and morphology.
Infrared Spectroscopy
The face
masks’ TNT nonwoven fabrics were chemically characterized
by Fourier infrared spectroscopy (FT-IR) in the 400–4000-cm–1 range by a Jasco FT-IR 615 spectrometer. Pristine
and sanitized face masks were analyzed in ATR mode with a germanium
crystal.
Water Contact Angles (WCA)
The
water contact angles (WCA) were assessed using the sessile drop method
in air by an FTA1000 Analyzer (Dinwiddie Street, Portsmouth, VA).
Deionized water drops of 20 μL (high-performance liquid chromatography
grade water) were placed on the face mask, and measurements were recorded
10 s after the liquid made contact with the surface. Five independent
determinations at different sites were averaged. Neat and exposed
face masks were analyzed.
Morphological Analysis
The morphological
analysis of the surfaces of the spunbond and melt-blown TNT and of
the fracture sections before and after sanitization was carried out
by means of scanning electron microscopy (SEM) measurements, using
the SEM Jeol instrument JSM 5200. Before analysis, all of the samples
were metallized with gold, using the Balzers MED010 instrument. Furthermore,
the sections were made after freezing the samples.
Breathability and Bacterial Filtration Efficiency
(BFE)
The effect of multiple disinfection cycles on the face
mask integrity was analyzed in terms of breathability and BFE. The
breathability measurements were performed according to the UNI EN
14683:2019 standard[19] using the GBN701
differential pressure tester. To carry out the measurements, the masks
were deprived of the rubber bands and cut laterally so that the fabric
is stretched out without creases. The measurement was repeated on
five distinct points representative of the entire mask and the breathability
was measured on each point of the masks.The BFE was measured
as described in UNI EN 14683:2019 standard,[19] modified by using the Escherichia coli ATCC 9637 as the model organism. A suspension of E. coli was aerosolized using a nebulizer (Xearpro
Bulldog Aero) through a pyrex glass aerosolization chamber (680 mm
80 mm) attached to a 6-stage Andersen impactor (TE-10–800 Tisch
Environmental) connected to a vacuum pump with a flow rate at 28.3
L/min. The bacterial suspension concentration was adjusted to provide
a value of 1700–2700 colony-forming units (CFUs) in the positive
control test (without mask). A specimen of the mask material was clamped
between a six-stage cascade impactor and an aerosol chamber. The BFE
of the mask is given by the number of colony-forming units passing
through the medical face mask material and expressed as a percentage
of the number of colony-forming units present in the challenge aerosol
according to eq
Results and Discussion
Irradiance Measurements and Simulation Results
Figure S4 shows the results of the simulations
performed on the rectangular-shaped test box. The irradiance isolines
obtained from the simulations are represented: the red points correspond
to the measurement positions and in black the measured values are
shown. For the first lighting distribution (Figure S4a), at a distance of about 15 cm, the measured irradiance
values are similar to the simulated values only under the lamp, whereas
the distribution of the irradiance has an opposite behavior in comparison
with the measurements, with a difference of up to 30%. The photometric
solid is not appropriate and a second one was therefore considered:
a better correspondence between the measurements and the program outputs
is observed in this case (Figure S4b) with
maximum differences of about 3–4%. Based on these results,
the second type of UV-C-wave germicidal tube with a larger and flattened
spatial distribution showed a suitable irradiance behavior, and it
was selected to study the UV-C light arrangement for the disinfection
device (Figure ).The final configuration with a lower total volume of the device,
an aluminum internal surface, and two lamps symmetrically disposed
allows a more uniform distribution of the irradiance on the sanitized
surfaces. Without supporting grids, both measurements and simulations
were carried out. A good correspondence above all in the central surface
of the mask was obtained (2200–3000 μW/cm2 measured vs 2600 μW/cm2 simulated), with maximum
differences of about 13–15%. With the supporting grids of the
lamps, a uniform value of 2100 μW/cm2 is obtained
in the central area of the mask (surface n.2); values of 1100–1000
μW/cm2 are obtained in the border-bent zones (surfaces
n.1 and n.3), as shown in Figure .
Figure 4
Image of the final sanitization
device.
