Search

Potassium-containing feldspars provide a high potential for producing potash, a product with widespread use in agriculture. The present work assesses applying the anti-solvent crystallization method for the purification and recovery of high-purity muriate of potash (KCl) from feldspar leaching solutions. Initially, screening experiments were carried out on a synthetic leaching solution with the aim of analyzing the crystallization behavior of key components. Screening experiments were performed using five anti-solvents, namely methanol, ethanol, acetone, 2-propanol, and ethylene glycol. Acetone and 2-propanol were viable options for crystallization of potassium chloride. Then, the effects of anti-solvent ratio (O/A), time, and anti-solvent addition rate on potassium-chloride crystallization were further investigated using acetone and 2-propanol. A recovery of 83% of potassium was achieved when using acetone at the O/A of 5 with the addition rate of 10 mL/min, at room temperature with a hold time of 180 min. The optimum conditions for 2-propanol were determined to be similar, except for using a 5 mL/min addition rate for 79% recovery. The final muriate of potash products had a purity of over 99.9% using either of the anti-solvent. However, differences in morphology and crystal size of products were observed. Acetone-formed potash crystals were aggregates of cubic crystals with an average size of 3 microns, while 2-propanol-formed potash crystals were 20 microns in size as cubic particles with a hollow core. Despite having almost the same performance in potassium recovery, acetone was found to be a more feasible anti-solvent for potash recovery due to simpler downstream solvent recovery. [ABSTRACT FROM AUTHOR]

In this study, Pd@TiO2 nanostructure is formed by using TiO2 fibers obtained by the electrospinning method and chemical reduction method, and this nanostructure is used in C2, and C3 alcohol oxidation studies as an application. In addition, TiO2 is compared with the Pd catalyst to investigate the effect of TiO2. In the results obtained, peak current values of 193 and 66.7 mA cm−2 for ethanol oxidation and 127.38 and 36.18 mA cm−2 for 2‐propanol oxidation are observed for Pd@TiO2 and Pd catalysts, respectively. With the addition of TiO2 to the structure, the electrocatalytic activity of C2 and C3 alcohol oxidations increases 3–3.5 times and contributes to the onset potential at an earlier potential. It also shows higher durability and stability in long‐term tests. Moreover, the addition of TiO2 to the structure enhances the electrocatalytic activity and provides high current density and long‐term stability in alcohol oxidation. These results show that fibrous structures in combination with metals improve the effect of catalysts and exhibit high potential for their application in alcohol fuel cells. [ABSTRACT FROM AUTHOR]

Objectives: This study assessed the effect of chlorhexidine (CHX) and isopropyl alcohol (IA) on immediate and late pushout bond strength (PBS) of fiber posts to dentin. Materials and Methods: In this in vitro study, 54 single-canal premolars were endodontically treated, and randomly assigned to 3 groups (N=18) for root dentin conditioning with distilled water (control), 2% CHX, and 70% IA after post space preparation. Fiber posts were cemented with TheraCem self-adhesive cement, and each group was subdivided into two subgroups (N=9) for PBS measurement immediately after bonding, and after 5000 thermal cycles (5-55°C). The roots were then sectioned, and their PBS was measured. The mode of failure was evaluated under a stereomicroscope at x40 magnification. Data were analyzed by repeated measures ANOVA and Tukey's test (alpha=0.05). Results: The highest PBS was noted in the IA group (21.12 MPa) after 24 hours and the lowest PBS belonged to the control group after thermocycling (7.48 MPa). The immediate and post-thermocycling PBS were significantly lower in the control group than the CHX group (P<0.05). The PBS in both the control and CHX groups was lower than that in the IA group (P<0.001). Regardless of the type of detergent, a significant reduction in PBS was observed after thermocycling (P<0.003). The PBS significantly decreased from the cervical towards the apical region in all groups (P<0.001). Conclusion: According to the results, application of IA before the self-adhesive cement effectively improved the immediate and late PBS, and was significantly more effective than CHX. [ABSTRACT FROM AUTHOR]

In the midst of the COVID-19 pandemic, the increased risk of exposure to 1-propanol has led the United States Food and Drug Administration to issue a warning about toxicity of 1-propanol-contaminated brands of hand sanitizers. We report a mixed intoxication with 1-propanol and 2-propanol in a patient who unintentionally ingested approximately 300 mL of hospital topical antiseptic solution and who presented to the emergency department with nausea, vomiting, and decreased level of consciousness. The patient developed an anion gap metabolic acidosis without an osmolar gap, elevated serum lactate, and undetectable serum beta-hydroxybutyrate. One hour later, he developed chest pain and was found to have an ST-segment elevation myocardial infarction. The patient underwent urgent coronary  angiography and stenting of the totally occluded mid-segment of the Left Anterior Descending coronary artery. The patient recovered and was discharged home after 7 days.

We used ab initio molecular dynamics simulations to compare the activation of 2-propanol on the low index Co3O4 (111), (110) and (001) surfaces in dry conditions. The thermal and surface assisted decomposition of a film of 2-propanol to 2-propoxide on the B-termination of each surface was monitored and analyzed. The investigations suggest an activity order of Co3O4 (111) > (110) > (001). On all surfaces, the Co3+ serve as adsorption sites. On the B-terminated (111) surface, full dissociation of all 2-propanol molecules at the interface is observed, accompanied by a Mars-van Krevelen-type mechanism upon pre-hydroxylation of the surface. The active regions show Co3+–O2-propoxide–Co2+ bridges where the coordinatively unsaturated Co2+ ions also participate in the adsorption and decomposition of 2-propanol. On the (110) surface, 2-propanol dissociation is driven by temperature, which activates the two-fold coordinatively unsaturated surface oxygens. The (001) surface on which almost no dissociation occurs is the least active. No formation of acetone is observed in the simulations conditions on all surfaces. [ABSTRACT FROM AUTHOR]

Despite the extensive use of 2-propanol and acetone in a wide range of applications in the chemical industry and in energy engineering, there is a lack of experimental data in the literature for their thermophysical properties including viscosity, interfacial tension, and density, especially at elevated temperatures beyond the respective normal boiling points. In the present study, the liquid viscosity and interfacial tension were determined simultaneously by surface light scattering (SLS) with average expanded uncertainties of (1.7 and 0.9)% at or close to saturation conditions for temperatures between (273 and 403) K. Furthermore, capillary viscometry (CV) and vibrating-tube densimetry were employed to measure the liquid viscosity at ambient pressure of 0.1 MPa from (283 to 353) K and the liquid density close to saturation conditions between (278 and 423) K. The obtained density data were used for the evaluation of both SLS and CV experiments. In comparison with literature data, the present density data show agreement for 2-propanol over the entire temperature range. In contrast, deviations of up to 0.5% at the maximum temperature can be found for acetone. For the viscosity and interfacial tension at low temperatures, agreement of the measurement results among each other and with literature data is mostly found. At elevated temperatures, the increasing deviations of the present experimental viscosity and interfacial tension data from recommended correlations indicate a lack of reliable data needed for their development. Overall, this work contributes to an improvement of the database for viscosity, interfacial tension, and density of 2-propanol and acetone over a wide temperature range up to 423 K. [ABSTRACT FROM AUTHOR]

