Synthesis and Decontamination Effect on Chemical and Biological Agents of Benzoxonium-Like Salts

Benzoxonium chloride belongs to the group of quaternary ammonium salts, which have been widely used for decades as disinfectants because of their high efficacy, low toxicity, and thermal stability. In this study, we have prepared the C10-C18 set of benzoxonium-like salts to evaluate the effect of their chemical and biological decontamination capabilities. In particular, biocidal activity against a panel of bacterial strains including Staphylococcus aureus in biofilm form was screened. In addition, the most promising compounds were successfully tested against Francisella tularensis as a representative of potential biological warfare agents. From a point of view of chemical warfare protection, the efficiency of BOC-like compounds to degrade the organophosphate simulant fenitrothion was examined. Notwithstanding that no single compound with universal effectiveness was identified, a mixture of only two compounds from this group would be able to satisfactorily cover the proposed decontamination spectrum. In addition, the compounds were evaluated for their cytotoxicity as a basic safety parameter for potential use in practice. In summary, the dual effect on chemical and biological agents of benzoxonium-like salts offer attractive potential as active components of decontamination mixtures in the case of a terrorist threat or chemical or biological accidents.


Introduction
Benzoxonium chloride (N-benzyl-N,N-bis(2-hydroxyethyl)dodecan-1-aminium chloride, BOC), known for over 30 years [1], manifests strong antimicrobial activity against certain bacterial strains, especially non-spore forming, yeasts and protozoa. In practice, BOC is widely used against buccopharyngeal pathogens as a mucous membrane disinfectant. It is commercially available in the form of gargle solutions, lozenges, and oral sprays, often in combination with lidocaine [2,3]. Likewise in dentistry it is used against dental plaque and dental caries [4,5]. Further applications include disinfection of medical instruments in hospitals, and of skin burns, seborrheic dermatitis, and cutaneous leishmaniosis [4,6,7], as a veterinary fungicide and bactericide in the treatment of animal skin, in the food and beverage industry, and in the textile industry as a bactericide in textile pounds were fully characterized by NMR spectra and HRMS. NMR spectra were recorded on a Varian VNMR S500 (operating at 500 MHz for 1 H and 125 MHz for 13 C; Varian Co., Palo Alto, CA, USA). The chemical shifts (d) are given in ppm, relative to tetramethylsilane (TMS) as internal standard. Coupling constants (J) are reported in Hz. Splitting patterns are designated as s, singlet; d, doublet; t, triplet; and m, multiplet. Mass spectra were recorded using a combination of liquid chromatography and mass spectrometry: highresolution mass spectra (HRMS) and sample purities were obtained by high-performance liquid chromatography (HPLC) with UV and mass spectrometric (MS) detection gradient method. The system used in this study was a Dionex Ultimate 3000 UHPLC: RS Pump, RS Column Compartment, RS Autosampler, Diode Array Detector, controlled by Chromeleon (version 7.2.9 build 11323) software (Thermo Fisher Scientific, Germering, Germany) with Q Exactive Plus Orbitrap mass spectrometer with Thermo Xcalibur (version 3.1.66.10.) software (Thermo Fisher Scientific, Bremen, Germany). Detection was performed by mass spectrometer in positive mode. Settings of the heated electrospray source were: Spray voltage 3.5 kV, Capillary temperature: 262 • C, Sheath gas: 55 arbitrary units, Auxiliary gas: 15 arbitrary units, Spare gas: 3 arbitrary units, Probe heater temperature: 250 • C, Max spray current: 100 mA, S-lens RF Level: 50. C18 column (Kinetex EVO C18, 3 × 150 mm, 2.6 µm, Phenomenex, Torrance, CA, USA) was used in this study. Mobile phase A was ultrapure water of ASTM I type (resistivity 18.2 MΩ.cm at 25 • C) prepared by Barnstead Smart2Pure 3 UV/UF apparatus (Thermo Fisher Scientific, Bremen, Germany) with 0.1% (v/v) formic acid (HPLC-MS grade, Sigma Aldrich, Steinheim, Germany); mobile phase B was acetonitrile (MS grade, Honeywell-Sigma Aldrich) with 0.1% (v/v) of formic acid. The flow was constant at 0.4 mL/min. The method started with 1 min of isocratic flow of 5% B, and then the gradient of B rose to 100% B in 3 min and remained constant at 100% B for 1 min. The composition then went back to 5% B and equilibrated for 5 min. Total runtime of the method was 10 min. The column was heated to 27 • C. Samples were dissolved in methanol (LC-MS grade, Fluka-Sigma Aldrich) at a concentration 1 mg/mL and sample injection was 1 µL. Purity was determined from UV spectra measured at wavelength 254 nm. HRMS was determined by total ion current spectra from the mass spectrometer collected at resolution of 140,000 in a range 105-1000 m/z. Clog P was calculated with the MarvinSketch (version 14.9.8.0) software.
2.1.1. General Procedure for Synthesis of N,N-bis(2-hydroxyethyl)-N-alkylamines (3a-e) Diethanolamine (1) (22.5 mmol), anhydrous potassium carbonate (30 mmol), and potassium iodide (3 mmol) were dispersed in 40 mL of acetonitrile. Subsequently, the appropriate 1-bromoalkane 2a-e (15 mmol) was added. The reaction mixture was refluxed under nitrogen atmosphere for 12 h. After filtration the acetonitrile was evaporated under reduced pressure. The residue was dissolved in water (30 mL) and extracted twice with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, filtered, and evaporated to obtain a yellow oily product in 65-96% yields. The intermediates 3a-e were of satisfactory purity for the next reaction step (>95%).
All spectra are available in the Supplementary Materials (Figures S1-S15).

