Prednisolone inhibits phagocytosis by polymorphonuclear leucocytes via steroid receptor mediated events

Prednisolone, at concentrations between 2·78 × 10⁻⁶ M (1 μg/ml) and 1·39 × 10⁻⁸ M (5 × 10⁻³ μg/ml) exerts an inhibitory effect on the phagocytosis of latex particles by normal human polymorphonuclear leucocytes in vitro as assessed by electron microscopical analysis. This inhibition appears to be receptor-mediated, as it is dependent upon RNA and protein synthesis and is glucocorticoid specific.     

Mechanical Behavior of Titanium Based Metal Matrix Composites Reinforced with TiC or TiB Particles under Quasi-Static and High Strain-Rate Compression

The mechanical behavior of titanium alloys has been mostly studied in quasi-static conditions when the strain rate does not exceed 10 s⁻¹, while the studies performed in dynamic settings specifically for Ti-based composites are limited. Such data are critical to prevent the “strength margin” approach, which is used to assure the part performance under dynamic conditions in the absence of relevant data. The purpose of this study was to obtain data on the mechanical behavior of Ti-based composites under dynamic condition. The Metal Matrix Composites (MMC) on the base of the alloy Ti-6Al-4V (wt.%) were made using Blended Elemental Powder Metallurgy with different amounts of reinforcing particles: 5, 10, and 20% of TiC or 5, 10% (vol.) of TiB. Composites were studied at high strain rate compression ~1–3·10³·s⁻¹ using the split Hopkinson pressure bar. Mechanical behavior was analyzed considering strain rate, phase composition, microstructure, and strain energy (SE). It is shown that for the strain rates up to 1920 s⁻¹, the strength and SE of MMC with 5% TiC are substantially higher compared to particles free alloy. The particles TiC localize the plastic deformation at the micro level, and fracturing occurs mainly by crushing particles and their aggregates. TiB MMCs have a finer grain structure and different mechanical behavior. MMC with 5 and 10% TiB do not break down at strain rates up to almost 3000 s⁻¹; and 10% MMC surpasses other materials in the SE at strain rates exceeding 2200 s⁻¹. The deformation mechanism of MMCs was evaluated.     

Microstructure Evolution,Constitutive Modelling,and Superplastic Forming of Experimental 6XXX-Type Alloys Processed with Different Thermomechanical Treatments

This study focused on the microstructural analysis, superplasticity, modeling of superplastic deformation behavior, and superplastic forming tests of the Al-Mg-Si-Cu-based alloy modified with Fe, Ni, Sc, and Zr. The effect of the thermomechanical treatment with various proportions of hot/cold rolling degrees on the secondary particle distribution and deformation behavior was studied. The increase in hot rolling degree increased the homogeneity of the particle distribution in the aluminum-based solid solution that improved superplastic properties, providing an elongation of ~470–500% at increased strain rates of (0.5–1) × 10⁻² s⁻¹. A constitutive model based on Arrhenius and Beckofen equations was used to describe and predict the superplastic flow behavior of the alloy studied. Model complex-shaped parts were processed by superplastic forming at two strain rates. The proposed strain rate of 1 × 10⁻² s⁻¹ provided a low thickness variation and a high quality of the experimental parts. The residual cavitation after superplastic forming was also large at the low strain rate of 2 × 10⁻³ s⁻¹ and significantly smaller at 1 × 10⁻² s⁻¹. Coarse Al₉FeNi particles did not stimulate the cavitation process and were effective to provide the superplasticity of alloys studied at high strain rates, whereas cavities were predominately observed near coarse Mg₂Si particles, which act as nucleation places for cavities during superplastic deformation and forming.     

