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Managing tibial fractures requires substantial health resources, which costs the health system. This study aimed to describe the costs of photobiomodulation (PBM) with LEDs in the healing process of soft tissue lesions associated with tibial fracture compared to a placebo. Economic analysis was performed based on a randomized controlled clinical trial, with a simulation of the cost-effectiveness and incremental cost model. Adults (n = 27) hospitalized with tibia fracture awaiting definitive surgery were randomized into two distinct groups: the PBM Group (n = 13) and the Control Group with simulated phototherapy (n = 14). To simulate the cost-effectiveness and incremental cost model, the outcome was the evolution of wound resolution by the BATES-JENSEN scale and time of wound resolution in days. The total cost of treatment for the Control group was R$21,164.56, and a difference of R$7,527.10 more was observed when compared to the treatment of the PBM group. The proposed intervention did not present incremental cost since the difference in the costs to reduce measures between the groups was smaller for the PBM group. When analyzing the ICER (Incremental cost-effectiveness ratio), it would be possible to save R$3,500.98 with PBM and decrease by 2.15 points in the daily average on the BATES-JENSEN scale. It is concluded, therefore, that PBM can be a supportive therapy of clinical and economic interest in a hospital setting. [ABSTRACT FROM AUTHOR]

Decomposition kinetics of stabilised CH2OO and CD2OO Criegee intermediates have been investigated as a function of temperature (450–650 K) and pressure (2–350 Torr) using flash photolysis coupled with time-resolved cavity-enhanced broadband UV absorption spectroscopy. Decomposition of CD2OO was observed to be faster than CH2OO under equivalent conditions. Production of OH radicals following CH2OO decomposition was also monitored using flash photolysis with laser-induced fluorescence (LIF), with results indicating direct production of OH in the v = 0 and v = 1 states in low yields. Master equation calculations performed using the Master Equation Solver for Multi-Energy well Reactions (MESMER) enabled fitting of the barriers for the decomposition of CH2OO and CD2OO to the experimental data. Parameterisations of the decomposition rate coefficients, calculated by MESMER, are provided for use in atmospheric models and implications of the results are discussed. For CH2OO, the MESMER fits require an increase in the calculated barrier height from 78.2 kJ mol−1 to 81.8 kJ mol−1 using a temperature-dependent exponential down model for collisional energy transfer with 〈ΔE〉down = 32.6(T/298 K)1.7 cm−1 in He. The low- and high-pressure limit rate coefficients are k1,0 = 3.2 × 10−4(T/298)−5.81exp(−12 770/T) cm3 s−1 and k1,∞ = 1.4 × 1013(T/298)0.06exp(−10 010/T) s−1, with median uncertainty of ∼12% over the range of experimental conditions used here. Extrapolation to atmospheric conditions yields k1(298 K, 760 Torr) = 1.1+1.5−1.1× 10−3 s−1. For CD2OO, MESMER calculations result in 〈ΔE〉down = 39.6(T/298 K)1.3 cm−1 in He and a small decrease in the calculated barrier to decomposition from 81.0 kJ mol−1 to 80.1 kJ mol−1. The fitted rate coefficients for CD2OO are k2,0 = 5.2 × 10−5(T/298)−5.28exp(−11 610/T) cm3 s−1 and k2,∞ = 1.2 × 1013(T/298)0.06exp(−9800/T) s−1, with overall error of ∼6% over the present range of temperature and pressure. The extrapolated k2(298 K, 760 Torr) = 5.5+9.2−5.5× 10−3 s−1. The master equation calculations for CH2OO indicate decomposition yields of 63.7% for H2 + CO2, 36.0% for H2O + CO and 0.3% for OH + HCO with no significant dependence on temperature between 400 and 1200 K or pressure between 1 and 3000 Torr. [ABSTRACT FROM AUTHOR]