Conductivity
The conductivity of surfactant solutions was measured in triplicate on a Tristar Orion conductivity meter in a conductivity cell 013005MD (Thermo Scientific, Waltham, MA, USA). The apparatus was controlled with the software Navigator 21 (Thermo Scientific) using continuous data collection. The solutions were temperature-controlled to 49 ± 0.1 • C. The surfactant stock solutions had a range of concentrations of 15-200 mM and these stock solutions were diluted further to determine the CMC. A linear pump Lineomat (VEB MLW Labortechnik Ilmenau, Germany) was used with a flow rate of 0.43 mL/min. An AREX stirrer (VELP Scientifica Srl, Usmate, Italy) was used for continuous agitation, and the conductivity was recorded every 3 s. The resulting data were captured into an MS Excel datasheet for subsequent analysis. The transformation of the time axis to a concentration axis was performed according to the parameters defining the measurements (starting volume of a liquid in the titration vessel, the concentration of the surfactant solution in the syringe, and the solution feed rate): where C t = concentration at time t, C 0 = starting concentration of the surfactant, V start = volume of distilled water at start, v inj = surfactant solution dosing rate and t = time recorded by Navigator21

Micellar Catalysis
A solution of fenitrothion (O,O-dimethyl O-(3-methyl-4-nitrophenyl) phosphorothioate) was diluted with methanol to obtain a concentration of 10 −2 M (10 mM). The surfactant stock solutions were diluted in distilled water with a concentration of 500 mM, 100 mM, or 10 mM (pursuant to the value of their CMC). Furthermore, these solutions were diluted in the range of concentrations of 10 −1 -10 −5 M. Carbonate buffer 0.1 M was adjusted to pH 10 or 11. Carbonate buffer 250 µL, surfactant stock solution 250 µL, and the solution of fenitrothion 10 µL were homogenized in a 1 cm thick cuvette. The absorption changes were measured by Helios α spectrophotometer (Thermo Fisher Scientific) with a set wavelength of 394 nm. The measurement was temperature-controlled to 37 ± 0.1 • C and stopped at the time when the difference between adjacent absorptions was minimal. The resulting data were processed in Thermo Scientific Vision software (Thermo Fisher Scientific) and then converted into MS Excel. The rate constant was calculated by the procedure described by Guggenheim [25], with modification introduced by Zajicek and Radl [26]. The procedure used is based on the acceptance of the following equation: where A t+∆t = absorption at time t+∆t, A t = absorption at time t, exp = base of natural logarithm, k obs = observed rate constant, ∆t = time between two successive measurements and A n = absorption at infinite time This relationship is a linear equation with slope exp(k obs × ∆t) and intersection A n × (1-exp(-k obs × ∆t)). Data from ten minutes' measurement were put in two columns of MS Excel so that the second column was shifted one row up. This shift presents one value ∆t. Data prepared in such a way were displayed in an XY scatter chart. A trends line with a print-out of the coefficient regression equation was interlaid through the displayed points. The slope thus obtained was used for the calculation of the rate constant k obs from the term exp(k obs × ∆t). Rate constants were recalculated to the reaction halftimes [27].