Image of the final sanitization
device.The simulation results of the box with the face
mask support yielded
a radiation intensity of about 2000 mW/cm2 at the distance
of about 1.5 cm. The resulting radiation dose, the main parameter
to be considered in the surface sanitization procedure, can be determined
by eq Hence, by modulating the exposure time a radiation
dose ranging from 1.2 J/cm2 (10 min) to 3.6 J/cm2 (30 min) can be obtained in the sanitization device. Studies in
the literature[13] have shown that a dose
of more than 1 J/cm2 is needed to guarantee a good level
of decontamination.
Sanitization Box Prototype
According
to the illuminotechnical simulation results, the sanitization box
prototype was designed with the following geometrical and material
characteristics:External dimensions: 244 × 124 × 90 mm3Dimensions of the internal cavity:
157 × 115 ×
65 mm3Lamp + supports dimensions:
155 × 20 × 25
mm3Lamp position: centered
in the internal cavityDistance between
the lamp surface and mask surface:
15 mmThe main functional groups composing the prototype are
the following:a plastic box composed of the main body and a cover,
joint through two metallic hinges that allow the opening and closing
of the sanitization box. The internal surface of the box has been
entirely covered with a 0.5 mm thick aluminum layer in order to maximize
the reflections of the UV-C radiation, and thus guarantee an as-uniform-as-possible
distribution within the sanitization cavity, as used in the DIALux
simulation tool;an interlock that avoids
the lamp power up when the
cover is not completely closed, satisfying the safety requirements
during the device use;two lamp protection
grids realized in polycarbonate
through a 3D printer;a face mask support
realized in polycarbonate through
a 3D printer;a lighted button integrating
a light-emitting diode
(LED) able to light up in four different colors (blue, green, yellow,
and red) to indicate four different device states (stand-by, ready
to be used, sanitization in progress, and alarm).Figure shows the
image of the prototyped sanitization device.
Sanitization Effects
Bacteriophage
ϕ6 has been chosen as a biological indicator to test the optimal
exposure dose for one sanitization cycle to be able to obtain a 3-log-reduction
of the viral load. Use of enveloped viruses like bacteriophage ϕ6
is desirable because it may capture the potential effects of a viral
envelope on the virus’s interaction with its environment, such
as on a surface or in aerosol, which may impact the UV disinfection
performance.[20] Moreover, the behavior of
ϕ6 under UV-C irradiation has been described in detail and compared
with the Sars COV virus,[21] appearing more
resistant with respect to other enveloped viruses, thus suggesting
ϕ6 as a practical and realistic conservative virus surrogate
where use of coronaviruses is not feasible. According to Nicolau et
al.,[22] no study on UV irradiation on surgical
masks have reported the use of ϕ6 as a biological indicator;
conversely, it was recently used on N95 respirator UV-C disinfection
protocols.[7,23,24]Masks
artificially polluted by ϕ6 aerosolization resulted in a viral
dose of ca 106 PFU/mask, while masks really polluted by
wearing by several operators in different indoor and outdoor environments
resulted in a bacterial load of ca 105 CFU/mask.Figure shows the effect of different UV-C doses on log abatement
of real and ϕ6 contamination on surgical masks. During this
experiment, a limited reduction of microbial load was observed (up
to −1.4 LOG) even with a high UV dose in both typologies of
contamination. Besides the small reduction, increasing doses of UV
irradiation did not retrieve an increasing reduction of residual microbial
load after the UV treatment, thus indicating some limitation in the
UV irradiation effect.
Figure 5
Biological agent abatement under different UV-C doses
on surgical
masks subjected to real (□ symbol) and ϕ6 (x symbol)
contamination using a prototype without face mask support.
Biological agent abatement under different UV-C doses
on surgical
masks subjected to real (□ symbol) and ϕ6 (x symbol)
contamination using a prototype without face mask support.The data underlined the shadowing as one of the
main setbacks for
UV-C’s sanitization method; this problem occurs when parts
of the masks are poorly irradiated, and the object possesses inner
layers where microorganisms can remain. This aspect is claimed as
one of the main drawbacks able to impact UV-C’s germicidal
capability.[22] An upgraded version of the
prototype has been developed to address this limitation, including
a face mask support, accurately designed in order to overcome these
problems and able to keep open the whole mask’s superficial
area (the green part in Figure ).Figure shows the effect of different UV-C doses
on the log-reduction
of real and ϕ6 contamination on surgical masks by applying the
upgraded prototype, integrated with a specific face mask support (Figure S1). The values on the x-axis show the
irradiance dose obtained by applying the simulated UV-C value to the
exposure time.
