Evaluating the risk of phthalate and non-phthalate plasticizers in dust samples from 100 Japanese houses.

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.

Bis(2-ethylhexyl) phthalate transfer from polyvinyl chloride sheet to several kinds of particles.

Bis(2-ethylhexyl) phthalate (DEHP) transfer from a polyvinyl chloride (PVC) sheet to 9 kinds of particles, namely, polyethylene particles (1-10, 45-53, 90-106 µm), soda lime glass particles (1-38, 45-53, 90-106 µm), black forest soil, carbon black, and cotton linter, for the particle weights of 0.3, 1, 3, and 12 mg/cm2, were determined for 1, 3, 7, and 14 days using a passive flux sampler (PFS), as well as standard dust. Transfer amounts to small polyethylene particles (1-10 µm), black forest soil, and carbon black were large (8.5, 16, and 48 µg/mg-particle, respectively, for 0.3 mg/cm2 for 14 days) and were similar to standard house dust (35 µg/mg-particle). On the other hand, transfer amount to large polyethylene particles (0.056-0.12 µg/mg-particle), soda lime glass (0.18-0.31 µg/mg-particle), and cotton linter (0.42-0.78 µg/mg-particle) were much lower. The DEHP transfer amount to the particles was proportional to the surface area of the particles, but not associated with the organic content. The DEHP transfer amount per surface area to small polyethylene particles was larger than that of other particles, suggesting the contribution of absorption into the polyethylene particle. However, for the larger polyethylene particles with different manufacturing process that may have different crystallinity, the contribution of absorption was small. The amount of DEHP transferred to soda lime glass did not differ from 1 to 14 days, suggesting that an adsorption equilibrium was reached after 1 day. The estimated value of particle/gas partition coefficients of DEHP, Kpg, of small polyethylene, black forest soil and carbon black were much higher (3.6, 7.1, and 18 m3/mg, respectively) than those of large polyethylene and soda lime glass particles (0.028-0.11 m3/mg).

Radiocesium-bearing microparticles discovered on masks worn during indoor cleaning.

A decade has passed since the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident on March 11, 2011. However, radioactive particles have recently been detected in the indoor air of some residences near the FDNPP. Following the recommendations of previous research, we determined the presence of radiocesium-bearing microparticles (CsMPs) and measured the radioactivity of radiocesium that adhered on non-woven face masks worn by six persons during the indoor cleaning of 59 residences in Namie, Futaba, Okuma, and Tomioka towns in Fukushima Prefecture. Of the 284 masks worn in this study, significant 137Cs radioactivity was detected in 268, and 44 new CsMPs were discovered in 28. The results of this study also suggest the presence of highly concentrated soluble radiocesium particles or soluble radioactive cesium aerosols adhered to house dust. This implies that the CsMPs constituted a large proportion of radioactivity in the indoor air contamination for particles in the 1.0-2.5 µm size range due to the radioactive radiocesium particles. It is desirable to wear masks during cleaning to prevent inhalation of CsMPs.

Evaluation of shields and ventilation as a countermeasure to protect bus drivers from infection.

We evaluated the deposition of droplets and droplet nuclei-generated by simulated coughing and talking from three points in a bus-on the driver's face and on surfaces around the driver (e.g., the steering wheel), based on whether countermeasures were taken, and assuming that an infected passenger was talking to the driver. When a shield, such as acrylic boards or polyvinyl chloride (PVC) sheets, was used as the countermeasure, the deposition of artificial droplets (>4 µm), emitted from beside or behind the driver, on his eyes, mouth, and cheeks reduced by two to three orders of magnitude or more. Deposition on the surfaces around the driver was also reduced following the use of shields. For artificial droplet nuclei (1.3 µm of polystyrene latex (PSL)) emitted from atomizers beside the driver, the operation of the ventilation fan (VF) and air conditioner (AC), and defroster (DEF) greatly reduced the driver's exposure, while the use of the shield did not. The infection risk of the driver was estimated through exposure to the virus via transfer to the mucosa via hands or surface-to-finger, direct adhesion on the mucosa, and direct inhalation of droplets and droplet nuclei. This is under the assumption that the droplets and droplet nuclei measured in this study are 40% the diameter of those after immediately leaving the mouth of the infected person and are constant regardless of particle size. When using the shield, total infection risk via droplet, airborne, and contact transmission was decreased by 75.0-99.8%. When the shield was not installed, the infection risk decreased by 9.74-48.7% with the operation of the VF, AC, and/or DEF.