Bacterial Strains
In vitro antibacterial activity of the prepared compounds was tested on a panel of four Gram-positive and four Gram-negative bacterial strains: Staphylococcus aureus (C1947), methicillin-resistant Staphylococcus aureus (C1926), Staphylococcus epidermidis (C1936), vancomycin-resistant Enterococcus (S2484), Escherichia coli (A1235), extended-spectrum β-lactamase (ESBL) non-producing Klebsiella pneumoniae (C1950), ESBL-producing Klebsiella pneumoniae (C1934), and multi-resistant Pseudomonas aeruginosa (A1245). All named bacteria used in the study were obtained as clinical isolates from patients (University Hospital, Hradec Kralove, Czech Republic) and stored at −70 • C in the cryobank according to the manufacturer's instructions. When needed, each bacterial strain was inoculated and cultivated on Mueller-Hinton agar (HiMedia, Cadersky-Envitek, Prague, Czech Republic). Francisella tularensis LVS, live vaccine strain, was obtained from the collection of Faculty of Military Health Sciences, University of Defense (Hradec Kralove, Czech Republic) and cultured on McLeod plates.

Biofilm Cultivation
The second-subculture colonies of S. aureus were suspended in Mueller-Hinton broth (MHB) to reach 1.0 McFarland Standard. This suspension was diluted with MHB medium 1:30 and subsequently used as the inoculum. The initial bacterial number of the inoculum was verified by viable cell counting and equaled approximately 10 7 CFU/mL. Each well from the MBEC microtiter plate (Innovotech, Edmonton, AB, Canada) was inoculated with 150 µL of inoculum. The inoculated device was incubated for 24 h at 35 • C ± 1 • C while being shaken at 110 rpm. For every MBEC assay, the formed biofilm was verified by viable cell counting of disrupted biofilms after removing four pegs from the lid, rinsing and sonication (Bandelin Sonorex, Bandeline Electronics, Berlin, Germany) in MHB for 15 min. The established bacterial number in formed biofilms equals approximately 10 7 CFU/mL.

Broth Microdilution Method
The antibacterial susceptibility against bacteria was determined by the broth microdilution method according to standard M07-A10 [28]; the optimized protocol has been published previously [29,30]. Mueller-Hinton broth (Merck, Prague, Czech Republic) adjusted to pH 7.4 (±0.2) was used as the test medium. Dimethyl sulfoxide (DMSO) served as a diluent for all compounds and its final concentration did not exceed 1% in the test medium. The wells of the microdilution tray contained 200 µL of the MH broth with twofold serial dilutions of the compounds (500-0.49 µmol/L) and were inoculated with 10 µL of the bacterial suspension. The bacterial suspensions were controlled densitometrically to reach 1.5 × 10 8 viable colony forming units (CFU) per 1 mL. The MIC values, defined as 95% inhibition of bacterial growth, were determined after 24 h and 48 h incubation at The MBC values were determined as the concentration of compound causing a decrease in the number of bacterial colonies by ≥99.9%, after subculturing of a 10 µL aliquot of each well without visible growth.

Flow Cytometry Assay
F. tularensis LVS bacterial suspension in PBS was prepared from fresh overnight subculture to reach O.D. 1.0 (optic density at 600 nm) which in the case of F. tularensis means 4 × 10 9 CFU (colony forming units)/mL. 1 mL aliquots were centrifuged for 7 min, 7000× g at 4 • C and the supernatant was replaced by 500 µL of the tested compound. After 5 min exposure the treated bacterial suspension was again centrifuged for 7 min, 7000× g at 4 • C and the solution of the tested compound was removed. Cells were re-suspended in 1 mL PBS and stored on ice until flow cytometry measurement. A negative control was prepared from dead bacterial suspension resuspended in PBS (OD 1), where the bacteria had been exposed overnight to 36% formaldehyde. Fresh bacteria cultured overnight on McLeod agar plates were resuspended in PBS (OD 1) and used as a positive control. All samples were diluted 100× in 1 mL of PBS, stained with 1 µL of propidium iodide and 1.5 µL of Syto 9, and incubated in the dark for 15 min. 10 µL of vortexed microspheres were added and samples were properly mixed before measurement. All samples we analyzed with a CyAn ADP Flow Cytometer (Beckman Coulter, Indianapolis, IN, USA). Listmode data were analyzed by Summit v4.3 software (Beckman Coulter). At least three independent experiments were performed.