The aim: implementation of the principles of green chemistry by regenerating the synthesis solvent 1,2,4-trichlorobenzene and reusing it during the synthesis of the Naphazoline nitrate substance. Study of the influence of the regenerated solvent on the quality of the final product by controlling analytical quality parameters. Development of a method for the quantitative determination and validation of synthesis solvents in a substance. Materials and methods: samples of the substance were synthesized according to the optimized proprietary technology of Farmak JSC. The obtained batches of fresh and regenerated 1,2,4-trichlorobenzene were analyzed according to the monograph of the European Pharmacopoeia on Naphazoline nitrate 0147. Results: the possibility of using regenerated 1,2,4-trichlorobenzene for the synthesis of the substance Naphazoline nitrate has been proven. It is shown that the regenerated solvent does not have a negative effect on the profile of impurities and the polymorphic form of the substance. Analytical quality parameters met the requirements of the internal specification and the requirements of the European Pharmacopoeia monograph. The developed and validated method of quantitative determination of synthesis solvents makes it possible to determine them at the required level. Conclusions: the introduction of regenerated 1,2,4-trichlorobenzene into the synthesis scheme made it possible to significantly reduce the amount of waste per 1 kg of product, which in turn significantly reduced the negative impact on the environment. Analytical quality parameters for regenerated 1,2,4-trichlorobenzene meet the requirements of the internal specification. Industrial series obtained on the regenerated solvent meet the requirements of the monograph of the European Pharmacopoeia. The polymorphic form of the substance batches manufactured on regenerated 1,2,4-trichlorobenzene corresponds to the polymorphic form of the substance batches manufactured on the fresh solvent. The obtained results on the influence of the regenerated solvent on the profile of impurities in the finished substance show the similarity of the profile of the series manufactured on both solvents. According to the requirements of ICH Q3C Impurities: Guideline for residual solvents, a method for quantitative determination of the residual content of 1,2,4-trichlorobenzene in the final product by gas chromatography was developed and validated. The absence of synthesis solvents at the limit of detection is shown. [ABSTRACT FROM AUTHOR]

Objectives: This study assessed the effect of chlorhexidine (CHX) and isopropyl alcohol (IA) on immediate and late pushout bond strength (PBS) of fiber posts to dentin. Materials and Methods: In this in vitro study, 54 single-canal premolars were endodontically treated, and randomly assigned to 3 groups (N=18) for root dentin conditioning with distilled water (control), 2% CHX, and 70% IA after post space preparation. Fiber posts were cemented with TheraCem self-adhesive cement, and each group was subdivided into two subgroups (N=9) for PBS measurement immediately after bonding, and after 5000 thermal cycles (5-55°C). The roots were then sectioned, and their PBS was measured. The mode of failure was evaluated under a stereomicroscope at ×40 magnification. Data were analyzed by repeated measures ANOVA and Tukey’s test (alpha=0.05). Results: The highest PBS was noted in the IA group (21.12 MPa) after 24 hours and the lowest PBS belonged to the control group after thermocycling (7.48 MPa). The immediate and post-thermocycling PBS were significantly lower in the control group than the CHX group (P

Experimental design methodology (EDM) was coupled with an artificial neural network (ANN) to predict and optimize the synthesis of isopropyl acetate over Nb2O5. The coupled model was compared to the empirical correlation of EDM, which correlates the conversion of acetic acid in isopropyl acetate (output variable) to reaction temperature, catalyst loading, and molar ratio of acetic acid/2-propanol (input variables). A key advantage of ANN is adding the reaction time to the input variables. The optimal ANN architecture was [5 5 5] with Bayesian regularization backpropagation as the network training algorithm. The experimental conversion has shown a good correlation with the predicted conversion for both training and test datasets, justifying the use of ANN. Statistical metrics showed that EDM coupled with ANN can better predict the conversion of acetic acid when compared to the empirical correlation (R2 = 0.9992 and SSE = 0.0285). Shapley values were applied in the ANN interpretability and ranked the input variables in descending order of importance: reaction temperature > reaction time > molar ratio of acetic acid/2-propanol > catalyst loading. [ABSTRACT FROM AUTHOR]

Deep proteome coverage in bottom-up proteomics requires peptide-level fractionation to simplify the complex peptide mixture before analysis by tandem mass spectrometry. By decreasing the number of coeluting precursor peptide ions, fractionation effectively reduces the complexity of the sample leading to higher sample coverage and reduced bias toward high-abundance precursors that are preferentially identified in data-dependent acquisition strategies. To achieve this goal, we report a bead-based off-line peptide fractionation method termed CIF or carboxylate-modified magnetic bead-based isopropanol gradient peptide fractionation. CIF is an extension of the SP3 (single-pot solid phase-enhanced sample preparation) strategy and provides an effective but complementary approach to other commonly used fractionation methods including strong cation exchange and reversed phase-based chromatography. We demonstrate that CIF is an effective offline separation strategy capable of increasing the depth of peptide analyte coverage both when used alone or as a second dimension of peptide fractionation in conjunction with high pH reversed phase. These features make it ideally suited for a wide range of proteomic applications including the affinity purification of low-abundance bait proteins.