A High-Strain-Rate Superplasticity of the Al-Mg-Si-Zr-Sc Alloy with Ni Addition

The current study analyzed the effect of Ni content on the microstructure and superplastic deformation behavior of the Al-Mg-Si-Cu-based alloy doped with small additions of Sc and Zr. The superplasticity was observed in the studied alloys due to a bimodal particle size distribution. The coarse particles of eutectic origin Al₃Ni and Mg₂Si phases with a total volume fraction of 4.0–8.0% and a mean size of 1.4–1.6 µm provided the particles with a stimulated nucleation effect. The L1₂– structured nanoscale dispersoids of Sc- and Zr-bearing phase inhibited recrystallization and grain growth due to a strong Zener pinning effect. The positive effect of Ni on the superplasticity was revealed and confirmed by a high-temperature tensile test in a wide strain rate and temperature limits. In the alloy with 4 wt.% Ni, the elongation-to-failure of 350–520% was observed at 460 °C, in a strain rate range of 2 × 10⁻³–5 × 10⁻² s⁻¹.     

An Analytical Model for Estimating the Bending Curvatures of Metal Sheets in Laser Peen Forming

Laser peen forming (LPF) is suitable for shaping sheet metals without the requirement for die/mold and without causing high temperatures. An analytical model for estimating the bending curvatures of LPF is convenient and necessary for better understanding of the physical processes involved. In this paper, we describe a new analytical model based on internal force balance and the energy transformation in LPF. Experiments on 2024 aluminum alloy sheets of 1–3 mm thickness were performed to validate the analytical model. The results showed that for 1 mm and 3 mm thick–thin plates, the curvature obtained by the analytical model changes from −14 × 10⁻⁴ mm⁻¹ and −1 × 10⁻⁴ mm⁻¹ to 55 × 10⁻⁴ mm⁻¹ and −21 × 10⁻⁴ mm⁻¹, respectively, with the increase of laser energy, which is consistent with the experimental trend. So, when either the stress gradient mechanism (SGM) or the shock bending mechanism (SBM) overwhelmingly dominated the forming process, the analytical model could give relatively accurate predicted curvatures compared with the experimental data. Under those conditions where SGM and SBM were comparable, the accuracy of the model was low, because of the complex stress distributions within the material, and the complex energy coupling process under these conditions.     

Importance of trivalency and the eg1 configuration in the photocatalytic oxidation of water by Mn and Co oxides

Prompted by the early results on the catalytic activity of LiMn₂O₄ and related oxides in the photochemical oxidation of water, our detailed study of several manganese oxides has shown that trivalency of Mn is an important factor in determining the catalytic activity. Thus, Mn₂O₃, LaMnO₃, and MgMn₂O₄ are found to be very good catalysts with turnover frequencies of 5 × 10⁻⁴ s⁻¹, 4.8 × 10⁻⁴ s⁻¹, and 0.8 ×10⁻⁴ s⁻¹, respectively. Among the cobalt oxides, Li₂Co₂O₄ and LaCoO₃—especially the latter—exhibit excellent catalytic activity, with the turnover frequencies being 9 × 10⁻⁴ s⁻¹ and 1.4 × 10⁻³ s⁻¹, respectively. The common feature among the catalytic Mn and Co oxides is not only that Mn and Co are in the trivalent state, but Co³⁺ in the Co oxides is in the intermediate t_2g⁵e_g¹ state whereas Mn³⁺ is in the t_2g³e_g¹ state. The presence of the e_g¹ electron in these Mn and Co oxides is considered to play a crucial role in the photocatalytic properties of the oxides.     

Adjustment for the influence of age and heart rate on Doppler measurements of left ventricular filling

Objective—To determine the normal range of pulsed Doppler measurements of left ventricular filling adjusted for age and heart rate.

Design—Multiple regression was used to measure the effects of age and heart rate on pulsed Doppler indices of left ventricular filling in normal subjects. These regression equations were used to calculate a predicted normal value and 95% confidence interval (95% CI) for any subject from his age and heart rate.

Participants—61 subjects with no evidence of cardiovascular disease, aged 20 to 90 years, with a resting heart rate of 47–89 beats/min.