MBEC Assay
The determination of minimal biofilm eradication concentration (MBEC) against S. aureus was determined using MBEC assay plates (Innovotech) according to the manufacturer's instructions using a modified Calgary method [22]. The biofilm formed on the lid of the MBEC assay microtiter plate was rinsed with saline and inserted on the challenge plate.
Each microtiter challenge plate contained tested compounds serially diluted two-fold in MHB, with sterility and growth controls. After incubation for 24 h at 35 • C ± 1 • C, the lid with treated biofilm was removed, rinsed with saline, and the biofilm was disrupted by sonication. Disrupted biofilm was released into a new microtiter plate with MHB supplemented by 0.5% Tween 80 as an antimicrobial neutralizer. The MBEC was determined after 24 h of incubation at 35 • C ± 1 • by reading OD 600 . The challenge plate was covered with a new, sterile lid and after 24 h of incubation at 35 • C ± 1 • C was used for MIC determination by reading OD 600 .

Antiviral Activity Evaluation 2.7.1. Viruses and Cell Cultures
Murine cytomegalovirus (MCMV) and SARS-CoV-2 virus were used in the experiments. The viral stocks were prepared by infecting susceptible cells. For MCMV, NIH 3T3 cells (murine embryonic fibroblasts) were used, and for SARS-CoV-2 (clinical isolate kindly provided by Assoc. prof. Daniel Ruzek, University of South Bohemia, Ceske Budejovice, Czech Republic), Vero cells CCL81 (African green monkey kidney) were used.
The viral stocks were prepared after virus inoculation of the appropriate cells in a suitable cell culture medium (DMEM with high glucose, containing 10% fetal calf serum, 2 mM glutamine, 100 U/mL penicillin and 100 µg/mL streptomycin). The cells were incubated at 37 • C under 5% CO 2 until 80-90% of cells exhibited cytopathic effect (5-7 days). Following 5 min of centrifugation at 500× g the supernatant was collected and frozen in aliquots at −80 • C.

Virucidal Activity Testing
The virucidal activity of the synthesized agents was evaluated by a quantitative suspension test. Briefly, one part of the virus suspension was mixed with one part of bovine serum albumin (final concentration 0.03%; 'clean conditions' as specified in EN 14476) and eight parts of the novel tested compounds. The mixtures were kept at room temperature for 5 min (exposure time). After the exposure period, the mixtures were serially diluted tenfold with ice-cold DMEM and 100 µL of each dilution were seeded into a 96-well microtiter plate with the appropriate cell and incubated at 37 • C in a 5% CO 2 atmosphere until a cytopathic effect was detected, approximately 5-7 days. Six wells per sample dilution were inoculated. Virus-untreated controls with identical protein concentrations were also tested.
Virus titer was determined using the method of Spearman and Karber and expressed as log 10 TCID 50 /mL [31,32]. According to the European Standard EN 14476 for the virucidal activity of disinfection, a product should demonstrate at least a log 10 reduction of 4 in virus titer, corresponding to 99.99% inactivation [33]. To differentiate between virusinduced cytopathogenic changes and the toxic effect caused by the tested compounds, the cell monolayer was monitored until the end of the virucidal activity testing period for morphological changes after exposure to the disinfectant solution.

