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This study aimed to determine the effectiveness of triamcinolone acetonide in suppressing inflammation after blepharoptosis surgery. The study was designed as prospective, randomized, two medical centers' clinical trial. Thirty-two patients with involutional blepharoptosis of the same degree in both eyelids underwent bilateral transcutaneous levator advancement. At the end of the surgery, 4 mg/0.1 ml of triamcinolone acetonide was injected into a randomly selected upper eyelid. The fellow eyelid was not injected and was used as control. Facial photographs were taken on day 1, week 1, month 1, and month 3, and the degree of inflammation, the margin reflex distance 1 (MRD-1), and levator function (LF) between the two eyelids of each patient were compared. The primary outcome was the selection of the less inflamed eyelid decided by the majority of three individuals unrelated to the study. MRD-1 and LF were analyzed for secondary outcomes. As a result, the injected eyelid was judged to be the less inflamed eyelid in all cases. The MRD-1 in the postoperative period less than 1 month was significantly larger in the injected eyelids than the control eyelids (P <0.03). The postsurgical MRD-1 at month 3, the postsurgical LF at all postsurgical examination times were not statistically different. Adverse complications by the injection, including ptosis, levator dysfunction, increase of the intraocular pressure, and visual disturbance were not observed. In conclusion, a triamcinolone acetonide injection after ptosis surgery is both safe and effective in reducing the early postsurgical inflammation and helpful in an earlier return to a daily routine for the patients. [ABSTRACT FROM AUTHOR]

Adverse health effects of heavy metals are a public health concern, especially lead may cause negative health impacts to human fetal and infantile development. The lead concentrations in Pakistani pregnant women's nails, used as a biomarker, were measured to estimate the lead exposure. Thirteen nail samples out of 84 nails analyzed contained lead higher than the concentration (13.6 μg/g) of the fatal lead poisoning case, raising the possibility of an external contamination. Eye cosmetics such as surma are recognized as one of the important sources of lead exposure in Pakistan. We collected in Pakistan 30 eye cosmetics made in Pakistan, Saudi Arabia and western countries. As the metal composition analysis by energy dispersive X-ray fluorescence spectrometry revealed that some surma samples contained lead more than 96%, the surma might contaminate the nail specimen. Scanning electron microscopy observations showed that lead-containing surma consists of fine particle of galena (ore of lead sulfide) in respirable dust range (less than 10 μm). In addition, relative in vitro bioavailability of lead in the surma was determined as 5.2%. Thus, lead-containing surma consists of inhalable and bioavailable particles, and it contributes an increased risk of lead exposure. Moreover, the relationship between the surma and the lead-contaminated nails by lead isotope ratios analysis indicated the potential of lead contamination in nails by surma. These results suggest that lead in the nails was derived both from body burden of lead and external contamination by lead-containing surma. Therefore, nail is not suited as a biomarker for lead exposure in the countries where surma used, because we may overestimate lead exposure by surface lead contamination in the nail by surma. [ABSTRACT FROM AUTHOR]

The levels of 25 elements in house dust collected from 100 general Japanese residences were measured. Factor analysis was applied on the multi-element data to explore source of Pb (median concentration 49.1 mg/kg) in house dust. Six factors were extracted and Pb was found to have great loading on the fifth factor with Sb and Sn, suggesting solder (Sn), and plastic and metals (Sb) may be the sources of Pb in the house dust of Japanese residences. No significant loading was found on soil-related factors indicating non-significant contribution of Pb in track-in soil. Seven heavy metals (Cd, Cu, Mo, Pb, Sb, Sn, and Zn) were found in house dust at >10 times more condensed than crustal abundance. Health risk of these elements to children via the ingestion of house dust was estimated based on the comparison with tolerable daily intake and found to be non-significant for most of the elements. [Copyright &y& Elsevier]

The Fukushima Dai-ichi Nuclear Power Plant accidents following the March 11, 2011 Tohoku earthquake, and subsequent tsunami released radioactive materials into the atmosphere and caused significant public health concerns, particularly thyroid cancers in children. However, the lack of measurement data for atmospheric concentrations of 131I has caused persistent and widespread uncertainty. This study estimated the maximum potential thyroid doses of inhaled 131I in the early post-accident phase between March 12 and 23, 2011 by using the hourly measured data of the 137Cs concentrations at 101 suspended particulate matter (SPM) monitoring sites, a new multi-model ensemble (MME) method of simulating 137Cs concentrations using two Atmospheric Transport and Deposition Models (ATDMs), the 131I/137Cs ratio obtained from measurement data analysis, and the internal exposure model. Based on the measurements, the maximum potential thyroid doses were estimated at 3.1–160 mSv at 5 sites in the Fukushima-Hamadori area for 1-year-old children assumed to remain outdoors, whereas they were less than 4.3 mSv at the other sites in the base case of the 131I/137Cs ratio. The spatial distribution of the maximum potential of early inhalation doses was estimated by using the MME and measurements. The inhalation thyroid doses in the evacuation scenarios were compared to the estimates reported by previous studies. The results of the present study were almost congruent with the outcomes of previous investigations except for thyroid doses contributed by highly contaminated plumes on March 12 and 15. The sensitivity analysis for the 131I/137Cs ratio indicated that these plumes carried the potential to significantly increase the thyroid doses of residents. • Early thyroid doses from inhaled 131I after the FDNPP accident were estimated. • Multi-ensemble ATDM and hourly measured 137Cs data could improve the estimation. • Plumes on March 12 and 15, 2011 had potential to change the previous estimations. [ABSTRACT FROM AUTHOR]