Vapor pressures and other thermodynamic properties of liquids, such as density and enthalpy of mixtures, are the key parameters in chemical engineering for designing new process units, and are also essential for understanding the physical chemistry, macroscopic and molecular behavior of fluid systems. In this work, vapor pressures between 278.15 and 323.15 K, densities and enthalpies of mixtures between 288.15 and 318.15 K for the binary mixture (2-propanol + 1,8-cineole) have been measured. From the vapor pressure data, activity coefficients and excess Gibbs energies were calculated via the Barker's method and the Wilson equation. Excess molar volumes and excess molar enthalpies were also obtained from the density and calorimetric measurements. Thermodynamic consistency test between excess molar Gibbs energies and excess molar enthalpies has been carried out using the Gibbs–Helmholtz equation. Robinson–Mathias, and Peng–Robinson–Stryjek–Vera together with volume translation of Peneloux equations of state (EoS) are considered, as well as the statistical associating fluid theory that offers a molecular vision quite suitable for systems having highly non-spherical or associated molecules. Of these three models, the first two fit the experimental vapor pressure results quite adequately; in contrast, only the last one approaches the volumetric behavior of the system. A brief comparison of the thermodynamic excess molar functions for binary mixtures of short-chain alcohol + 1,8-cineole (cyclic ether), or +di-n-propylether (lineal ether) is also included. [ABSTRACT FROM AUTHOR]

Cosolvency is a widely used method employed to enhance drug solubility. There are limited data on the solubility of atorvastatin calcium (ATC). The aim of this work is to determine ATC solubility in glycerol + water and 2-propanol + water mixtures at several temperatures (293.15, 298.15, 303.15, 308.15 and 313.15 K). The apparent thermodynamic properties of the ATC dissolution process including Gibbs free energy (ΔG°sol), enthalpy (ΔH°sol) and entropy (ΔS°sol) were calculated. The ATC solubility in various concentrations of the anionic, cationic and non-ionic surfactant was explored. The drug is most efficiently dissolved in sodium lauryl sulphate (SLS). Tween 20 did not cause any increment in drug solubility. Benzalkonium chloride may form an insoluble salt with ATC anion resulting in a decrease in drug solubility. Cosolvency data were correlated by Jouyban–Acree and Jouyban–Acree–van't Hoff equation. [ABSTRACT FROM AUTHOR]

Magnetic-field effect on heterogenous photocatalysis was investigated on Pt/TiO2 by photocatalytic oxidation of 2-propanol. Two-level factorial design of dissolved oxygen concentration (DO), temperature, and magnetic flux density was applied for the first time. The high magnetic flux density with high DO significantly enhanced 22% 2-propanol oxidation. The singlet-triplet intersystem crossing of radicals, as well as the Lorentz force suppressing the recombination of photogenerated electrons and holes, enabled such an extraordinary magnetic effect. Moreover, paramagnetic oxygen and platinum on TiO2 reinforced the intersystem crossing, which contributed to the significant improvement of photocatalytic oxidation of 2-propanol under magnetic field.

The preparation method can considerably affect the structural, morphological, and gas-sensing properties of mixed-oxide materials which often demonstrate superior photocatalytic and sensing performance in comparison with single-metal oxides. In this work, hybrids of semiconductor nanomaterials based on TiO2 and ZnO were prepared by laser ablation of Zn and Ti plates in water and then tested as chemiresistive gas sensors towards volatile organics (2-propanol, acetaldehyde, ethanol, methanol) and ammonia. An infrared millisecond pulsed laser with energy 2.0 J/pulse and a repetition rate of 5 Hz was applied to Zn and Ti metal targets in different ablation sequences to produce two nano-hybrids (TiO2/ZnO and ZnO/TiO2). The surface chemistry, morphology, crystallinity, and phase composition of the prepared hybrids were found to tune their gas-sensing properties. Among all tested gases, sample TiO2/ZnO showed selectivity to ethanol, while sample ZnO/TiO2 sensed 2-propanol at room temperature, both with a detection limit of ~50 ppm. The response and recovery times were found to be 24 and 607 s for the TiO2/ZnO sensor, and 54 and 50 s for its ZnO/TiO2 counterpart, respectively, towards 100 ppm of the target gas at room temperature. [ABSTRACT FROM AUTHOR]

Metal oxide gas sensors are of great interest for applications ranging from lambda sensors to early hazard detection in explosive media and leakage detection due to their superior properties with regard to sensitivity and lifetime, as well as their low cost and portability. However, the influence of ambient gases on the gas response, energy consumption and selectivity still needs to be improved and they are thus the subject of intensive research. In this work, a simple approach is presented to modify and increase the selectivity of gas sensing structures with an ultrathin polymer thin film. The different gas sensing surfaces, CuO, Al2O3/CuO and TiO2 are coated with a conformal < 30 nm Poly(1,3,5,7-tetramethyl-tetravinyl cyclotetrasiloxane) (PV4D4) thin film via solvent-free initiated chemical vapor deposition (iCVD). The obtained structures demonstrate a change in selectivity from ethanol vapor to 2-propanol vapor and an increase in selectivity compared to other vapors of volatile organic compounds. In the case of TiO2 structures coated with a PV4D4 thin film, the increase in selectivity to 2-propanol vapors is observed even at relatively low operating temperatures, starting from >200 °C. The present study demonstrates possibilities for improving the properties of metal oxide gas sensors, which is very important in applications in fields such as medicine, security and food safety. [ABSTRACT FROM AUTHOR]

The approval of ethanol by the Biocidal Products Regulation has been under evaluation since 2007 due to controversial opinions on the risk assessment. Because of this critical situation, 2022 a memorandum was published to verify whether the use of ethanol for hand antisepsis poses any hazard. On the basis of the memorandum a toxicological evaluation of ethanol-based hand rubs is given. [ABSTRACT FROM AUTHOR]

The ability to predict the behaviour of high-pressure mixtures of carbon dioxide and alcohol is important for industrial purposes. The equilibrium composition of three binary carbon dioxide-alcohol systems was measured at temperatures of 313.15 K and 333.15 K and at pressures of up to 100 bar for carbon dioxide-2-propanol, up to 160 bar for carbon dioxide-1-butanol and up to 150 bar for carbon dioxide-2-butanol. Different equilibrium compositions of carbon dioxide in alcohols were observed despite their similar molecular weight (M2-propanol = 60.100 g mol−1, M1-butanol = 74.121 g mol−1 and M2-butanol = 74.122 g mol−1) and place in the functional hydroxyl group (first or second carbon molecule). It is assumed that the differences in the phase equilibria are due to different vapor pressures, polarities and solute-solute interactions. [ABSTRACT FROM AUTHOR]

Transfer hydrogenation (TH) is considered as one of the most promising ways to convert biomass into valuable products. This study aims to demonstrate the performance of high-loaded Ni-based catalysts in the TH of phenolic compounds such as guaiacol and dimethoxybenzenes. The experiments were carried out under supercritical conditions at 250 °C using 2-PrOH as the only hydrogen donor. Ni-SiO2 and NiCu-SiO2 were synthesized using the eco-friendly original method based on supercritical antisolvent coprecipitation. It has been found that guaiacol is rapidly converted into 2-methoxycyclohexanol and cyclohexanol, while the presence of Cu impedes the formation of the latter product. Transformations of dimethoxybenzene position isomers are slower and result in different products. Thus, 1,3-dimethoxybenzene loses oxygen atoms transform into methoxycyclohexane and cyclohexanol, whereas the saturation of the aromatic ring is more typical for other isomers. The Cu addition increases specific catalytic activity in the TH of 1,2-and 1,3-dimethoxybenzene compared to the Cu-free catalyst. [ABSTRACT FROM AUTHOR]