Abstract: The rate coefficients of the reactions of OH radicals and Cl atoms with three alkylcyclohexanes compounds, methylcyclohexane (MCH), trans‐1,4‐dimethylcyclohexane (DCH), and ethylcyclohexane (ECH) have been investigated at (293 ± 1) K and 1000 mbar of air using relative rate methods. A majority of the experiments were performed in the Highly Instrumented Reactor for Atmospheric Chemistry (HIRAC), a stainless steel chamber using in situ FTIR analysis and online gas chromatography with flame ionization detection (GC‐FID) detection to monitor the decay of the alkylcyclohexanes and the reference compounds. The studies were undertaken to provide kinetic data for calibrations of radical detection techniques in HIRAC. The following rate coefficients (in cm3 molecule−1 s−1) were obtained for Cl reactions: k(Cl+MCH) = (3.51 ± 0.37) × 10–10, k(Cl+DCH) = (3.63 ± 0.38) × 10−10, k(Cl+ECH) = (3.88 ± 0.41) × 10−10, and for the reactions with OH radicals: k(OH+MCH) = (9.5 ± 1.3) × 10–12, k(OH+DCH) = (12.1 ± 2.2) × 10−12, k(OH+ECH) = (11.8 ± 2.0) × 10−12. Errors are a combination of statistical errors in the relative rate ratio (2σ) and the error in the reference rate coefficient. Checks for possible systematic errors were made by the use of two reference compounds, two different measurement techniques, and also three different sources of OH were employed in this study: photolysis of CH3ONO with black lamps, photolysis of H2O2 at 254 nm, and nonphotolytic trans‐2‐butene ozonolysis. For DCH, some direct laser flash photolysis studies were also undertaken, producing results in good agreement with the relative rate measurements. Additionally, temperature‐dependent rate coefficient investigations were performed for the reaction of methylcyclohexane with the OH radical over the range 273‐343 K using the relative rate method; the resulting recommended Arrhenius expression is k(OH + MCH) = (1.85 ± 0.27) × 10–11 exp((–1.62 ± 0.16) kJ mol−1/RT) cm3 molecule−1 s−1. The kinetic data are discussed in terms of OH and Cl reactivity trends, and comparisons are made with the existing literature values and with rate coefficients from structure‐activity relationship methods. This is the first study on the rate coefficient determination of the reaction of ECH with OH radicals and chlorine atoms, respectively. [ABSTRACT FROM AUTHOR]

Fast radical reactions are central to the chemistry of planetary atmospheres and combustion systems. Laser-induced fluorescence is a highly sensitive and selective technique that can be used to monitor a number of radical species in kinetics experiments, but is typically limited to low pressure systems owing to quenching of fluorescent states at higher pressures. The design and characterisation of an instrument are reported using laser-induced fluorescence detection to monitor fast radical kinetics (up to 25 000 s-1) at high temperatures and pressures by sampling from a high pressure reaction region to a low pressure detection region. Kinetics have been characterised at temperatures reaching 740 K and pressures up to 2 atm, with expected maximum operational conditions of up to ~900 K and ~5 atm. The distance between the point of sampling from the high pressure region and the point of probing within the low pressure region is critical to the measurement of fast kinetics. The instrumentation described in this work can be applied to the measurement of kinetics relevant to atmospheric and combustion chemistry. [ABSTRACT FROM AUTHOR]

The suitable computation of accurate atomic charges for the GROMACS topology *.itp files of small molecules, generated in the PRODRG server, has been a tricky task nowadays because it does not calculate atomic charges using an ab initio method. Usually additional steps of structure optimization and charges calculation, followed by a tedious manual replacement of atomic charges in the *.itp file, are needed. In order to assist this task, we report here the ITP Adjuster 1.0, a utility program developed to perform the replacement of the PRODRG charges in the *.itp files of small molecules by ab initio charges. [ABSTRACT FROM AUTHOR]

Compounds similar to lapatinib and gefitinib have been investigated as potential inhibitors of the intracellular receptor tyrosine kinase (RTK) domain of the human epidermal receptor 2 (HER2), which is a promising molecular target to the drug design of new chemotherapies for breast, lung, ovarian and colorectal cancers. In this study, we have searched potential HER2 inhibitors used for treatment of other illnesses such as hepatitis, bacterial infections and sexual impotence screened in the DrugBank. The compounds selected were subjected to virtual screening docking in order to evaluate the main interactions between them and the RTK domain of HER2. The selected compounds were investigated by flexible docking, molecular dynamics studies and ΔG bind calculations. The results suggest that antrafenine, saprisartan, reserpine, irinotecan and udenafil are potential candidates to inhibit the RTK domain of HER2. [ABSTRACT FROM AUTHOR]

Isomerization of N2O4 and dimerization of NO2 in thin water films on surfaces are believed to be key steps in the hydrolysis of NO2, which generates HONO, a significant precursor to the OH free radical in lower atmosphere and high-energy materials. Born--Oppenheimer molecular dynamics simulations using the density functional theory are carried out for NO2(H2O)m, m ≤ 4, and N2O4(H2O), clusters, n ≤ 7, used to mimic the surface reaction, to investigate the mechanism around room temperature. The results are (i) the NO2 dimerization and N2O4 isomerization reactions occur via two possible pathways, the non-water-assisted and water-assisted mechanisms; (ii) the NO2 dimerization in the presence of water yields either ONONO2(H2O)m or NO3-NO+(H2O) m clusters, but it is also possible to form the HNO3(NO2-)(H3O+)(H2O)m-2 transition state to form HONO and HNO3, directly; (iii) the N2O4 isomerization yields the NO3-NO+(H2O), cluster, but it does not hydrolyze faster than the NO2+NO2 -(H2O). hydrolysis to directly form the HONO and HNO3. New insights for hydrolysis of oxides of nitrogen in and on thin water films on surfaces in the atmosphere are discussed. [ABSTRACT FROM AUTHOR]