In Vitro Cytotoxicity and Selectivity Index
The standard 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT, Merck) cell viability assay was applied according to the manufacturer's protocol on the Chinese hamster ovary cell line CHO-K1 (ECACC, Salisbury, UK) [34]. The cells were cultured according to ECACC recommended conditions and seeded at a density of 8 × 10 3 per well in the 96-well plate. The tested compounds were dissolved in DMSO (Merck,) and subsequently in the Nutrient Mixture F-12 Ham growth medium (Merck) supplemented with 10% Fetal Bovine Serum and 1% Penicillin-Streptomycin (both Merck) so that the final concentration of DMSO did not exceed 1% (v/v) per well. Cells were exposed to the tested compounds for 24 h. The medium was replaced by a medium containing 0.5 mg/mL of MTT and the cells were allowed to produce formazan for approximately 3 h under surveillance. Thereafter, the medium with MTT was removed and the crystals of formazan were dissolved in DMSO (100 µL/well; Ing. Petr Švec-PENTA s.r.o., Prague, Czech Republic). Cell viability was assessed spectrophotometrically by the amount of formazan produced. Absorbance was measured at 570 nm with 650 nm as a reference wavelength on Synergy HT (BioTek, Winooski, VT, USA). The IC 50 value was then calculated from the control-subtracted triplicates using non-linear regression (four parameters) by GraphPad Prism 5.03 or 7.03 software (GraphPad Software, Inc., San Diego, CA, USA). Final IC 50 values including SEM (standard error of the mean) were obtained as the mean of three independent measurements. The selectivity indices of compounds have been calculated as the ration of the cytotoxicity (IC 50 ) and minimum inhibitory concentrations after 24 h (MIC) for all bacterial strains.

Synthesis
The series of alkyl-bis(2-hydroxyethyl)benzylammonium chlorides 5a-e was prepared by the two-step reaction according to Limanov et al. [35]. The reaction process is shown in Scheme 1. Scheme 1. Two-step preparation of benzoxonium-like salts.
Yields, melting points, purity, and Clog P are listed in Table 1. Compound 5b was prepared with a superior yield compared to Chernyavskaya et al. [36], but with inferior yield according to Limanov et al. [35] prepared in the same way. Homologues 5a and 5d were obtained in a yield comparable to that of Stefanovic et al. [37]. The decreased yields are the result of repeated crystallizations to reach satisfactory purity of the final products. Compounds 5c and 5e were reported for the first time.

Conductometry
The critical micelle concentrations (CMC) of the new series of compounds were assessed by a conductometric study performed in aqueous solutions at 49 • C, which takes advantage of the dependency between conductivity change and rising concentration of surfactant. The dependence curve is linear until the unimers of the surfactants can balance the interactions between solution and micelle aggregation. This change is manifested as a breaking of the curve as shown in Figure 1. According to Taube's rule [39], obtained data confirm the dependency of CMC on the elongation of the alkyl chain ( Figure 2). The CMC values (Table 2) are the basic characteristics of surfactants needed for further chemical decontamination measurement.

Micellar Catalysis
Next, the hydrolytic activity against fenitrothion was measured. Because the pesticide fenitrothion contains a 4-nitrophenol group detectable by UV/VIS spectrophotometry, it is a suitable candidate for micellar catalysis investigation as a representative of highly toxic organophosphorus compounds with chemical warfare potential [40]. Reaction of fenitrothion with a micellar catalyst provides 3-methyl-4-nitrophenol, which in alkaline medium creates the yellow-colored nitrophenoxide anion with absorption maximum at 400 nm [27]. This decomposition reaction is monitored by the spectrophotometer. Hydrolytic activity was evaluated in this way using the Guggenheim method for the whole series of synthesized compounds 5a-e as an assessment of chemical decontamination potential (Table 3). This method is applicable in the case of first order or pseudo-first order reactions and enables processing of the data using linear regression [25]. Compound 5d is the most efficient micellar catalyst with half-life 2.3 min at 0.01M concentration, and half-life 2.4 min at 0.005M (pH 11 and 37 • C). In comparison with the spontaneous hydrolysis of fenitrothion (k = 14.00 × 10 −6 , T 1/2 = 808.4 min) under the same conditions, the novel compounds were 60-160 times more effective at pH 11. It is evident that increasing the pH by one unit causes a significant acceleration of the organophosphate degradation. Spontaneous hydrolysis of fenitrothion at pH 10 was so slow that it could not be determined by the given methodology.  The compounds are sorted in descending effect as follows 5d > 5c > 5e > 5a > 5b. Spontaneous hydrolysis (SH) of fenitrothion at pH 11-T 1/2 = 808.4 min; at pH 10 it could not be determined by given methodology.
The rate constants determined in the concentrations below the CMC values were affected by spontaneous hydrolysis at a given temperature, by pH, and the presence of hydroxyl groups hydrolyzing the fenitrothion ester bond. Once the concentration exceeds the CMC, the rate constant noticeably rises. Hydroxyl groups and formed micelles together create a counterion cationic surfactant, and fenitrothion is attracted to the Stern layer where it adopts a favorable orientation for nucleophile access and is finally decomposed [41].
The structure-activity relationship evaluation showed a clear effect of the presence of the hydroxyethyl groups on the rate constant of OP decomposition. Indeed, Figure 3 shows asymptotic dependence between rate constant and concentration for the commercially used compounds with identical length of alkyl chain C 12 at pH 11. Whereas DTMA (N-dodecyl-N,N,Ntrimethylammonium chloride) and BAC (N-benzyl-N,N-dimethyl-N-dodecylammonium chloride), commercially used QAS without hydroxyethyl groups, show poor decontamination effect, DHEMA (N,N-bis(hydroxyethyl)-N-dodecyl-N-methylammonium chloride) containing hydroxyethyl groups shows a significant increase in decontamination effect. Notably, 5b was found to be much superior to all the reference compounds. Finally, we proved the necessity for the hydroxyl groups potentiated by the benzyl moiety for justification of the choice of BOC-like compounds. (N-benzyl-N,N-bis(2-hydroxyethyl)dodecan-1-aminium chloride; green color highlights the positive moiety to increase the decontamination effect. The decrease in activity at high concentrations is due to an excess of surfactant. This so-called empty micelle effect has been previously described [42].