The radiation dose effects due to the Fukushima Daiichi Nuclear Power Plant (FDNPP) accident are of public concern. Although indoor dust is an important exposure route for some hazardous chemicals, the radiation exposure dose from the radioactive caesium (Cs) in it has not been well investigated. Hence, in this study, we measured the radioactive Cs in the indoor dust of private houses in order to estimate the resulting human exposure. We collected vacuum cleaner dust twice (in April and June 2012, n = 250 and 241, respectively) in the prefectures of Chiba and Ibaraki, from houses located 150–200 km south from the FDNPP. The activity concentrations of 134Cs and 137Cs in the indoor dust were measured using germanium γ-ray detectors, and the exposure dose was calculated and the household-to-household variations were analysed. The median activity concentrations of 134Cs + 137Cs in the indoor dust collected in April and June were 1470 and 1340 Bq kg−1, respectively. The median committed effective doses via indoor dust ingestion were estimated as 0.73, 0.66, and 0.43 × 10−3 mSv year−1, and those via inhalation were estimated as 0.03, 0.04, and 0.06 × 10−3 mSv year−1 for one- and ten-year-old children and adults, respectively. Those were much smaller than the annual dose limit of 1 mSv year−1, which was set as a goal to be achieved in the a few years or decades (clear period has not been set). Within the detached houses, multiple regression analysis showed that wet wiping of floor was a significant reduction factor of the Cs concentration in dust; however, the small determination coefficient implies the presence of factors that were not considered in this study. • Radioactive Cs in indoor dust (vacuum cleaner dust) from houses located 150–200 km south from the FDNPP was measured. • The median committed effective dose via indoor dust ingestion and indoor air inhalation was less than 1 × 10-3 mSv year-1. • Wet wiping of indoor floor was a significant reduction factor of the radioactive Cs concentration in indoor dust. [ABSTRACT FROM AUTHOR]

Phthalates are widely used as plasticizer and associated with various health issues. Recently, non-phthalate plasticizers are replacing phthalates; however, the exposure to these substances and the risk in Japan is unclear. In this study, we assessed the concentrations of phthalates, non-phthalate plasticizers, and phthalate degradation products in house dust and determined their respective exposure risks via oral and dermal routes. Twelve phthalates, seven non-phthalate plasticizers, and two degradation products were determined in the house dust obtained from 100 Japanese homes. The median concentration of di(2-ethylhexyl) phthalate (DEHP), accounting for 85 % of the total concentration of phthalates and non-phthalate plasticizers detected in this study, was 2.1 × 103 μg/g of dust. Apart from DEHP, diisononyl phthalate (DINP) and di(2-ethylhexyl) terephthalate (DEHT) were the most abundant in the house dust, accounting for 6.2 % (median: 1.7 × 102 μg/g of dust) and 6.1 % (median: 1.7 × 102 μg/g of dust) of the total concentrations, respectively. DEHP and DEHT concentrations in house dust were higher in apartment and small houses (floor area: ≤30 m2 or 31–60 m2 for DEHP and 31–60 m2 for DEHT) than in detached and large houses (floor area: ≥121 m2). Conversely, di-n-butyl phthalate (DnBP) concentrations were significantly higher in detached and large houses (floor area: ≥121 m2) than in apartment and small houses (floor area: ≤30 m2). The total hazard quotient (HQ), using the maximum concentration in house dust, revealed that oral and dermal exposure to house dust was 1.3 × 10-6–0.11 for adults (all substances) and 1.6 × 10-5–2.2 × 10-2 for preschool children (except for DnBP and DEHP), suggesting no risk. The HQs for DnBP and DEHP exposure via house dust for preschool children using the maximum values were 0.46 and 1.2, and 6.0 × 10-3 and 0.18 using the median values, indicating that risk of DEHP exposure should be exhaustively determined by considering other exposure routes that were not evaluated in this study, such as diet. [ABSTRACT FROM AUTHOR]

