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Background: The aim of this study was to evaluate the impact of intravenous palonosetron compared to ondansetron on hypotension induced by spinal anesthesia in women undergoing cesarean section. Methods: Fifty-four women scheduled for elective cesarean section were, randomly allocated to ondansetron group (n = 27) or palonosetron group (n = 27). Ten minutes prior to the administration of spinal anesthesia, participants received an intravenous injection of either ondansetron or palonosetron. A prophylactic phenylephrine infusion was initiated immediately following the intrathecal administration of bupivacaine and fentanyl. The infusion rate was titrated to maintain adequate blood pressure until the time of fetal delivery. The primary outcome was total dose of phenylephrine administered. The secondary outcomes were nausea or vomiting, the need for rescue antiemetics, hypotension, bradycardia, and shivering. Complete response rate, defined as the absence of postoperative nausea and vomiting and no need for additional antiemetics, were assessed for up to 24 hours post-surgery. Results: No significant differences were observed in the total dose of phenylephrine used between the ondansetron and palonosetron groups (387.5 μg [interquartile range, 291.3–507.8 μg versus 428.0 μg [interquartile range, 305.0–507.0 μg], P = 0.42). Complete response rates also showed no significant differences between the groups both within two hours post-spinal anesthesia (88.9% in the ondansetron group versus 100% in the palonosetron group; P = 0.24) and at 24 hours post-surgery (81.5% in the ondansetron group versus 88.8% in the palonosetron group; P = 0.7). In addition, there was no difference in other secondary outcomes. Conclusion: Prophylactic administration of palonosetron did not demonstrate a superior effect over ondansetron in mitigating hemodynamic changes or reducing phenylephrine requirements in patients undergoing spinal anesthesia with bupivacaine and fentanyl for cesarean section. [ABSTRACT FROM AUTHOR]

Highlights • One-step SPLE extraction method for PAHs, OCPs and PCBs in PM2.5 was developed. • Seventeen PAHs, 20 OCPs, and 63 PCBs showed a low LOQ and good recoveries. • Dozens of PAHs and several OCPs and PCBs were detected from ambient PM2.5 in Korea. • Newly developed method is cost-effective to analyze massive PM2.5 samples. Abstract Studies investigating toxic organic pollutants in fine dust (PM2.5), such as polycyclic aromatic hydrocarbons (PAHs), organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs), are insufficient, despite the pollutants' potent toxicity. The objective of this study is to develop an analytical method for determining PAHs, OCPs and PCBs in ambient PM2.5 using selective pressurized liquid extraction (SPLE). To maximize the extraction efficiency of target analytes, the extraction parameters of SPLE, particularly solvent type, temperature, static time, and cycle number, were optimized. The highest recoveries were observed under the conditions of dichloromethane:acetone (9:1), 100℃, 5 min of static time, and 1 cycle extraction, which is selected as the optimal method of SPLE. In the method validation, the results showed that the suggested method can quantify 17 PAHs, 20 OCPs, and 63 PCBs in PM2.5. Using urban dust SRM (1648a) and ambient PM2.5 samples, the applicability of the method was also confirmed. Total concentration of PAHs was the highest (2639.42–7377.75 pg/m3) followed by OCPs (80.57–674.69 pg/m3) and PCBs (1.39–9.34 pg/m3). Most of the PAHs were detected, whereas 2–7 compounds among 20 OCPs and 2–6 compounds among 63 PCBs were determined. The developed analytical method is highly efficient in terms of process (a one-step extraction process), time (15 min extraction time per one sample) and solvent usage (less than 30 mL per one sample), showing good performance. This method can be applied to investigate the organic toxicants in PM2.5, and it can contribute to monitoring and risk assessment, leading to an effective risk management policy for PM2.5 in Korea. [ABSTRACT FROM AUTHOR]