Binary Ni–Cu heterogeneous catalysts are known to demonstrate excellent activity in conventional hydrogenation of phenolic compounds, and Cu addition facilitates hydrodeoxygenation (HDO). In this study, we aimed to show the effect of Cu on the specific catalytic activity and selectivity of Ni–Cu catalysts in transfer hydrogenation, in which 2-PrOH was used as a solvent and an H donor. Catalytic transformations of anisole were studied in sub- and supercritical alcohol at 150 and 250 °C. The catalysts were prepared using an environmentally friendly supercritical antisolvent coprecipitation method, which makes it possible to obtain well-dispersed particles (less than 7 nm) at high metal loading (up to 50 wt.%). When copper is added, deactivation of the catalyst in transformations of anisole, including HDO, is observed. The experimental data and the appropriate kinetic analysis demonstrate that there is a decrease in the rate of anisole conversion accompanied by an increase in the concentration of acetone formed during the dehydrogenation of 2-PrOH. [ABSTRACT FROM AUTHOR]

Oxidation reactions are highly relevant transformation reactions in the industry. Mixed Co and Fe containing oxides are promising substituents for noble‐metal‐based catalysts due to lower cost and higher thermal stability. Performing oxidation catalysis in the liquid phase is desired to prevent total oxidation. An approach toward liquid phase reactions is water vapor added to the gas stream, which can help to build an experimental bridge between both phases. Here, nanocasted Co3‐xFexO4 spinels are studied in the gas phase oxidation of 2‐propanol as a probe for selective oxidation without and with the addition of water into the reaction feed. In both cases, low amounts of Fe (≤4 %) were found to be beneficial for the activity. Under wet conditions, there is a negative effect on the activity below 150 °C during heating due to competitive adsorption. However, at higher temperatures during cooling, the activity is higher due to a slower deactivation. [ABSTRACT FROM AUTHOR]

Statement of Problem: The outcome of photopolymerized 3-dimensional (3D) printing is influenced by the methods used for postprinting cleaning, yet information on postprinting cleaning is sparse., Purpose: The purpose of this in vitro study was to assess the cleaning efficiency and surface and mechanical properties of 3D printed resin according to postprinting cleaning methods., Material and Methods: Specimens were fabricated from a 3D model using resin materials (NextDent C&B MFH and DIOnavi-P. MAX) and were tested for postprinting cleaning methods for 5 minutes with isopropyl alcohol, isopropyl alcohol + ultrasonic, ethyl alcohol, ethyl alcohol + ultrasonic, and ultrasonic alone. Postpolymerization was followed for 5 minutes. The cleaning efficiency, microcomputed tomography (µCT), surface roughness, Vickers hardness, and flexural strength of the specimens were evaluated. The 1-way ANOVA test was performed after considering normality. A post hoc analysis with Bonferroni was also performed (α=.008 or.005)., Results: Ultrasonic in addition to cleaning solutions significantly improved the cleaning efficiency in NextDent C&B MFH specimens (P<.005), whereas ultrasonic did not affect the efficiency in DIOnavi-P. MAX specimens. No significant differences were found in surface roughness by postprinting cleaning methods in either NextDent C&B MFH or DIOnavi-P. MAX (P>.005). No significant changes in surface hardness were observed by postprinting cleaning methods (P>.008). In the NextDent C&B MFH, ethyl alcohol + ultrasonic significantly decreased the flexural strength (P<.005). There were no significant differences in the flexural strength in the DIOnavi-P. MAX (P>.005)., Conclusions: Ethyl alcohol was comparable with isopropyl alcohol for use as a postprinting cleaning solution for both NextDent C&B MFH and DIOnavi-P. MAX. The addition of ultrasonic to cleaning solutions should be applied with caution. These findings suggest that different postprinting cleaning methods can be recommended depending on the 3D printed resin materials., (Copyright © 2024 Editorial Council for The Journal of Prosthetic Dentistry. Published by Elsevier Inc. All rights reserved.)

It is pivotal to avoid cross-sample contamination in forensic genetic laboratories and optimal cleaning protocols for the removal of DNA are essential. A survey was performed, and ten forensic genetic laboratories shared their cleaning protocols in pre-PCR and post-PCR laboratories. The cleaning frequencies on different surface areas were somewhat similar, whereas none of the laboratories used the same cleaning reagents. Therefore, the efficiencies of the cleaning protocol utilised were tested and compared. The results showed that freshly made household bleach and Virkon® removed all amplifiable DNA from the surfaces, whereas DNA AWAY™ and the disinfection reagents ethanol, isopropanol, and ChemGene HLD 4 L did not., (© 2024. The Author(s).)

Introduction: Nausea and vomiting are common complaints among patients who refer to the emergency department with head trauma. This study aimed to compare the effect of aromatherapy with isopropyl alcohol versus intravenous ondansetron in management of mild head trauma nausea and vomiting. Methods: This randomized clinical trial was conducted on patients with isolated mild head trauma complaining of nausea and vomiting who were referred to emergency department during a 6-month period. Patients were randomly divided into control (IV ondansetron + aromatherapy with saline) and intervention (IV saline + aromatherapy with isopropyl alcohol) groups. The frequency of vomiting and the severity of nausea (from 0 to 100 with the verbal scaling) were written before, and 10 and 30 minutes after intervention and compared between groups. Results: A total of 210 patients (105 patients in each group) with a median age of 38 years were included in the study, 112 (54.3%) of which were male. Ten minutes after aromatherapy, no significant difference was observed in nausea and vomiting between the two groups (p >0.05). Nausea score after 30 minutes (p = 0.015) was significantly lower in the intervention group compared to the control group, but vomiting after 30 minutes (p

• CeO 2 , SrNiO 3 perovskite and their composites were prepared and characterized. • Composites with 15, 30, 50 and 70 % in mass of SrNiO 3 were used as photocatalysts. • 2-propanol oxidation in gas–solid was performed by simulated solar light or UV-LED. • The composite containing a 15 % of SrNiO 3 with CeO 2 was the most active. • Physical-chemical features of the composite account for photocatalytic activity. Both SrNiO 3 perovskite and CeO 2 are materials suitable for photocatalytic purposes. In this work, the preparation and physicochemical characterization of bare SrNiO 3 and CeO 2 along with composites where CeO 2 was enriched with the perovskite from 15 to 70 % in mass of SrNiO 3 in the composite are described. The materials have been used for the photocatalytic oxidation of 2-propanol in gas–solid regime in the presence of UV-LED or simulated solar irradiation. The solids were characterized by XRD, SEM/EDX, N 2 adsorption/desorption and FTIR and UV–Vis diffuse reflectance spectroscopies. The composite containing 15 % w/w of SrNiO 3 and 85 % w/w of CeO 2 resulted the most active, giving rise the complete degradation of 2-propanol after 1.5 h or 6.0 h of irradiation by UV-LED and simulated solar light irradiation, respectively. Photocatalytic activity results are discussed considering the physical–chemical properties on the catalysts. [ABSTRACT FROM AUTHOR]