Time-course analysis of pulmonary inflammation induced by intratracheal instillation of nanosized crystalline silica particles in F344 rats.

Crystalline silica is an important cause of serious pulmonary diseases, and its toxic potential is known to be associated with its surface electrical properties. However, in vivo data clarifying the relevance of silica's toxic potential, especially its long-term effects, remain insufficient. To investigate the contribution of physico-chemical property including surface potential on the hazard of nanocrystalline silica, we performed single intratracheal instillation testing using five different crystalline silicas in a rat model and assessed time-course changes in pulmonary inflammation, lung burden, and thoracic lymph node loads. Silica-nanoparticles were prepared from two commercial products (Min-U-Sil5 [MS5] and SIO07PB [SPB]) using three different pretreatments: centrifugation (C), grinding (G), and surface dissolving (D). The five types of silica particles-MS5, MS5_C, SPB_C, SPB_G, and SPB_D-were intratracheally instilled into male F344 rats at doses of 0 mg/kg (purified water), 0.22 mg/kg (SPB), and 0.67, 2, or 6 mg/kg (MS5). Bronchoalveolar lavage, a lung burden analysis, and histopathological examination were performed at 3, 28, and 91 days after instillation. Granuloma formation was present in MS5 group at 91 days after instillation, although granuloma formation was suppressed in MS5_C group, which had a smaller particle size. SPB_C induced severe and progressive inflammation and kinetic lung overload, whereas SPB_G and SPB_D induced only slight and transient acute inflammation. Our results support that in vivo toxic potential of nanosilica by intratracheal instillation may involve with surface electrical properties leading to prolonged effect and may not be dependent not only on surface properties but also on other physico-chemical properties.

Air exchange rates and advection-diffusion of CO2 and aerosols in a route bus for evaluation of infection risk.

As COVID-19 continues to spread, infection risk on public transport is concerning. Air exchange rates (ACH) and advection-diffusion of CO2 and particles were determined in a route bus to evaluate the infection risk. ACH increased with bus speed whether windows were open or closed, and ACH were greater when more windows were open. With two open windows, ACH was greater when a front and rear window were open than when two rear windows were open. With both front and rear ventilation fans set to exhaust, ACH was more than double that when both were set to supply. With air conditioning (AC) off, CO2 and particles spread proportionally at the same rate from a source, whereas with the AC on, the spread rate of particles was about half that of CO2 , because particles might be trapped by a prefilter on the AC unit. Infection risk can be reduced by equipping AC unit with an appropriate filter. Calculations with a modified Wells-Riley equation showed that average infection risk was reduced by 92% in the moving bus with windows open comparing to with windows closed. When the bus was moving with windows closed, exhaust fan operation reduced the average risk by 35%.

Variation in chronic nickel toxicity to Daphnia magna among Japanese river waters and performance evaluation of bioavailability models in predicting the toxicity.