Figure 6
Biological agent abatement under different UV-C doses
on surgical
masks subjected to real (□ symbol) and ϕ6 (x symbol)
contamination using an upgraded version of prototype with face mask
support.
Biological agent abatement under different UV-C doses
on surgical
masks subjected to real (□ symbol) and ϕ6 (x symbol)
contamination using an upgraded version of prototype with face mask
support.According to the mechanical design of the sanitization
box and
the biological results that permitted to study the effect of different
UV-C doses on the log-reduction of real and ϕ6 contamination,
the sanitization protocol was set to guarantee a log abatement value
of 3 corresponding to a 30 min long cycle of irradiation, which according
to radiometric probe measurements is equal to a 2.8 J/cm2 irradiance dose. These data are in accordance with the recently
published results.[13]
Face Mask Properties Analysis
Face
mask polymeric properties were tested in terms of infrared spectroscopy,
wettability, and microstructure, after exposure to increased irradiance
UV-C values, from 20 to 100 J/cm2, which are comparable
from 7 to 35 sanitization cycles, respectively.Infrared
spectra (Figure ) show the typical characteristics of the
absorption spectra of the neat PBT polymer: i.e., 3000–2800
cm–1; for the C–H aliphatic stretching vibration
of saturated and unsaturated compounds, the C=O vibrational
band at around 1716 cm–1, the symmetric and asymmetric
C-O-C stretching modes in the 1200–1100 cm–1, spectral range, and modes assigned to the aromatic ring at 870
and 725 cm–1 are found. After UV-C exposure, no
pronounced changes in the molecular structure of PBT under the conditions
studied are observed. In the region 1600–1700 cm–1, some new bands near the C=O peak could be observed, which
are attributed to the formation of degradation byproducts, including
conjugated aldehydes and conjugated ketones, due to the degradation
and oxidative effects of UV-C radiation. This band is evident only
after 80 J/cm2 exposure; it increases with irradiation
time[25,26] and is due to the photoproducts of PBT.[27] The band at 1690 cm–1 is not
evident for the lower UV-C dose irradiance. Different studies have
proposed that the photo-oxidation mechanism of PBT involves the formation
of ester derivatives, perester derivatives, aliphatic acids, benzaldehyde,
and benzoic acid in the presence of oxygen.[26]
Figure 7
Infrared
spectra in the ATR spectra mode of the unexposed and exposed
external layers of surgical face masks after increased irradiance.
Infrared
spectra in the ATR spectra mode of the unexposed and exposed
external layers of surgical face masks after increased irradiance.
Wettability
Figure shows the water contact angle images and values of pristine
and UV-C-treated TNT surface with 80 and 100 J/cm2. TNT
nonwoven fabrics, used to develop surgical face masks, have hydrophobic
properties. Wettability and droplet adherence are important properties
that were expected to provide an indication about the likelihood of
droplet transmission through face masks. The selected TNT shows a
WCA of 109°; the exposure to UV-C radiation for a short time
does not modify this value; in fact, TNT exposed to 80 J/cm2 has the same WCA value. By increasing the irradiance dose, a decrease
of the WCA can be observed. A reduction of 30% was measured at 100
J/cm2; this reduction is confirmed by the infrared analysis,
performed in ATR mode. The surface wettability of PBT measured by
the contact angle is modified by the irradiation.[28] The surface photo-degradation increases the water wettability
of the initially hydrophobic polymers. A shorter irradiation dose
could not modify the surface. UV-C irradiation of PBT under air atmosphere
could generate new functional groups, such as lactones, aldehydes,
and anhydrides, that better interact with the water molecules, showing
a decreased WCA.
Figure 8
WCA angle images and values of unexposed and exposed external
layers
of surgical masks after increased irradiance dose.