Results—The effect of a 10 year increase in age was peak atrial filling velocity +15% (95% CI 12·0% to 18·5%); peak early filling velocity −3·2% (−6·0% to 0%); isovolumic relaxation time +6·2% (3·9% to 8·4%); acceleration time −3·8% (−6·0% to −1·5%); deceleration time +7·9% (5·1% to 10·8%). The effect of a 10 beat/min increase in heart rate was: peak atrial filling velocity +5·5% (1·2% to 10·1%); peak early filling velocity −4·0% (−8·1% to 2·0%); isovolumic relaxation time −2·5% (−4·6% to 0·6%); acceleration time −3·1% (−6·4% to 0·4%); decleration time −1·8% (−4·0% to 3·8%).

Conclusion—For any individual, comparison of the predicted normal measurement and 95% CI with the observed measurement allows an assessment of the effects of disease on left ventricular filling that is independent of age and heart rate.

     

Electrochemically Activated Screen-Printed Carbon Sensor Modified with Anionic Surfactant (aSPCE/SDS) for Simultaneous Determination of Paracetamol,Diclofenac and Tramadol

In this work, an electrochemically activated screen-printed carbon electrode modified with sodium dodecyl sulfate (aSPCE/SDS) was proposed for the simultaneous determination of paracetamol (PA), diclofenac (DF), and tramadol (TR). Changes of surface morphology and electrochemical behaviour of the electrode after the electrochemical activation with H₂O₂ and SDS surface modification were studied by scanning electron microscopy (SEM), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). The influence of various parameters on the responses of the aSPCE/SDS such as pH and concentration of the buffer, SDS concentration, and techniques parameters were investigated. Using optimised conditions (E_acc. of −0.4 V, t_acc. of 120 s, ΔE_A of 150 mV, ν of 250 mV s⁻¹, and t_m of 10 ms), the aSPCE/SDS showed a good linear response in the concentration ranges of 5.0 × 10⁻⁸–2.0 × 10⁻⁵ for PA, 1.0 × 10⁻⁹–2.0 × 10⁻⁷ for DF, and 1.0 × 10⁻⁸–2.0 × 10⁻⁷ and 2.0 × 10⁻⁷–2.0 × 10⁻⁶ mol L⁻¹ for TR. The limits of detection obtained during the simultaneous determination of PA, DF, and TR are 1.49 × 10⁻⁸ mol L⁻¹, 2.10 × 10⁻¹⁰ mol L⁻¹, and 1.71 × 10⁻⁹ mol L⁻¹, respectively. The selectivity of the aSPCE/SDS was evaluated by examination of the impact of some inorganic and organic substances that are commonly present in environmental and biological samples on the responses of PA, DF, and TR. Finally, the differential pulse adsorptive stripping voltammetric (DPAdSV) procedure using the aSPCE/SDS was successfully applied for the determination of PA, DF, and TR in river water and serum samples as well as pharmaceuticals.     

Adjustment for the influence of age and heart rate on Doppler measurements of left ventricular filling

Objective—To determine the normal range of pulsed Doppler measurements of left ventricular filling adjusted for age and heart rate.Design—Multiple regression was used to measure the effects of age and heart rate on pulsed Doppler indices of left ventricular filling in normal subjects. These regression equations were used to calculate a predicted normal value and 95% confidence interval (95% CI) for any subject from his age and heart rate.Participants—61 subjects with no evidence of cardiovascular disease, aged 20 to 90 years, with a resting heart rate of 47–89 beats/min.Results—The effect of a 10 year increase in age was peak atrial filling velocity +15% (95% CI 12·0% to 18·5%); peak early filling velocity −3·2% (−6·0% to 0%); isovolumic relaxation time +6·2% (3·9% to 8·4%); acceleration time −3·8% (−6·0% to −1·5%); deceleration time +7·9% (5·1% to 10·8%). The effect of a 10 beat/min increase in heart rate was: peak atrial filling velocity +5·5% (1·2% to 10·1%); peak early filling velocity −4·0% (−8·1% to 2·0%); isovolumic relaxation time −2·5% (−4·6% to 0·6%); acceleration time −3·1% (−6·4% to 0·4%); decleration time −1·8% (−4·0% to 3·8%).Conclusion—For any individual, comparison of the predicted normal measurement and 95% CI with the observed measurement allows an assessment of the effects of disease on left ventricular filling that is independent of age and heart rate.     