Antimicrobial Activity
To evaluate the biological decontamination potential, in vitro antimicrobial activity of compounds 5a-e was evaluated by the broth microdilution method for four Gram-positive and four Gram-negative bacterial strains. Obtained results are presented as minimum inhibitory concentrations (MICs) after 24 h and 48 h, and the minimum bactericidal concentrations (MBCs) after 24 h (Figure 4). High antibacterial activity was found against the G+ bacteria S. aureus (STAU), methicillin-resistant S. aureus (MRSA), S. epidermidis (STEP), and vancomycin-resistant Enterococcus (VRE). The observed higher susceptibility to the tested compounds of G+ bacteria compared to G-bacteria, as discussed previously, is in agreement with the literature [43,44]. The lowest MIC and MBC values, i.e., the highest effectiveness, was observed for S. aureus. The relationship of alkyl chain length to antimicrobial activity showed that the compounds with C 14 (5c) and C 16 (5d) chains were the most efficient against G+ bacteria. In contrast, the G-bacteria E. coli (ESCO), K. pneumoniae (KLPN-), extended-spectrum β-lactamase-producing K. pneumoniae (KLPN+), and multidrug-resistant P. aeruginosa (PSAE MR) were most susceptible to compounds with shorter alkyl chains, C 12 (5b) and C 14 (5c), respectively. Unsurprisingly, the least efficient against all tested bacterial strains was the compound with the shortest alkyl chain C 10 (5a) [14,29,31]. Compared with the commercially used BAC series, the 5a-e series was comparable at a corresponding alkyl chain length. Individually, 5c and 5b have shown the best activity against S. aureus and E. coli, respectively. According to the MICs and MBCs obtained for the traditional strains, the most efficient derivatives (5b, 5c, and 5d) underwent susceptibility testing against Francisella tularensis Live Vaccine Strain (LVS) by flow cytometry assay ( Figure 5). Although we used a F. tularensis LVS model strain that is attenuated in comparison to the virulent strain, the resistance of this strain is identical to that of the virulent strains. F. tularensis is a Gram-negative, intracellular bacterium which is an important medical challenge. F. tularensis is included in category A on the Centers for Disease Control and Prevention (CDC) bioterrorism agent/disease list for the following reasons [45]: (a) it can be easily disseminated or transmitted from person to person; (b) it results in high mortality rates and has the potential for major public health impact; (c) it might cause public panic and social disruption; and (d) it requires special action for public health preparedness. In view of the above, any substance that can successfully kill F. tularensis is highly desirable. The time of exposure (5 min) and reference compounds (ethanol 70% and BAC 0.1%) were used to simulate more practical conditions. The obtained results showed high efficacy especially of 5b, at least comparable to all reference drugs ( Figure 6). Notably, substance 5b at concentration 0.1% has an even better effect compared to ethanol, which is used as standard for disinfection and decontamination against pathogenic bacteria. Moreover, the effect of alkyl chain length on susceptibility to G-bacteria, represented by decreasing activity from 5b to 5d, corresponded to results obtained by microdilution assay. In addition, it is clear that the decontamination effect is proportionally dependent on the concentration (5c at concentration of 0.1%, 0.05% and 0.01% causes the elimination of 80.47 ± 4.61%, 58.16 ± 7.23% and 29.04 ± 8.80% of bacteria, respectively) ( Figure 5).