WCA angle images and values of unexposed and exposed external
layers
of surgical masks after increased irradiance dose.It is known that aromatic polyesters exposed to
UV light, in vacuum
or inert atmosphere, undergo photo-degradation and/or photo-cross-linking
reactions. Irradiation of PBT at 254 nm results in the formation of
benzoic acid, benzaldehyde, formate, and alcohol end groups via Norrish
I mechanisms, and benzoic acid, vinyl, and γ -butyrolactone
end groups via Norrish II mechanisms. All of these functions have
been previously identified by IR spectroscopy.[26]Figure shows the SEM images of the internal meltblow layer of a
surgical face mask, by comparing the pristine materials with those
exposed to 100 J/cm2 UV-C radiation. The internal polymeric
layer comprises small voids compared to the other two layers and it
acts as a filter, stopping harmful and unwanted particles from entering
the body.[1] The microstructure of the layer
is an important parameter to consider since the porosity and surface
area of the fibers in the face mask dictate their breathability and
filterability. The SEM images did not demonstrate any observable change
of the general structure of the surgical masks. UV-C did not damage
the filtration layer even when the exposure time was up to 100 J/cm2. Although UV-C is proven to facilitate the degradation of
thermoplastic polymers, a short exposure targeted at disinfection
of the mask would not cause significant structural damage to the filtration
layer.[29]
Figure 9
SEM images of the internal meltblow layer
of a surgical face mask
at different resolutions of unexposed (A) and exposed surface at 100
J/cm2 (B).
SEM images of the internal meltblow layer
of a surgical face mask
at different resolutions of unexposed (A) and exposed surface at 100
J/cm2 (B).
Breathability and BFE
To investigate
whether UV-C exposure in air affects the medical face mask’s
efficiency, breathability and bacterial filtration efficiency were
analyzed, after single and multiple sanitization cycles. Table shows the breathability
and BFE values on the original face mask and after one and five sanitization
cycles. Five cycles were selected in order to obtain a maximum irradiance
dose of less than 20 J/cm2, which was proven to not modify
the infrared spectra, morphology, and wettability of the TNT polymeric
tissue, and to safely decontaminate the face masks. Table underlines that the face mask
efficiency in terms of breathability performances (resistance to air
flow) and bacterial efficiency penetration were not significantly
affected regardless of the UV-C decontamination process until 5 cycles
of decontamination. Compared with untreated masks, both values remained
within the variability range of measurements made on the untreated
masks. Variation in these measurements is mainly due to the intrinsic
local heterogeneity of the fibrous structure composing the filter
tissue of the masks. Thus, we can conclude that the defined sanitization
multiple cycle does not alter the structure of the nonwoven media.
Table 1
Breathability and BFE Values of the
Face Masks, after Single and Multiple Sanitization Cycles, Compared
with the Original Ones
face mask
breathability (Pa/cm2)
BFE (%)
original
46.2 ± 0.9
99.95 ± 0.05
1 cycle
46.0 ± 1.2
99.92 ± 0.03
5 cycles
46.7 ± 1.1
99.85 ± 0.09
Conclusions
Decontamination of surgical
masks has become an alternative strategy
to regenerate basic protective equipment so as to control the spread
of diseases under the current difficult situation. In the present
research, ultraviolet germicidal irradiation has been demonstrated
to have potential for use in disinfecting medical face masks, which
could allow the mask to be used safely multiple times during a public
health emergency. However, we demonstrated the importance of designing
specific support in order to assure a real and uniform UV-C distribution
on all face mask surfaces. DIALux software was successfully applied
to simulate and study the spatial distribution of the UV-C light on
the different surfaces of the face masks.Furthermore, it is
important to understand how UV-C affects the
polymeric layer of the mask, and especially whether UV-C degrades
the protection offered by the respirator. Our results suggest that
UV-C could be used to effectively disinfect disposable masks for reuse,
but the maximum number of disinfection cycles will be limited and
connected to the UV-C dose required to inactivate the pathogen. Our
results demonstrate that we can safely decontaminate face masks for
almost 5 times, without affecting the face mask performance in terms
of breathability and bacterial filtration efficiency and surface polymeric
properties in terms of microstructure, wettability, and chemical properties.
Our device, methodology, and sanitization protocol, if put into practice,
can provide several innovative ideas that we believe represent meaningful
contributions to the field of UV-C decontamination devices. We have
proven that the lifetime of medical face masks can be extended. This
multidisciplinal approach provides important information on how often
a given face mask may be safely reused.
Authors: Krista R Wigginton; Peter J Arts; Herek L Clack; William J Fitzsimmons; Mirko Gamba; Katherine R Harrison; William LeBar; Adam S Lauring; Lucinda Li; William W Roberts; Nicole C Rockey; Jania Torreblanca; Carol Young; Loïc G Anderegg; Amy M Cohn; John M Doyle; Cole M Meisenhelder; Lutgarde Raskin; Nancy G Love; Keith S Kaye Journal: Open Forum Infect Dis Date: 2020-12-15 Impact factor: 3.835