We report an engineered strain of Escherichia coli that catabolizes the carbonaceous component of the extremely toxic chemical warfare agent sarin. Enzymatic decomposition of sarin generates isopropanol waste that, with this engineered strain, is then transformed into acetyl-CoA by enzymatic conversion with a key reaction performed by the acetone carboxylase complex (ACX). We engineered the heterologous expression of the ACX complex from Xanthobacter autotrophicus PY2 to match the naturally occurring subunit stoichiometry and purified the recombinant complex from E. coli for biochemical analysis. Incorporating this ACX complex and enzymes from diverse organisms, we introduced an isopropanol degradation pathway in E. coli, optimized induction conditions, and decoupled enzyme expression to probe pathway bottlenecks. Our engineered E. coli consumed 65% of isopropanol compared to no-cell controls and was able to grow on isopropanol as a sole carbon source. In the process, reconstitution of this large ACX complex (370 kDa) in a system naïve to its structural and mechanistic requirements allowed us to study this otherwise cryptic enzyme in more detail than would have been possible in the less genetically tractable native Xanthobacter system.

[Display omitted] • Developed metallic Cu NPs loaded ZIF-8 hybrid materials by impregnation method. • 11Cu(1.5 M)/ZIF-8 catalyzed transfer hydrogenation of furfural to 2-methylfuran. • Achieved > 99 % furfural conversion and 93.9 % 2-methylfuran (2-MF) selectivity. • Traced intriguing catalytic properties, responsible for higher 2-MF yield (93.7%) Catalytic transfer hydrogenation (CTH), that employs protic solvents as hydrogen sources to alleviate the use of molecular hydrogen H 2 , has gained great attention. This work, reports multifunctional, metallic Cu nanoparticles supported ZIF-8 material for CTH of furfural to a highly valued fuel additive, 2-methylfuran (2-MF) using 2-propanol. Of all as-synthesized xCu(yM)/ZIF-8 catalysts with varied NaBH 4 concentration (yM) and Cu loading (x), 11Cu(1.5 M)/ZIF-8 exhibited higher catalytic activity with > 99 % FAL conversion and 93.9 % 2-MF selectivity. This is ascribed to its high specific surface area, and existence of optimum amount of Lewis acid-base sites along with Cu0 species, which are responsible for hydrogenation of furfural to furfuryl alcohol and subsequent hydrogenolysis to produce 2-MF. The present work reports a highly efficient and stable, metal-MOF hybrid material for CTH of FAL to 2-MF, which is one among the best reports available in literature, therewith suggests a promising approach for bio-oil upgradation. [ABSTRACT FROM AUTHOR]

Objective: Studies indicate inhaled isopropyl alcohol (IIA) is effective or superior to ondansetron for adult patients. Although quick‐acting and low cost, it cannot be assumed this remedy is suitable for adoption in all settings. We explored how an innovative antiemetic remedy studied in the United States translates to a sub‐Saharan Africa clinic/hospital setting using Rogers' Diffusion of Innovation Framework. Design: Qualitative design with purposive sampling. Sample: Health care staff (n = 11) providing and community members (n = 22) accessing health care services in a sub‐Saharan Africa clinic/hospital. Measurements: Semi‐structured interviews with coding and identification of themes via deductive content analysis using Rogers' Diffusion of Innovation Framework. Results: Nausea and vomiting was a common complaint, with malaria the most common etiology. Participants emphasized treatment of etiology over symptomatic treatment and described previous aromatherapy use. IIA advantages included administration route, quick‐acting, self‐administration, portable, available, and easy trialability. Participants expressed concerns regarding use of term "alcohol" as potentially offensive to others. Conclusion: Use of Rogers' Diffusion of Innovation framework identified barriers and facilitators to translation of a novel antiemetic remedy for sub‐Saharan Africa clinic/hospital settings. Evaluating clinical innovations from perspectives of relative advantage, compatibility, complexity, trialability, and observability enhances adoption of innovations within clinical settings. [ABSTRACT FROM AUTHOR]

Many people convicted for drunken driving suffer from an alcohol use disorder and some traffic offenders consume denatured alcohol for intoxication purposes. Venous blood samples from people arrested for driving under the influence of alcohol were analyzed in triplicate by headspace gas chromatography (HS-GC) using three different stationary phases. The gas chromatograms from this analysis sometimes showed peaks with retention times corresponding to acetone, ethyl methyl ketone (2-butanone), 2-propanol, and 2-butanol in addition to ethanol and the internal standard (1-propanol). Further investigations showed that these drink-driving suspects had consumed an industrial alcohol (T-Red) for intoxication purposes, which contained > 90% w/v ethanol, acetone (~ 2% w/v), 2-butanone (~ 5% w/v) as well as Bitrex to impart a bitter taste. In n = 75 blood samples from drinkers of T-Red, median concentrations of ethanol, acetone, 2-butanone, 2-propanol and 2-butanol were 2050 mg/L (2.05 g/L), 97 mg/L, 48 mg/L, 26 mg/L and 20 mg/L, respectively. In a separate GC analysis, 2,3-butanediol (median concentration 87 mg/L) was identified in blood samples containing 2-butanone. When the redox state of the liver is shifted to a more reduced potential (excess NADH), which occurs during metabolism of ethanol, this favors the reduction of low molecular ketones into secondary alcohols via the alcohol dehydrogenase (ADH) pathway. Routine toxicological analysis of blood samples from apprehended drivers gave the opportunity to study metabolism of acetone and 2-butanone without having to administer these substances to human volunteers., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

The phototransformation of Oryzalin was studied under UV light (λmax ≥ 290 nm) and sunlight (λmax ≥ 250 nm) in aqueous isopropanol and acetonitrile solution in absence and presence of TiO2 as sensitizer. The rate of photodegradation of Oryzalin in different solvent system followed first-order kinetics, and calculated half-lives were found to be in the range of 23.52-53.75 h for UV light and 41.23-61.43 h for sunlight. From this study, total 12 photoproducts were identified and characterized on the basis of column chromatography and Q-Tof micromass spectral data. The plausible mechanism of phototransformation involved was hydrolysis, breaking of sulfonic bond, and loss of amino and sulfonic acid group.