Fickian-Based Empirical Approach for Diffusivity Determination in Hollow Alginate-Based Microfibers Using 2D Fluorescence Microscopy and Comparison with Theoretical Predictions

Hollow alginate microfibers (od = 1.3 mm, id = 0.9 mm, th = 400 µm, L = 3.5 cm) comprised of 2% (w/v) medium molecular weight alginate cross-linked with 0.9 M CaCl₂ were fabricated to model outward diffusion capture by 2D fluorescent microscopy. A two-fold comparison of diffusivity determination based on real-time diffusion of Fluorescein isothiocyanate molecular weight (FITC MW) markers was conducted using a proposed Fickian-based approach in conjunction with a previously established numerical model developed based on spectrophotometric data. Computed empirical/numerical (D_empiricial/D_numerical) diffusivities characterized by small standard deviations for the 4-, 70- and 500-kDa markers expressed in m²/s are (1.06 × 10⁻⁹ ± 1.96 × 10⁻¹⁰)/(2.03 × 10⁻¹¹), (5.89 × 10⁻¹¹ ± 2.83 × 10⁻¹²)/(4.6 × 10⁻¹²) and (4.89 × 10⁻¹² ± 3.94 × 10⁻¹³)/(1.27 × 10⁻¹²), respectively, with the discrimination between the computation techniques narrowing down as a function of MW. The use of the numerical approach is recommended for fluorescence-based measurements as the standard computational method for effective diffusivity determination until capture rates (minimum 12 fps for the 4-kDa marker) and the use of linear instead of polynomial interpolating functions to model temporal intensity gradients have been proven to minimize the extent of systematic errors associated with the proposed empirical method.     

Kinetics of the Organic Compounds and Ammonium Nitrogen Electrochemical Oxidation in Landfill Leachates at Boron-Doped Diamond Anodes

Electrochemical oxidation (EO) of organic compounds and ammonium in the complex matrix of landfill leachates (LLs) was investigated using three different boron-doped diamond electrodes produced on silicon substrate (BDD/Si)(levels of boron doping [B]/[C] = 500, 10,000, and 15,000 ppm—0.5 k; 10 k, and 15 k, respectively) during 8-h tests. The LLs were collected from an old landfill in the Pomerania region (Northern Poland) and were characterized by a high concentration of N-NH₄⁺ (2069 ± 103 mg·L⁻¹), chemical oxygen demand (COD) (3608 ± 123 mg·L⁻¹), high salinity (2690 ± 70 mg Cl⁻·L⁻¹, 1353 ± 70 mg SO₄²⁻·L⁻¹), and poor biodegradability. The experiments revealed that electrochemical oxidation of LLs using BDD 0.5 k and current density (j) = 100 mA·cm⁻² was the most effective amongst those tested (C_8h/C₀: COD = 0.09 ± 0.14 mg·L⁻¹, N-NH₄⁺ = 0.39 ± 0.05 mg·L⁻¹). COD removal fits the model of pseudo-first-order reactions and N-NH₄⁺ removal in most cases follows second-order kinetics. The double increase in biodegradability index—to 0.22 ± 0.05 (BDD 0.5 k, j = 50 mA·cm⁻²) shows the potential application of EO prior biological treatment. Despite EO still being an energy consuming process, optimum conditions (COD removal > 70%) might be achieved after 4 h of treatment with an energy consumption of 200 kW·m⁻³ (BDD 0.5 k, j = 100 mA·cm⁻²).     