Nickel (Ni) ecotoxicity is dictated by water chemistry characteristics such as pH, water hardness, and amount of dissolved organic carbon. Bioavailability models have been developed to predict Ni toxicity and validated for European, Australian, and US natural waters. In this study, chronic toxicity tests in Ni-spiked Japanese river waters were conducted on a strain of Daphnia magna to test whether the chronic toxicity differs among Japanese natural waters with different water chemistries. Based on the results of chronic Ni toxicity tests, we assessed the performance of existing D. magna bioavailability models, which were developed in artificial waters (Model 1) and calibrated in European natural waters (Model 2), in terms of the accuracy and the bias of model predictions. Furthermore, we also calibrated the two models by using toxicity test results to develop a bioavailability model for Ni chronic toxicity to the strain of D. magna in Japanese river waters. The 10%, 20%, and 50% effect concentrations (EC10, EC20, and EC50) of dissolved Ni on reproduction of the D. magna strain were within ranges from 8.1 to 44.9 µg/L, 9.0 to 57.1 µg/L, and 10.9 to 86.1 µg/L, respectively. Results indicate that differences in water chemistry among Japanese river waters influenced chronic Ni toxicity to the model organism. Model 1predicted 43% of the observed EC10, EC20, and EC50 values within a factor of 2 and 100%, 100%, and 43% within a factor of 3, respectively. Model 2 predicted 14%, 14%, and 29% of the observed EC10, EC20, and EC50 values within a factor of 2 and 43% within a factor of 3. The values of model bias based on the geometric mean of ratios of EC10, EC20 and EC50 values predicted by each of the two models and observed EC10, EC20, and EC50 values were 0.71, 0.65, and 0.62 for Model 1 and 0.27, 0.26, and 0.29 for Model 2, respectively. After calibrating two models using the results of toxicity tests, refined Model 1 predicted 71%, 57%, and 57% of observed EC10, EC20, and EC50 values within a factor of 2 and 100%, 86%, and 100% within a factor of 3; refined Model 2 predicted 71% of observed EC10, EC20, and EC50 values within a factor 2 and 100%, 86%, and 86% within a factor of 3, respectively. Our results indicate that calibrating the Ni bioavailability models in Japanese natural waters increased their predictive capacity by a factor of up to approximately five.

Survey of air exchange rates and evaluation of airborne infection risk of COVID-19 on commuter trains.

To identify potential countermeasures for coronavirus disease (COVID-19), we determined the air exchange rates in stationary and moving train cars under various conditions in July, August, and December 2020 in Japan. When the doors were closed, the air exchange rates in both stationary and moving trains increased with increasing area of window-opening (0.23-0.78/h at 0 m2, windows closed to 2.1-10/h at 2.86 m2, fully open). The air exchange rates were one order of magnitude higher when doors were open than when closed. With doors closed, the air exchange rates were higher when the centralized air conditioning (AC) and crossflow fan systems (fan) were on than when off. The air exchange rates in moving trains increased as train speed increased, from 10/h at 20 km/h to 42/h at 57 km/h. Air exchange rates did not differ significantly between empty cars and those filled with 230 mannequins representing commuters. The air exchange rates were lower during aboveground operation than during underground. Assuming that 30-300 passengers travel in a train car for 7-60 min and that the community infection rate is 0.0050-0.30%, we estimated that commuters' infection risk on trains was reduced by 91-94% when all 12 windows were opened (to a height of 10 cm) and the AC/fan was on compared with that when windows were closed and the AC/fan was off.

Time-course comparison of pulmonary inflammation induced by intratracheal instillation of four different nickel oxide nanoparticles in male Fischer rats.

Occupational exposure to nickel oxide (NiO) is an important cause of respiratory tract cancer. Toxicity is known to be associated with the dissociated component, i.e. nickel (II) ions. To address the relationship between physicochemical properties, including solubility in artificial lysosomal fluid, of NiO and time-course changes in the pulmonary response, we conducted an intratracheal instillation study in male Fischer rats using four different well-characterized NiO products, US3352 (NiO A), NovaWireNi01 (NiO B), I small particle (NiO C), and 637130 (NiO D). The NiOs were suspended in purified water and instilled once intratracheally into male F344 rats (12 weeks old) at 0 (vehicle control), 0.67, 2, and 6 mg/kg body weight. The animals were euthanized on days 3, 28, or 91 after instillation, and blood analysis, bronchoalveolar lavage fluid (BALF) testing, and histopathological examination were performed. The most soluble product, NiO B, caused the most severe systemic toxicity, leading to a high mortality rate, but the response was transient and surviving animals recovered. The second-most-soluble material, NiO D, and the third, NiO A, caused evident pulmonary inflammation, and the responses persisted for at least 91 days with collagen proliferation. In contrast, NiO C induced barely detectable inflammation in the BALF examination, and no marked changes were noted on histopathology. These results indicate that the early phase toxic potential of NiO products, but not the persistence of pulmonary inflammation, is associated with their solubility.