The main purpose of this paper was to systematically investigate the influence of the solvent on mechanism behind O3 reaction with 2‐propanol. Gibbs energies were calculated for the reactions that initiated the possible mechanisms: hydride transfer ((H3C)2(HO)C–H(solv) + O3(solv) → (H3C)2(HO)C+(solv) + HO3−(solv)) and H‐abstraction ((H3C)2(HO)C–H(solv) + O3(solv) → (H3C)2(HO)C•(solv) + HO3•(solv)) under working conditions with various solvents. The characteristic of the solvent used for calculations was the relative dielectric constant, ɛ, which ranged from 2.02 (cyclohexane) to 80 (water). The calculation method was based on density functional theory (DFT). In addition, this study took into consideration the conversion of the radical pair as products of H‐abstraction to the ion pair formed following hydride transfer; the conversion occurred by electron transfer ((H3C)2(HO)C•(solv) + HO3•(solv) → (H3C)2(HO)C+(solv) + HO3−(solv)). Our calculations showed that the reaction of O3 with 2‐propanol was triggered by H‐abstraction in nonpolar solvents, but in polar solvents, mainly by a pseudo‐hydride transfer consisting of H‐abstraction followed by electron transfer between the radicals formed by H‐abstraction. The transition state formed en route to products had a linear structure for water, whereas for cyclohexane, linear and cyclic transition states coexisted. [ABSTRACT FROM AUTHOR]

Solubility and density profiles for 3-aminosalicylic acid (3-ASA) in the mixed solvents of 2-propanol and water is determined by a shake-flask method at 293.2–313.2 K. The obtained numerical data is correlated by some mathematical models such as van't Hoff, the mixture response surface, Jouyban–Acree, Jouyban–Acree–van't Hoff and the modified Wilson models. The accuracy of the used models is investigated by calculation of the mean relative deviations for back-calculated data. Moreover, apparent thermodynamic properties such as standard enthalpy, Gibbs free energy and entropy of the 3-ASA dissolution process are computed and discussed. Further, 3-ASA is preferentially solvated by water in almost all the aqueous mixtures. [ABSTRACT FROM AUTHOR]

Perovskites are interesting oxidation catalysts due to their chemical flexibility enabling the tuning of several properties. In this work, we synthesized LaFe1−xCoxO3 catalysts by co‐precipitation and thermal decomposition, characterized them thoroughly and studied their 2‐propanol oxidation activity under dry and wet conditions to bridge the knowledge gap between gas and liquid phase reactions. Transient tests showed a highly active, unstable low‐temperature (LT) reaction channel in conversion profiles and a stable, less‐active high‐temperature (HT) channel. Cobalt incorporation had a positive effect on the activity. The effect of water was negative on the LT channel, whereas the HT channel activity was boosted for x>0.15. The boost may originate from a slower deactivation rate of the Co3+ sites under wet conditions and a higher amount of hydroxide species on the surface comparing wet to dry feeds. Water addition resulted in a slower deactivation for Co‐rich catalysts and higher activity in the HT channel state. [ABSTRACT FROM AUTHOR]

[Display omitted] • CeO 2 with well-defined (1 0 0) and (1 1 1) facets are valuable model metal oxide catalysts to probe acid and base sites. • Morphology of CeO 2 nanoparticles affect the acid site properties regardless of oxygen defect density. • The CeO 2 (1 0 0) facet has stronger base sites leading to increased rates of 2-propanol dehydrogenation to acetone. • The CeO 2 (1 1 1) facet has stronger acid sites along with a higher acid site density which increase the rates of 2-propanol dehydration to propene. CeO 2 nanoshapes, cubes with dominant (1 0 0) facets and octahedra with dominant (1 1 1) facets, were synthesized to investigate the influence of surface structure on acid-base properties. An optimization of calcination temperatures, coupled with Raman and TEM, was employed to minimize the intrinsic (Frenkel-type) defect sites and their potential complications on the facet studies involved in this work. The acid-base properties of these CeO 2 nanoshapes were characterized with in situ pyridine and CO 2 adsorption using infrared spectroscopy and quantified using pyridine, ammonia, and CO 2 temperature-programmed desorption (TPD). The (1 0 0) facet displayed weaker acid sites with lower site density than the (1 1 1) facet which had a similar density of base sites but those on the (1 0 0) facet were stronger. A strong correlation was observed between 2-propanol conversion and each facet's acid-base properties. CeO 2 cubes exhibited greater base-site catalyzed dehydrogenation to acetone while the more acidic CeO 2 octahedra were more active in dehydration to propene. [ABSTRACT FROM AUTHOR]

It is known that mixtures of CTAB and NaSal form viscoelastic solutions. For a 100 mM CTAB solution and increasing NaSal concentration, the viscosity increases strongly at a concentration of 10 mM NaSal, reaches a maximum at 60 mM NaSal, decreases then to a minimum at 100 mM, and, on further, increases passes over a second maximum at a NaSal concentration of 220 mM. The changes of the viscosity at the first maximum, at the minimum, and at the second maximum are due to changes of the mechanism that effect the structural relaxation times while the shear modulus remains constant. On addition of 1-propanol to the solutions at the maximum and at the minimum, the viscosities decrease strongly to the viscosity slightly above water while the shear modulus in the viscous solution remains constant. The data can be explained by assuming that part of the 1-propanol adsorbs at the surface of the three-dimensional network that is formed from wormlike micelles and makes the hydrophobic surface hydrophilic. On addition of 2-propanol to the solutions at the first maximum, the viscosity decreases also at first up to a concentration of 4% 2-propanol. On further increase of 2-propanol, a second relaxation effect with a different relaxation time and a different shear modulus appear. The sum of the two moduli remains about the same as the shear modulus of the solution without isopropanol. The second relaxation effect can be explained by assuming that only one methyl group of 2-propanol binds to the surface of the network while the other one sticks into water. The surface remains therefore hydrophobic and parts of the network can bind to each other what gives rise to the second relaxation effect. [ABSTRACT FROM AUTHOR]

A thermal process was employed to prepare a catalyst consisting of a mixture of metallic-Pt and rutile RuO2 nanocrystals. This catalyst was used for the electrooxidation of 2-propanol in an alkaline solution. The effect of the catalyst composition on its microstructure, surface properties and catalytic activity was examined. With increasing the RuO2 content, the catalytic activity increases, reaches its maximum and then decreases. The catalytic effect is a result of the bifunctional mechanism of the mixture of Pt and RuO2 nanocrystals. The RuOHad particles are formed on Ru atoms of the RuO2 nanocrystals at potentials more negative than on Pt atoms. These oxy-species facilitate the dehydrogenation, breaking of C–C bonds and oxidation of both 2-propanol and its intermediates, adsorbed on assemblies of adjacent Pt atoms. [ABSTRACT FROM AUTHOR]

Infection control instructions call for use of alcohol-based hand rub solutions to inactivate severe acute respiratory syndrome coronavirus 2. We determined the virucidal activity of World Health Organization–recommended hand rub formulations, at full strength and multiple dilutions, and of the active ingredients. All disinfectants demonstrated efficient virus inactivation.