Preparation and Properties of Electrodeposited Ni-B-Graphene Oxide Composite Coatings

With the rapid development of modern industries, the surface quality and performance of metals need to be improved. Composite electrodeposition (co-deposition) has evolved as an important technique for improving the surface performance of metal materials. Herein, a new type of graphene oxide (GO)-reinforced nickel–boron (Ni-B) composite coating was successfully prepared on a 7075 aluminum (Al) alloy by co-deposition. Characterization revealed a significant improvement in the mechanical and anti-corrosion properties of the composite with the incorporation of GOs. The composite showed a rougher, compact, cauliflower-like morphology with finer grains, a higher hardness (1532 HV), a lower rate of wear (5.20 × 10⁻⁵ mm³∙N⁻¹∙m⁻¹), and a lower corrosion rate (33.66 × 10⁻³ mm∙y⁻¹) compared with the Ni-B alloy deposit (878 HV, 9.64 × 10⁻⁵ mm³∙N⁻¹∙m⁻¹, and 116.64 × 10⁻³ mm∙y⁻¹, respectively). The mechanism by which GOs strengthen the Ni-B matrix is discussed.     

Rapid Detection of Listeria by Bacteriophage Amplification and SERS-Lateral Flow Immunochromatography

A rapid Listeria detection method was developed utilizing A511 bacteriophage amplification combined with surface-enhanced Raman spectroscopy (SERS) and lateral flow immunochromatography (LFI). Anti-A511 antibodies were covalently linked to SERS nanoparticles and printed onto nitrocellulose membranes. Antibody-conjugated SERS nanoparticles were used as quantifiable reporters. In the presence of A511, phage-SERS nanoparticle complexes were arrested and concentrated as a visible test line, which was interrogated quantitatively by Raman spectroscopy. An increase in SERS intensity correlated to an increase in captured phage-reporter complexes. SERS limit of detection was 6 × 10⁶ pfu·mL⁻¹, offering detection below that obtainable by the naked eye (LOD 6 × 10⁷ pfu·mL⁻¹). Phage amplification experiments were carried out at a multiplicity of infection (MOI) of 0.1 with 4 different starting phage concentrations monitored over time using SERS-LFI and validated by spot titer assay. Detection of L. monocytogenes concentrations of 1 × 10⁷ colony forming units (cfu)·mL⁻¹, 5 × 10⁶ cfu·mL⁻¹, 5 × 10⁵ cfu·mL⁻¹ and 5 × 10⁴ cfu·mL⁻¹ was achieved in 2, 2, 6, and 8 h, respectively. Similar experiments were conducted at a constant starting phage concentration (5 × 10⁵ pfu·mL⁻¹) with MOIs of 1, 2.5, and 5 and were detected in 2, 4, and 5 h, respectively.     

Solubilization and Thermodynamic Analysis of Isotretinoin in Eleven Different Green Solvents at Different Temperatures

The solubilization and thermodynamic analysis of isotretinoin (ITN) in eleven distinct green solvents, such as water, methyl alcohol (MeOH), ethyl alcohol (EtOH), 1-butyl alcohol (1-BuOH), 2-butyl alcohol (2-BuOH), ethane-1,2-diol (EG), propane-1,2-diol (PG), polyethylene glycol-400 (PEG-400), ethyl acetate (EA), Transcutol-HP (THP), and dimethyl sulfoxide (DMSO) was studied at several temperatures and a fixed atmospheric pressure. The equilibrium approach was used to measure the solubility of ITN, and the Apelblat, van’t Hoff, and Buchowski–Ksiazczak λh models were used to correlate the results. The overall uncertainties were less than 5.0% for all the models examined. The highest ITN mole fraction solubility was achieved as 1.01 × 10⁻¹ in DMSO at 318.2 K; however, the least was achieved as 3.16 × 10⁻⁷ in water at 298.2 K. ITN solubility was found to be enhanced with an increase in temperature and the order in which it was soluble in several green solvents at 318.2 K was as follows: DMSO (1.01 × 10⁻¹) > EA (1.73 × 10⁻²) > PEG-400 (1.66 × 10⁻²) > THP (1.59 × 10⁻²) > 2-BuOH (6.32 × 10⁻³) > 1-BuOH (5.88 × 10⁻³) > PG (4.83 × 10⁻³) > EtOH (3.51 × 10⁻³) > EG (3.49 × 10⁻³) > MeOH (2.10 × 10⁻³) > water (1.38 × 10⁻⁶). ITN–DMSO showed the strongest solute–solvent interactions when compared to the other ITN and green solvent combinations. According to thermodynamic studies, ITN dissolution was endothermic and entropy-driven in all of the green solvents tested. The obtained outcomes suggested that DMSO appears to be the best green solvent for ITN solubilization.     