Antibiofilm Activity and Comparison in Effectiveness against S. aureus in Planktonic and Biofilm Form
To evaluate the efficacy of the novel series against the biofilm form, which is much more resistant than the planktonic form and can often cause a relapse of the infection, a S. aureus biofilm formed on a polystyrene surface for 24 h was exposed for 24 h to the 5b, 5c, 5d and BAC derivatives with C12, C14 and C16 alkyl chains. The minimal biofilm eradication concentration (MBEC) showed comparable activity between both tested series, and notably the MBECs values of 5b-d derivatives were slightly lower than the values for the corresponding BAC derivatives. Comparison of established MBEC and MBC values have shown that S. aureus in biofilm form was 4-64 times less susceptible to the tested compounds than in planktonic form. All results are depicted in Figure 6.

Virucidal Activity against Enveloped Viruses
To evaluate the width of the spectrum against different microorganisms, the virucidal activity of 5b-d on murine cytomegalovirus (MCMV) and SARS-CoV-2 virus was determined using a quantitative suspension assay. Virus titer was evaluated using the Spearman-Karber method and expressed as logTCID50/mL [32]. In accordance with EN 14476 for disinfection with full virucidal activity, the substance should demonstrate a reduction in virus titer of at least 4 orders of magnitude, corresponding to 99.99% inactivation [33]. The morphological changes of one layer of cells were monitored to distinguish between the virus-induced cytopathic changes and the toxic effect caused by the test substance. The highest efficiency was shown by substance 5b, where the virus titer decreased by more than 5 orders of magnitude at a concentration of 0.01% (Table 4). The decrease could not be determined exactly for the compounds at a concentration of 0.1% (marked>), as the tested substances at this concentration already affected the cell culture which was used for growing the virus. Evaluation against SARS-CoV-2 showed that 5b and 5c showed only a modest effect at a concentration of 0.01%. Unfortunately, at higher concentration (0.1%), growth of the cells for culturing the virus was affected and the effect reaching the required value of a decrease of 4 logarithms cannot be confirmed.

Cell Viability Evaluation and Selectivity Index
To define the cytotoxic selectivity, i.e., safety, towards eukaryotic cells, in vitro cytotoxicity studies were performed using the mammalian Chinese hamster ovary (CHO)-K1 cell line. The values of IC 50 (half maximal inhibitory concentration) confirmed the predicted trend of the correlation described earlier for the homolog group, i.e., elongation of the alkyl chain length increases the cytotoxic potential of the drugs (Table 5) [29,31]. This effect is related to the increasing lipophilicity expressed as the Clog P (Table 5), and most likely correlates with the easier ability to penetrate cells. Notably, considering the identical BAC homologs (BAC 12-16), we can conclude that the introduction of the hydroxyethyl groups into the structure increases the IC 50 value and therefore reduces the toxicity of the substances. Furthermore, the selectivity indexes were calculated as the ration of IC 50 /MIC (24 h) for all bacterial strains (Table 6).

Conclusions
The series of benzoxonium-like salts with alkyl chain length C 10 , C 12 , C 14 , C 16 and C 18 was identified as promising active ingredients for chemical-biological decontamination. Critical micellar concentration as a standard characteristic of surfactants has shown a suitable concentration for chemical decontamination and the efficacy in fenitrothion degradation surpassed that of all the reference compounds. Biocidal activity against various strains of bacteria including F. tularensis and S. aureus in biofilm form was also determined to discover biological decontamination potential. The homolog with a chain length of C 12 (5b) shows the highest biocidal activity. However, the best effect for chemical decontamination is observed for derivatives with a longer alkyl chain (i.e., compounds 5d, 5e). In addition, the compounds seem to be safe on mammalian cell lines as a basic safety parameter for potential use in practice. Finally, BOC-type compounds have been found to have a significant dual effect against both chemical and biological agents. It is thus possible to envisage their use, individually or in a mixture, as active components of multi-purpose decontamination products.