Literature rate coefficients for the prototypical radical-radical reaction at 298 K vary by close to an order of magnitude; such variations challenge our understanding of fundamental reaction kinetics. We have studied the title reaction at room temperature via the use of laser flash photolysis to generate OH and HO 2 radicals, monitoring OH by laser-induced fluorescence using two different approaches, looking at the direct reaction and also the perturbation of the slow OH + H 2 O 2 reaction with radical concentration, and over a wide range of pressures. Both approaches give a consistent measurement of k 1,298K ∼1 × 10 -11 cm 3 molecule -1 s -1 , at the lowest limit of previous determinations. We observe, experimentally, for the first time, a significant enhancement in the rate coefficient in the presence of water, k 1,H 2 O, 298K = (2.17 ± 0.09) × 10 -28 cm 6 molecule -2 s -1 , where the error is statistical at the 1σ level. This result is consistent with previous theoretical calculations, and the effect goes some way to explaining some, but not all, of the variation in previous determinations of k 1,298K . Supporting master equation calculations, using calculated potential energy surfaces at the RCCSD(T)-F12b/CBS//RCCSD/aug-cc-pVTZ and UCCSD(T)/CBS//UCCSD/aug-cc-pVTZ levels, are in agreement with our experimental observations. However, realistic variations in barrier heights and transition state frequencies give a wide range of calculated rate coefficients showing that the current precision and accuracy of calculations are insufficient to resolve the experimental discrepancies. The lower value of k 1,298K is consistent with experimental observations of the rate coefficient of the related reaction, Cl + HO 2 → HCl + O 2 . The implications of these results in atmospheric models are discussed., Competing Interests: The authors declare no competing financial interest., (© 2023 The Authors. Published by American Chemical Society.)

2-Methyl-1,3-butadiene (isoprene), released from biogenic sources, accounts for approximately a third of hydrocarbon emissions and is mainly removed by hydroxyl radicals, OH, the primary initiator of atmospheric oxidation. In situ measurements in clean tropical forests (high isoprene and low NO x ) have measured OH concentrations up to an order of magnitude higher than model predictions, which impacts our understanding of global oxidation. In this study, direct, laser flash photolysis, laser-induced fluorescence measurements at elevated temperatures have observed OH recycling in the presence of isoprene and oxygen under conditions where interference from secondary or heterogeneous chemistry is minimal. Our results provide the first direct, time-resolved, experimental validation of the theory-based Leuven Isoprene Mechanism (LIM1), based on isomerization of isoprene-RO 2 radicals and OH regeneration, that partially accounts for model:measurement divergence in OH. While our data can be fit with only minor alterations in important LIM1 parameters, and the overall rate of product formation is similar to LIM1, there are differences with the recent experimental study by Teng et al . J. Am. Chem. Soc. 2017 , 139 , 5367-5377. In addition, our study indicates that the dihydroperoxide products are significantly enhanced over previous estimates. Dihydroperoxides are chemical and photochemical sources of OH, and the implications of enhanced hydroperoxide formation on the agreement between models and observations in tropical forests are examined., Competing Interests: The authors declare no competing financial interest., (© 2022 The Authors. Published by American Chemical Society.)

Emissions of amines and amides to the atmosphere are significant from both anthropogenic and natural sources, and amides can be formed as secondary pollutants. Relatively little kinetic data exist on overall rate coefficients with OH, the most important tropospheric oxidant, and even less on site-specific data which control the product distribution. Structure-activity relationships (SARs) can be used to estimate both quantities. Rate coefficients for the reaction of OH with t -butylamine ( k 1 ), N -methyl-1,3-propanediamine ( k 2 ), and N -methylformamide ( k 3 ) have been measured using laser flash photolysis coupled with laser-induced fluorescence. Proton-transfer-reaction mass spectrometry (PTR-MS) has been used to ensure the reliable introduction of these low-vapor pressure N-containing compounds and to give qualitative information on products. Supporting ab initio calculations are presented for the t -butylamine system. The following rate coefficients have been determined: k 1,298K = (1.66 ± 0.20) × 10 -11 cm 3 molecule -1 s -1 , k ( T ) 1 = 1.65 × 10 -11 ( T /300) -0.69 cm 3 molecule -1 s -1 , k 2,293K = (7.09 ± 0.22) × 10 -11 cm 3 molecule -1 s -1 , and k 3,298K = (1.03 ± 0.23) × 10 -11 cm 3 molecule -1 s -1 . For OH + t -butylamine, ab initio calculations predict that the fraction of N-H abstraction is 0.87. The dominance of this channel was qualitatively confirmed using end-product analysis. The reaction of OH with N -methyl-1,3-propanediamine also had a negative temperature dependence, but the reduction in the rate coefficient was complicated by reagent loss. The measured rate coefficient for reaction 3 is in good agreement with a recent relative rate study. The results of this work and the literature data are compared with the recent SAR estimates for the reaction of OH with reduced nitrogen compounds. Although the SARs reproduce the overall rate coefficients for reactions, site-specific agreement with this work and other literature studies is less strong.