The preparation method can considerably affect the structural, morphological, and gas-sensing properties of mixed-oxide materials which often demonstrate superior photocatalytic and sensing performance in comparison with single-metal oxides. In this work, hybrids of semiconductor nanomaterials based on TiO2 and ZnO were prepared by laser ablation of Zn and Ti plates in water and then tested as chemiresistive gas sensors towards volatile organics (2-propanol, acetaldehyde, ethanol, methanol) and ammonia. An infrared millisecond pulsed laser with energy 2.0 J/pulse and a repetition rate of 5 Hz was applied to Zn and Ti metal targets in different ablation sequences to produce two nano-hybrids (TiO2/ZnO and ZnO/TiO2). The surface chemistry, morphology, crystallinity, and phase composition of the prepared hybrids were found to tune their gas-sensing properties. Among all tested gases, sample TiO2/ZnO showed selectivity to ethanol, while sample ZnO/TiO2 sensed 2-propanol at room temperature, both with a detection limit of ~50 ppm. The response and recovery times were found to be 24 and 607 s for the TiO2/ZnO sensor, and 54 and 50 s for its ZnO/TiO2 counterpart, respectively, towards 100 ppm of the target gas at room temperature.

The interaction between organic molecules and oxidized catalyst surfaces has frequently been used to study the fuel crossover from the anode to the cathode in direct liquid fuel cells. In such experiments, the oxidized surface is put in contact with the fuel under open circuit conditions, and the evolution of the potential is registered. The open circuit potential (OCP) vs. time features can then inform on the reactivity of the fuel with the oxidized surface and provide valuable information not only to applications in fuel cells but also to the electrochemical reform of those molecules to produce clean hydrogen. In this paper, we present an experimental investigation of the open circuit interaction between ethanol or 2-propanol with oxidized platinum surfaces. Besides the OCP time traces, we have also employed cyclic voltammetry and fast oxide reduction sweep in the presence of the alcohols. Comparable reaction currents are obtained in the cyclic voltammogram, but the electro-oxidation of 2-propanol sets in at considerably lower overpotentials than that of ethanol. At the high potential region, both the magnitude and the potential of the current peak are nearly identical in both cases. In contrast, under open circuit conditions, the interaction of ethanol with the oxidized platinum surface is more pronounced than that found for 2-propanol, and these results are corroborated by the facile reduction of the platinum oxides along the fast backward sweep for the case of the latter., (© 2024 Wiley-VCH GmbH.)

Aim: To systematically examine the sample suitability and stability for volatile alcohols (methanol, ethanol and isopropanol with its metabolite acetone) and glycols (ethylene/propylene glycols, EG/PG) in different collection tubes., Method: Two pools of whole blood were created and spiked with two levels of volatile alcohols and EG/PG. The spiked whole blood was added to six different blood collection tubes and were kept at different storage conditions. An aliquot was prepared from baseline replicates. Concentrations of volatile alcohols and glycols were analysed by gas chromatography., Results: All blood collection tubes have demonstrated similar performance over different storage conditions, that is, to be statistically insignificant (p>0.05) with the only exception of PG at the high concentration of day 7 at 4°C condition (p<0.05 but clinically insignificant as

Background: Alcohol poisoning is a significant global problem that has become an epidemic. The determination of the alcohol type is hereby essential as it may affect the course of the treatment; however, there is no routine laboratory diagnostic method for alcohol types other than for ethanol. In this study, we aimed to define a simple method for alcohol type differentiation by utilizing a combination of breathalyzer and spectrophotometrically measured serum ethanol results., Methods: A breathalyzer and spectrophotometry were used to measure four different types of alcohol: ethanol, isopropanol, methanol, and ethylene glycol. To conduct serum alcohol analysis, four serum pools were created, each containing a different type of alcohol. The pools were analyzed using the spectrophotometric method with an enzymatic ethanol test kit. An experiment was conducted to measure the different types of alcohol using impreg-nated cotton and a balloon, simulating a breathalyzer test. An algorithm was created based on the measurements., Results: Based on the results, the substance consumed could be methanol or isopropanol if the breathalyzer test indicates a positive reading and if the blood ethanol measurement is negative. If both the breathalyzer and the blood measurements are negative, the substance in question may be ethylene glycol., Conclusions: This simple method may determine methanol or isopropanol intake. This straightforward and innovative approach could assist healthcare professionals in different fields with diagnosing alcohol intoxication and, more precisely, help reducing related morbidity and mortality.

Introduction: One of the important problems that lower the diagnostic value of blood culture is contamination with skin organisms. The povidone-iodine, alcohol, and chlorhexidine gluconate alcohol are used for disinfection prior to blood sampling for culture., Methods: The investigator-initiated, open label, single centre, randomised trial compared blood culture contamination rates between two groups of patients in which using a povidone iodine skin-preparation process with the contamination rate for using "2 % chlorhexidine with 70 % isopropyl alcohol" skin-disinfection. The patients who required sampling for blood cultures were included in the study and study period was from 15 March 2023 to 15 July 2023., Results: A total of 400 blood cultures were obtained during the study, including 133 in the study group and 267 in the control group. In the total blood cultures, 11.75 % (n = 47) had microorganism isolation. Among them 39 (9.75 %) were contaminants and 8 (2 %) of them were true pathogens. The contaminant microorganisms were as following; 34 coagulase-negative Staphylococci, 3 Micrococcus spp, and 2 Streptococci viridans. The blood culture contamination rate in the study group was 5.3 % (n = 7) and 12.0 % (n = 32) in the control group, and significantly lower in the study group (p = 0.033). There is no significant difference regarding skin related side effects between two groups., Conclusions: This study, showed that 2 % chlorhexidine gluconate in 70 % isopropyl alcohol is more efficacious in children than 10 % povidone-iodine preparations for disinfecting the skin prior to blood specimen collection for prevention of blood culture contamination., Competing Interests: Declaration of competing interest The authors have no example conflict of interest and no relevant financial relationships to disclose. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors., (Copyright © 2023 Japanese Society of Chemotherapy, Japanese Association for Infectious Diseases, and Japanese Society for Infection Prevention and Control. Published by Elsevier Ltd. All rights reserved.)