Citrate-coated AgNPs (c-AgNPs) have negatively charged surfaces and their surface interactions with heavy metals can affect metal toxicity in aquatic environments. This study used Daphnia magna to compare the acute toxicities and bioaccumulation of As(V), Cd, and Cu when they interact with c-AgNPs. The 24-h acute toxicities of As(V) and Cu were not affected by the addition of c-AgNPs, while bioaccumulation significantly decreased in the presence of c-AgNPs. In contrast, both the 24-h acute toxicity and bioaccumulation of Cd increased in the presence of c-AgNPs. These toxicity and bioaccumulation trends can be attributed to the interactions between the AgNP surface and the heavy metals. As(V) and c-AgNPs compete by negative charge, decreasing As(V) toxicity. Copper adheres readily to c-AgNP citrate, decreasing Cu bioavailability, and thus reducing Cu toxicity and bioaccumulation. Citrate complexes with divalent cations such as Ca and Mg reduce the competition between divalent cations and Cd on biotic ligand, increasing toxicity and bioaccumulation of Cd. This study shows that surface properties determine the effect of c-AgNPs on heavy metal toxicities and bioaccumulations; hence, further studies on the effect of nanoparticle by it surface properties are warranted. [ABSTRACT FROM AUTHOR]

Simple Summary: This study proposed a methodology to simulate ecological damage in a toluene spill situation by coupling AQUATOX, an established ecological assessment model, and EFDC, a Lagrangian fluid diffusion model. TheAQUATOX-EFDC simulation showed a significant ecological impact, especially the greatest damage on the fish species group, the top predators. In this study, an ecological impact was assessed for the short-term leak scenario through the AQUATOX-EFDC model, which combines the proven ecological model AQUATOX with the hydrodynamic model EFDC. A case study of the coupled AQUATOX-EFDC model was conducted for 30–30,000 kg toluene leak scenarios in the Jeonju River in South Korea. A 21-day scenario simulation was conducted, and the impact of the toluene spill accident was evaluated by comparing the biomass between the control simulation and the perturbed simulation. As a result of the simulation, it was found that in the scenario in which 3000 kg of toluene was leaked for a day, a substantial change was expected in the range of 0–640 m from the accident site. Additionally, for a 30,000 kg leak, a substantial change was expected in the range of 0–2300 m from the accident site, and the greatest damage was observed for the fish species group, the top predators. As a result, the AQUATOX-EFDC simulation showed a significant ecological impact, and the proposed model will be helpful to understand the ecological impact and establish the management strategy for the ecological risk of the chemical spill. [ABSTRACT FROM AUTHOR]

Guanyl-urea phosphate (GUP) was introduced into furfurylated wood in order to improve fire retardancy. Modified wood was produced via vacuum-pressure impregnation of the GUP–furfuryl alcohol (FA) aqueous solution, which was then polymerized at elevated temperature. The water leaching resistance of the treated wood was tested according to European standard EN 84, while the leached water was analyzed using ultra-performance liquid chromatography (UPLC) and inductively coupled plasma–sector field mass spectrometry (ICP-SFMS). This new type of furfurylated wood was further characterized in the laboratory by evaluating its morphology and elemental composition using optical microscopy and electron microscopy coupled with energy-dispersive X-ray spectrometry (SEM-EDX). The chemical functionality was detected using infrared spectroscopy (FTIR), and the fire resistance was tested using cone calorimetry. The dimensional stability was evaluated in wet–dry soaking cycle tests, along with the mechanical properties, such as the Brinell hardness and bending strength. The fire retardancy of the modified furfurylated wood indicated that the flammability of wood can be depressed to some extent by introducing GUP. This was reflected in an observed reduction in heat release rate (HRR2) from 454.8 to 264.9 kW/m2, without a reduction in the material properties. In addition, this leaching-resistant furfurylated wood exhibited higher fire retardancy compared to conventional furfurylated wood. A potential method for producing fire-retardant treated furfurylated wood stable to water exposure has been suggested. [ABSTRACT FROM AUTHOR]