Comparing impacts of metal contamination on macroinvertebrate and fish assemblages in a northern Japanese river.

Researchers have long assessed the ecological impacts of metals in running waters, but few such studies investigated multiple biological groups. Our goals in this study were to assess the ecological impacts of metal contamination on macroinvertebrates and fishes in a northern Japanese river receiving treated mine discharge and to evaluate whether there was any difference between the metrics based on macroinvertebrates and those based on fishes in assessing these impacts. Macroinvertebrate communities and fish populations were little affected at the downstream contaminated sites where concentrations of Cu, Zn, Pb, and Cd were 0.1-1.5 times higher than water-quality criteria established by the U.S. Environmental Protection Agency. We detected a significant reduction in a few macroinvertebrate metrics such as mayfly abundance and the abundance of heptageniid mayflies at the two most upstream contaminated sites with metal concentrations 0.8-3.7 times higher than the water-quality criteria. There were, however, no remarkable effects on the abundance or condition factor of the four dominant fishes, including masu salmon (Oncorhynchus masou). These results suggest that the richness and abundance of macroinvertebrates are more sensitive to metal contamination than abundance and condition factor of fishes in the studied river. Because the sensitivity to metal contamination can depend on the biological metrics used, and fish-based metrics in this study were limited, it would be valuable to accumulate empirical evidence for ecological indicators sensitive to metal contamination within and among biological groups to help in choosing which groups to survey for general environmental impact assessments in metal-contaminated rivers.

Comparison of DNA sequencing and morphological identification techniques to characterize environmental fungal communities.

Culture-independent DNA sequencing of fungal internal transcribed spacer 2 (ITS2) region was compared to a culture-dependent morphological identification technique to characterize house dust-borne fungal communities. The abundant genera were Aspergillus, Wallemia, Cladosporium, and Penicillium. Statistically significant between-method correlations were observed for Wallemia and Cladosporium (Spearman's ρ = 0.75 and 0.72, respectively; p < 0.001). Penicillium tended to be detected with much higher (averaged 26-times) relative abundances by the culture-based method than by the DNA-based method, although statistically significant inter-method correlation was observed with Spearman's ρ = 0.61 (p = 0.002). Large DNA sequencing-based relative abundances observed for Alternaria and Aureobasidium were likely due to multicellularity of their spores with large number of per-spore ITS2 copies. The failure of the culture-based method in detectiing Toxicocladosporium, Verrucocladosporium, and Sterigmatomyces was likely due to their fastidiousness growth on our nutrient medium. Comparing between the two different techniques clarified the causes of biases in identifying environmental fungal communities, which should be amended and/or taken into consideration when the methods are used for future fungal ecological studies.

Resuspension and deposition of PM2.5 and PM10 containing radiocesium during and after indoor cleaning of uninhabited houses in Fukushima, Japan.

Radiocesium contamination in homes could be a serious concern following Japan's 2011 Fukushima Daiichi Nuclear Power Plant accident, including exposure to radiocesium during cleaning when residents return home after the lifting of evacuation orders. This study measured PM2.5 and PM10 concentrations containing radiocesium during cleaning (dusting, vacuuming with a cordless cyclone unit, and vacuuming with a corded paper-pack unit), as well as air exchange rates, in 12 residential houses in Fukushima. Surface dusting of walls, shelves, and furniture significantly increased concentrations of PM2.5 and PM10 by up to 6.3 and 16 times the background (outdoor) level, respectively. Vacuuming with a paper-pack unit increased levels by 2.2 and 3.3 times, while vacuuming with a cordless cyclone unit increased these by 1.3 and 1.5 times, respectively. Measurements in 11 houses revealed an average air exchange rate of 0.22/h and dry deposition rates for PM2.5 and PM10 of 0.13/h and 0.32/h, respectively. Dry deposition rates were not correlated with building age, although the air exchange rates showed statistically significant increases with increasing building age. Dry deposition rates of PM2.5 significantly decreased with increasing air exchange rates.