In order to obtain information on thermochemical reactions of chlorophenols, which are well known as dioxin precursors, occurring during the combustion of municipal solid wastes, the combustion of 2,4,6-trichlorophenol (2,4,6-T3CP) in an air stream was investigated over a temperature range of 500¿800°C for a residence time of 1¿20s using a quartz flow reactor. Gas chromatographic/mass spectrometric (GC/MS) analysis of the gaseous products and residues showed that 2,4,6-T3CP began to decompose at 500°C and produced several compounds, with 1,3,6,8- and 1,3,7,9-tetrachlorodibenzo-p-dioxins (T4CDD) as the major products. In addition, more than fifty organic products were observed in our experimental conditions. The yields of polychlorinated benzenes, phenols, dibenzofurans, and dibenzo-p-dioxins formed during the combustion of 2,4,6-T3CP were plotted as a function of temperature and residence time. Furthermore, it was found that the yields and the compositions of these gaseous products were strongly dependent on the residence time in the flow reactor. [Copyright &y& Elsevier]

Environmental phenols are widely distributed in the environment and human samples, suggesting potential exposure to these chemicals. We designed an intervention trial with 30 participants over 6 days to assess the urinary concentrations and half-lives of environmental phenols in Japanese young people. The target environmental phenols include three parabens (methyl paraben, ethyl paraben, and propyl paraben), two benzophenones (benzophenone 1 and 3), two bisphenols (bisphenol F and bisphenol S), and triclosan. Throughout the intervention, the participants consumed the same food and drinks and used personal care products provided by the project. The target phenols were measured in urine from the participants using a liquid chromatography-tandem mass spectrometer. We compared the measured concentrations between the study periods to better understand the exposure tendency. Some statistically significant differences were observed. All target analytes were detected in more than 50% of samples collected on Day 0 (the day before the intervention). Methyl paraben was the dominant phenol detected in urine (1640 μg/g-creatinine), followed by ethyl paraben (119 μg/g-creatinine). Downward trends in creatinine-corrected concentrations were observed for all target analytes in some instances. Non-compartment analysis was performed to estimate urinary excretion parameters. The estimated half-lives ranged from 7.69 to 20.3 h. Use of paraben-free products during the intervention period reduced the body burden. [Display omitted] • Intervention trial with controlled diet and personal care products was conducted. • Urinary parabens, bisphenols, benzophenones and triclosan were measured for 7 days. • Parabens, especially methyl paraben, were dominant phenols detected in urine. • Significant differences were observed between preintervention and intervention. • The estimated elimination half-lives ranged from 7.69 (PrP) – 20.3 (BPF) hours. [ABSTRACT FROM AUTHOR]

Abstract: This study was conducted to investigate the agonistic activity against human retinoic acid receptor (RAR) α in the Lake Biwa–Yodo River and the Ina River in the Kinki region of Japan. To accomplish this, a yeast two-hybrid assay was used to elucidate the spatial and temporal variations and potential sources of RARα agonist contamination in the river basins. RARα agonistic activity was commonly detected in the surface water samples collected along two rivers at different periods, with maximum all-trans retinoic acid (atRA) equivalents of 47.6ng-atRA/L and 23.5ng-atRA/L being observed in Lake Biwa–Yodo River and Ina River, respectively. The results indicated that RARα agonists are always present and widespread in the rivers. Comparative investigation of RARα and estrogen receptor α agonistic activities at 20 stations along each river revealed that the spatial variation pattern of RARα agonist contamination was entirely different from that of the estrogenic compound contamination. This suggests that the effluent from municipal wastewater treatment plants, a primary source of estrogenic compounds, seemed not to be the cause of RARα agonist contamination in the rivers. Fractionation using high performance liquid chromatography (HPLC) directed by the bioassay found two bioactive fractions from river water samples, suggesting the presence of at least two RARα agonists in the rivers. Although a trial conducted to identify RARα agonists in the major bioactive fraction was not completed as part of this study, comparison of retention times in HPLC analysis and quantification with liquid chromatography–mass spectrometry analysis revealed that the major causative contaminants responsible for the RARα agonistic activity were not RAs (natural RAR ligands) and 4-oxo-RAs, while 4-oxo-RAs were identified as the major RAR agonists in sewage in Beijing, China. These findings suggest that there are unknown RARα agonists with high activity in the rivers. [Copyright &y& Elsevier]

Numerous poly- and perfluoroalkyl substances (PFAS) have been manufactured and distributed on the world market. Research on PFAS has highlighted their global distribution and impacts on ecosystems and human health. Following regulations and public concern, PFAS production has shifted toward novel molecules in recent years. New classes of PFAS have been identified in the environment and are gaining worldwide attention. The development of an efficient strategy for identification and quantification of emerging PFAS is essential for risk assessment. This review presents and discusses the most recent analytical method development for PFAS in air, water, abiotic solid matrices and biological matrices, and addresses non-target approaches. Various methods are covered including sampling, pre-treatment (enrichment, extraction and clean-up) and instrumental analysis, and their applications, advantages, shortcomings and future needs are explored. • We discuss recent trends in analytical methods for PFAS in various matrices. • PFAS in air, water, abiotic solids and biological samples are investigated. • Our review covers various methods including sampling, pretreatment and measurement. • We review current analytical techniques and their performance to help future PFAS research. [ABSTRACT FROM AUTHOR]