A large quantity of volatile organic compounds (VOCs) can be released into water environments from oil spills and chemical exposure accidents. A recently developed solid ceramic dosimeter (SCD) could be used for long-term measuring of low VOCs concentrations in water. However, calibration and field testing of these SCDs have thus been far insufficient to apply for VOCs monitoring in a water environment in a chemical industrial area. We conducted laboratory calibration experiments and stability tests of the SCD. The mass accumulation of 14 target VOCs from 2 to 100 μg/L was increased linearly with time in the sampler. The absorption rate of the VOCs was related to Henry's law constant. The average diffusion coefficient of the 14 VOCs in the SCD wall was 1.02 × 10−9 m2/s. The SCD was utilized in a petrochemical plant complex in South Korea with an industrial wastewater reservoir. After a total of 7 days of deployment, chloroform, ethylbenzene, and toluene were detected by both passive sampling and grab sampling at the same VOC concentrations. [ABSTRACT FROM AUTHOR]

Increasing evidence suggests that the toxicity of fine dust particles (PM 2.5) is linked to specific components rather than their mass. However, research on the chemical composition and health risk of PM 2.5 is insufficient. This study analyzed the metals, polycyclic aromatic hydrocarbon (PAHs), organochlorine pesticides (OCPs), and polychlorinated biphenyls (PCBs) present in PM 2.5 and evaluated their risk to health during outdoor activities. The concentration of metals was one order of magnitude higher than that of PAHs and the concentration and detection frequency of OCPs and PCBs were considerably lower than those of metals and PAHs. The lifetime excess cancer risk (LECR) for carcinogens in PM 2.5 exceeded de minimis risk (1 × 10−6) as 1.33–3.44 × 10−6 (at 5th–95th percentile) as Cr(VI), As, and Cd showed high contributions. Children in the 2 < years <18 age group had a high risk of cancer due to early-life susceptibility. The proportion of ∑Metals to LECR was approximately 95%, while ∑PAHs attributed to 5% of total LECR. The effects of ∑OCPs and 2,3′,4,4′,5′-Pentachlorobiphenyl (PCB-123) on LECR were negligible. The hazard quotient (HQ) for non-carcinogens was <1, and non-carcinogenic effects were not expected. Mn, BaP, Pb, As, and Cd were the key determinants of the HQ values and among the identified PM 2.5 sources they are closely related to industrial activities, oil combustion, and gasoline exhaust. Therefore, control strategies for these sources can effectively reduce PM 2.5 risk. This study measured the concentrations of toxic compounds in ambient PM 2.5 and considered only PM 2.5 exposure during outdoor activities. PM 2.5 health risk during the entire day would be higher than the PM 2.5 risk determined in this study, and further research is required for this evaluating this risk. Unlabelled Image • LECR was 1.33–3.44 × 10−6 (5th–95th percentile); this cannot be ignored. • Non-carcinogenic effects are not expected by acute exposure of PM2.5 (HQ < 1). • The major contributors to PM 2.5 risk were As, Cr(VI), Cd, Mn, BaP, and Pb. • Related sources were industrial activities, combustion of oil, and vehicle exhaust. [ABSTRACT FROM AUTHOR]

Fine particulate matters less than 2.5 µm (PM2.5) in the ambient atmosphere are strongly associated with adverse health effects. However, it is unlikely that all fine particles are equally toxic in view of their different sizes and chemical components. Toxicity of fine particles produced from various combustion sources (diesel engine, gasoline engine, biomass burning (rice straw and pine stem burning), and coal combustion) and non-combustion sources (road dust including sea spray aerosols, ammonium sulfate, ammonium nitrate, and secondary organic aerosols (SOA)), which are known major sources of PM2.5, was determined. Multiple biological and chemical endpoints were integrated for various source-specific aerosols to derive toxicity scores for particles originating from different sources. The highest toxicity score was obtained for diesel engine exhaust particles, followed by gasoline engine exhaust particles, biomass burning particles, coal combustion particles, and road dust, suggesting that traffic plays the most critical role in enhancing the toxic effects of fine particles. The toxicity ranking of fine particles produced from various sources can be used to better understand the adverse health effects caused by different fine particle types in the ambient atmosphere, and to provide practical management of fine particles beyond what can be achieved only using PM mass which is the current regulation standard. [ABSTRACT FROM AUTHOR]