Influence of Different Thermal Aging Conditions on Soot Combustion with Catalyst by Thermogravimetric Analysis

Diesel particulates are deposited in the diesel particulate filter and removed by the regeneration process. The Printex-U (PU) particles are simulated as the diesel soot to investigate the influence of thermal aging conditions on soot combustion performance with the addition of catalysts. The comprehensive combustion index S, combustion stability index R_w and peak temperature T_p are obtained to evaluate the combustion performance. Compared with the PU/Pt mixtures of different Pt contents (2 g/ft³, 3.5 g/ft³, and 5 g/ft³), the 10 g/ft³ Pt contents improve soot combustion with the outstanding oxygen absorption ability. When the weight ratio of PU/Pt mixture is 1:1, the promoted effect achieves the maximum degree. The S and R_w increase to 8.90 × 10⁻⁸ %²min⁻²°C⁻³ and 39.11 × 10⁵, respectively, compared with pure PU. After the thermal aging process, the PU/Pt mixture with a 350 °C aging temperature for 10 h promotes the soot combustion the best when compared to pure PU particles. It is not good as the PU/Pt mixture without aging, because the inner properties of soot and Pt/Al₂O₃ catalyst may have been changed. The S and R_w are 9.07 × 10⁻⁸ %²min⁻²°C⁻³ and 38.39 × 10⁵, respectively, which are close to the no aging mixture. This work plays a crucial role in understanding the mechanism of the comprehensive effect of soot and catalyst on soot combustion after the thermal aging process.     

Degradation of Tetracycline with BiFeO3 Prepared by a Simple Hydrothermal Method

BiFeO₃ particles (BFO) were prepared by a simple hydrothermal method and characterized. BFO was pure, with a wide particle size distribution, and was visible light responsive. Tetracycline was chosen as the model pollutant in this study. The pH value was an important factor influencing the degradation efficiency. The total organic carbon (TOC) measurement was emphasized as a potential standard to evaluate the visible light photocatalytic degradation efficiency. The photo-Fenton process showed much better degradation efficiency and a wider pH adaptive range than photocatalysis or the Fenton process solely. The optimal residual TOC concentrations of the photocatalysis, Fenton and photo-Fenton processes were 81%, 65% and 21%, while the rate constants of the three processes under the same condition where the best residual TOC was acquired were 9.7 × 10⁻³, 3.2 × 10⁻² and 1.5 × 10⁻¹ min⁻¹, respectively. BFO was demonstrated to have excellent stability and reusability. A comparison among different reported advanced oxidation processes removing tetracycline (TC) was also made. Our findings showed that the photo-Fenton process had good potential for antibiotic-containing waste water treatment. It provides a new method to deal with antibiotic pollution.     

Electrochemically Pretreated Sensor Based on Screen-Printed Carbon Modified with Pb Nanoparticles for Determination of Testosterone