Decomposition kinetics of stabilised CH2OO and CD2OO Criegee intermediates have been investigated as a function of temperature (450-650 K) and pressure (2-350 Torr) using flash photolysis coupled with time-resolved cavity-enhanced broadband UV absorption spectroscopy. Decomposition of CD2OO was observed to be faster than CH2OO under equivalent conditions. Production of OH radicals following CH2OO decomposition was also monitored using flash photolysis with laser-induced fluorescence (LIF), with results indicating direct production of OH in the v = 0 and v = 1 states in low yields. Master equation calculations performed using the Master Equation Solver for Multi-Energy well Reactions (MESMER) enabled fitting of the barriers for the decomposition of CH2OO and CD2OO to the experimental data. Parameterisations of the decomposition rate coefficients, calculated by MESMER, are provided for use in atmospheric models and implications of the results are discussed. For CH2OO, the MESMER fits require an increase in the calculated barrier height from 78.2 kJ mol-1 to 81.8 kJ mol-1 using a temperature-dependent exponential down model for collisional energy transfer with ΔEdown = 32.6(T/298 K)1.7 cm-1 in He. The low- and high-pressure limit rate coefficients are k1,0 = 3.2 × 10-4(T/298)-5.81exp(-12 770/T) cm3 s-1 and k1,∞ = 1.4 × 1013(T/298)0.06exp(-10 010/T) s-1, with median uncertainty of ∼12% over the range of experimental conditions used here. Extrapolation to atmospheric conditions yields k1(298 K, 760 Torr) = 1.1+1.5-1.1 × 10-3 s-1. For CD2OO, MESMER calculations result in ΔEdown = 39.6(T/298 K)1.3 cm-1 in He and a small decrease in the calculated barrier to decomposition from 81.0 kJ mol-1 to 80.1 kJ mol-1. The fitted rate coefficients for CD2OO are k2,0 = 5.2 × 10-5(T/298)-5.28exp(-11 610/T) cm3 s-1 and k2,∞ = 1.2 × 1013(T/298)0.06exp(-9800/T) s-1, with overall error of ∼6% over the present range of temperature and pressure. The extrapolated k2(298 K, 760 Torr) = 5.5+9.2-5.5 × 10-3 s-1. The master equation calculations for CH2OO indicate decomposition yields of 63.7% for H2 + CO2, 36.0% for H2O + CO and 0.3% for OH + HCO with no significant dependence on temperature between 400 and 1200 K or pressure between 1 and 3000 Torr.

Isomerization of N(2)O(4) and dimerization of NO(2) in thin water films on surfaces are believed to be key steps in the hydrolysis of NO(2), which generates HONO, a significant precursor to the OH free radical in lower atmosphere and high-energy materials. Born-Oppenheimer molecular dynamics simulations using the density functional theory are carried out for NO(2)(H(2)O)(m), m ≤ 4, and N(2)O(4)(H(2)O)(n) clusters, n ≤ 7, used to mimic the surface reaction, to investigate the mechanism around room temperature. The results are (i) the NO(2) dimerization and N(2)O(4) isomerization reactions occur via two possible pathways, the non-water-assisted and water-assisted mechanisms; (ii) the NO(2) dimerization in the presence of water yields either ONONO(2)(H(2)O)(m) or NO(3)(-)NO(+)(H(2)O)(m) clusters, but it is also possible to form the HNO(3)(NO(2)(-))(H(3)O(+))(H(2)O)(m-2) transition state to form HONO and HNO(3), directly; (iii) the N(2)O(4) isomerization yields the NO(3)(-)NO(+)(H(2)O)(n) cluster, but it does not hydrolyze faster than the NO(2)(+)NO(2)(-)(H(2)O)(n) hydrolysis to directly form the HONO and HNO(3). New insights for hydrolysis of oxides of nitrogen in and on thin water films on surfaces in the atmosphere are discussed.