[Display omitted] • TH of mono-, di- and trinuclear aromatic compounds was studied at 150 °C and 82 °C • 2-PrOH/Raney® nickel combination demonstrates a high reactivity • Naphthalene and biphenyl are partially reduced at 82 °C with high selectivity • Trinuclear anthracene and phenanthrene at 150 °C are hydrogenated into octahydro-derivatives Catalytic hydrogenation of mono-, di- and trinuclear aromatic compounds has been studied under hydrogen transfer conditions at 150 °C and 82 °C in 2-PrOH as a hydrogen donor and with Raney® nickel as a catalyst. In contrast to conjugated or condensed aromatic rings, isolated ones demonstrated low reactivity in transfer hydrogenation (TH) that can be used to increase the hydrogenation selectivity of the reaction. So, naphthalene and biphenyl are partially hydrogenated into tetralin and cyclohexylbenzene, respectively, with excellent conversion (≥ 96 %) and selectivity (≥ 98 %) for 5–6 h at 82 °C. Increasing the reaction temperature to 150 °C results expectedly in the hydrogenation of second aromatic ring, which occurs slowly enough. Only 8 % of decaline and 42 % of dicyclohexyl, correspondingly, were obtained after 5 h at 150 °C. At the same time, TH of trinuclear anthracene and phenanthrene at 150 °C resulted in the formation of deeper hydrogenated octahydro-anthracenes and -phenanthrenes, respectively. [ABSTRACT FROM AUTHOR]

The hydrogenolysis of 1-phenylethanol over supported palladium catalyst (Pd/SiO2, Pd/C, Pd/Al2O3, Pd/MgO, or Pd/hydroxyapatite) in 2-propanol under reflux conditions (82 °C) was investigated. The effects of nine diffrent acid additives (formic acid, acetic acid, lactic acid, pyruvic acid, oxalic acid, malonic acid, succinic acid, malic acid, or p-toluenesulfonic acid) were also examined. Ethylbenzene and acetophenone were both produced in the presence of the acid additives; however, only acetophenone was produced in the absence of acid additive. Selectivity for ethylbenzene tended to increase with increasing acid strength of the additive, although there were some exceptions. The highest ethylbenzene selectivity (73.6%) was achieved over Pd/C catalyst in the presence of formic acid, and moderate selectivity (43–46%) was achieved over all of the Pd catalysts in the presence of oxalic acid. Deuterium-labeling experiments revealed a reaction pathway involving a hydrogen-transfer process, in which 2-propanol, formic acid, and 1-phenylethanol function as hydrogen donors. [ABSTRACT FROM AUTHOR]

Intermittency of Lagrangian velocity and acceleration is a key to understanding transport in complex systems ranging from fluid turbulence to flow in porous media. High-resolution optical particle tracking in a three-dimensional (3D) porous medium provides detailed 3D information on Lagrangian velocities and accelerations. We find sharp transitions close to pore throats, and low flow variability in the pore bodies, which gives rise to stretched exponential Lagrangian velocity and acceleration distributions characterized by a sharp peak at low velocity, superlinear evolution of particle dispersion, and double-peak behavior in the propagators. The velocity distribution is quantified in terms of pore geometry and flow connectivity, which forms the basis for a continuous-time random-walk model that sheds light on the observed Lagrangian flow and transport behaviors.

There still is an unmet need for a safe and sustained intravitreal drug delivery system. In this study we are proposing and characterizing a micelle based, clear-media intravitreal drug delivery system using the lipid derivatized nucleoside analog, hexadecyloxypropyl-cidofovir (HDP-CDV, CMX 001). HDP-CDV forms micelles in water and in vitreous supernatant with the critical micelle concentration of 19 μg/mL and 9 μg/mL, respectively at 37 °C. The formed micelles had the average size of 274.7 nm and the Zeta potential of -47.1 mV. Drug release study in the excised rabbit vitreous showed a sustained release profile with a half-life of 2.7 days. The micelle formulation of HDP-CDV demonstrated a good safety profile in two animal species (rabbit and guinea pig) following intravitreal injection. The sustained efficacy was tested in a pretreatment study design and the drug potency was tested in an ongoing herpes simplex virus (HSV-1) retinitis model. The pretreatment studies using single intravitreal injection and later HSV-1 infection revealed at least 9 weeks of vitreous presence and therapeutic level of HDP-CDV, with 71% eyes protection from infection. The treatment study demonstrated that intravitreal administration halted active HSV-1 retinitis in 80% of the infected eyes while cidofovir (CDV) treatment failed to suppress active HSV-1 retinitis. In summary, lipid derivatized nucleoside analogs can be formulated as a micelle intravitreal injection and provides a sustained drug release in vitreous for chronic retinal diseases.

The ability to predict the behaviour of high-pressure mixtures of carbon dioxide and alcohol is important for industrial purposes. The equilibrium composition of three binary carbon dioxide-alcohol systems was measured at temperatures of 313.15 K and 333.15 K and at pressures of up to 100 bar for carbon dioxide-2-propanol, up to 160 bar for carbon dioxide-1-butanol and up to 150 bar for carbon dioxide-2-butanol. Different equilibrium compositions of carbon dioxide in alcohols were observed despite their similar molecular weight (M2-propanol = 60.100 g mol−1, M1-butanol = 74.121 g mol−1 and M2-butanol = 74.122 g mol−1) and place in the functional hydroxyl group (first or second carbon molecule). It is assumed that the differences in the phase equilibria are due to different vapor pressures, polarities and solute-solute interactions.

Background: The use of disinfectants is part of the everyday life of people, especially in the medical profession. During the coronavirus disease 2019 (COVID-19) pandemic, the use of disinfectants continues to increase and is of fundamental importance in infection control. Objectives: To determine the frequency of sensitization and the value of patch testing to didecyldimethylammonium chloride (DDAC) and the alcohols ethanol, 1-propanol, and isopropanol. Methods: Clinical patch test data of 145 patients with suspected contact allergy to disinfectants were retrospective analysed. Results: Among the 145 patients patch tested with the different alcohols, only one nurse was detected with a possible allergy to 1-propanol. Additional patch testing in 84 patients with DDAC 0.05% resulted in five patients with weakly positive reactions only, without clinical relevance. Patch testing with DDAC 0.03% showed no positive reactions at all on day 3 readings. Conclusions: DDAC and alcohols are rarely responsible for allergic contact dermatitis. The accused products of the patients should be checked for other allergens and further additives with skin-irritating properties. Individual susceptibility and mishandling of the disinfectants should be considered. [ABSTRACT FROM AUTHOR]