Testosterone (TST), despite its good properties, may be harmful to the human organism and the environment. Therefore, monitoring biological fluids and environmental samples is important. An electrochemically pretreated screen-printed carbon sensor modified with Pb nanoparticles (pSPCE/PbNPs) was successfully prepared and used for the determination of TST. The surface morphology and electrochemical properties of unmodified and modified sensors were characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), scanning and transmission electron microscopy (SEM and TEM), and energy-dispersive X-ray spectroscopy (EDS). Selective determinations of TST at the pSPCE/PbNPs were carried out by differential pulse adsorptive stripping voltammetry (DPAdSV, E_{Pb dep.and TST acc.} of −1.1 V, t _{Pb dep.and TST acc.} of 120 s, ΔE_A of 50 mV, ν of 175 mV s⁻¹, and t_m of 5 ms) in a solution containing 0.075 mol L⁻¹ acetate buffer of pH = 4.6 ± 0.1, and 7.5 × 10⁻⁵ mol L⁻¹ Pb(NO₃)₂. The analytical signal obtained at the potential around −1.42 V (vs. silver pseudo-reference electrode) is related to the reduction process of TST adsorbed onto the electrode surface. The use of pSPCE/PbNPs allows obtaining a very low limit of TST detection (2.2 × 10⁻¹² mol L⁻¹) and wide linear ranges of the calibration graph (1.0 × 10⁻¹¹–1.0 × 10⁻¹⁰, 1.0 × 10⁻¹⁰–2.0 × 10⁻⁹, and 2.0 × 10⁻⁹–2.0 × 10⁻⁸ mol L⁻¹). The pSPCE/PbNPs were successfully applied for the determination of TST in reference material of human urine and wastewater purified in a sewage treatment plant without preliminary preparation.     

Characterisation of Particle Size and Viability of SARS-CoV-2 Aerosols from a Range of Nebuliser Types Using a Novel Sampling Technique

Little is understood about the impact of nebulisation on the viability of SARS-CoV-2. In this study, a range of nebulisers with differing methods of aerosol generation were evaluated to determine SARS-CoV-2 viability following aerosolization. The aerosol particle size distribution was assessed using an aerosol particle sizer (APS) and SARS-CoV-2 viability was determined after collection into liquid media using All-Glass Impingers (AGI). Viable particles of SARS-CoV-2 were further characterised using the Collison 6-jet nebuliser in conjunction with novel sample techniques in an Andersen size-fractioning sampler to predict lung deposition profiles. Results demonstrate that all the tested nebulisers can generate stable, polydisperse aerosols (Geometric standard deviation (GSD) circa 1.8) in the respirable range (1.2 to 2.2 µm). Viable fractions (VF, units PFU/particle, the virus viability as a function of total particles produced) were circa 5 × 10⁻³. VF and spray factors were not significantly affected by relative humidity, within this system where aerosols were in the spray tube an extremely short time. The novel Andersen sample collection methods successfully captured viable virus particles across all sizes; with most particle sizes below 3.3 µm. Particle sizes, in MMAD (Mass Median Aerodynamic Diameters), were calculated from linear regression of log₁₀-log₁₀ transformed cumulative PFU data, and calculated MMADs accorded well with APS measurements and did not differ across collection method types. These data will be vital in informing animal aerosol challenge models, and infection prevention and control policies.     

Copper Film Modified Glassy Carbon Electrode and Copper Film with Carbon Nanotubes Modified Screen-Printed Electrode for the Cd(II) Determination

A copper film modified glassy carbon electrode (CuF/GCE) and a novel copper film with carbon nanotubes modified screen-printed electrode (CuF/CN/SPE) for anodic stripping voltammetric measurement of ultratrace levels of Cd(II) are presented. During the development of the research procedure, several main parameters were investigated and optimized. The optimal electroanalytical performance of the working electrodes was achieved in electrolyte 0.1 M HCl and 2 × 10⁻⁴ M Cu(II). The copper film modified glassy carbon electrode exhibited operation in the presence of dissolved oxygen with a calculated limit of detection of 1.7 × 10⁻¹⁰ M and 210 s accumulation time, repeatability with RSD of 4.2% (n = 5). In the case of copper film with carbon nanotubes modified screen-printed electrode limit of detection amounted 1.3 × 10⁻¹⁰ M for accumulation time of 210 s and with RSD of 4.5% (n = 5). The calibration curve has a linear range in the tested concentration of 5 × 10⁻¹⁰–5 × 10⁻⁷ M (r = 0.999) for CuF/GCE and 3 × 10⁻¹⁰–3 × 10⁻⁷ M (r = 0.999) for CuF/CN/SPE with 210 s accumulation time in both cases. The used electrodes enable trace determination of cadmium in different environmental water samples containing organic matrix. The validation of the proposed procedures was carried out through analysis certified reference materials: TM-25.5, SPS-SW1, and SPS-WW1.