Estimated internal exposure doses due to indoor radiocaesium contamination in residential houses after the Fukushima nuclear accident.

This work first reports the estimation of the internal exposure from ingestion of house dust and inhalation of aerosol, by employing a measured data on 137Cs activities, bioaccessibility (solubility to water and 1 M HCl), and particle size distribution. The house dust and aerosol samples were collected during the actual indoor cleaning by vacuuming and dusting, from 65 houses and buildings in proximity to the Fukushima Daiichi nuclear power plant (FDNPP) (1.6-16.1 km from the FDNPP) during a period from April 2016 to January 2019. Committed effective doses for an adult owing to the ingestion of house dust of 20 mg per day, which adheres to one's hands through the hand-to-mouth, and those owing to inhalation of aerosol during dusting for 1.5 h while wearing a mask, were calculated using DCAL software for each house or building, as 1.13 µSv and 4.55 µSv as maximum doses, respectively (as of March 2011). Both the committed effective doses, owing to ingestion and inhalation, were inversely correlated with the distance from the FDNPP, and positively correlated with the indoor surface contamination.

Diethylhexyl phthalate (DEHP) emission to indoor air and transfer to house dust from a PVC sheet.

Diethylhexyl phthalate (DEHP) emission to air and transfer to house dust from a polyvinyl chloride (PVC) sheet were quantified for periods of 1, 3, 7, and 14 days using a passive flux sampler (PFS). Japanese Industrial Standards (JIS) test powders class 15 was used as the test house dust in settled weights of 0.3, 1, 3, and 12 mg/cm2. DEHP concentrations in the surface air on the PVC sheet were estimated as 2.6-3.3 µg/m3 according to an emission test without dust. Although DEHP transfer rates from the PVC sheet to the house dust decreased over time, the adsorption did not reach an equilibrium state within 14 days. The transfer rates per dust weight increased with decreasing dust weight on the PVC sheet. The transfer rates per PVC sheet area increased nonlinearly with increasing dust weight on the PVC sheet. DEHP emission from a PVC sheet to air was one to three orders of magnitude lower than DEHP transfer from a PVC sheet to dust. In the case of 0.3 mg/cm2 of settled house dust for 7 days, the emission rates to air were 35, 15, 9.1, 6.4, and 3.8 µg/m2/h for a diffusion distance of 0.90, 1.85, 2.75, 3.80, and 5.75 mm, respectively, and the transfer rate to dust was 5.3 × 102 µg/m2/h (no difference among the five diffusion distances). Compared to residents who clean the floor every day, exposure to DEHP in house dust could be 10 times higher for residents who clean the floor once every two weeks based on the time-weighted average concentrations in house dust.

Does a sum of toxic units exceeding 1 imply adverse impacts on macroinvertebrate assemblages? A field study in a northern Japanese river receiving treated mine discharge.

In ecological risk assessment, sum-of-toxic-unit approaches based on measured water quality factors such as trace metals are used to infer ecological impacts in the environment. However, it is uncertain whether the use of such approaches yields accurate risk predictions. To address this issue, we investigated and compared (1) water quality, including trace metals, and (2) benthic macroinvertebrate communities in a northern Japanese river receiving treated discharge from an abandoned mine and in a nearby reference river. As a sum-of-toxic-unit approach, we employed a cumulative criterion unit (CCU), namely, the sum of the ratios of the dissolved concentrations of a metal (Cu, Zn, Cd, or Pb) divided by the US Environmental Protection Agency hardness-adjusted environmental water quality criterion for that metal. Compared with the reference sites, at the metal-contaminated sites, the richness, abundance, and structure of macroinvertebrate communities were little affected, with CCUs of 1.7 to 7.4, suggesting that CCU values exceeding 1 do not always indicate marked adverse impacts on these metrics. Further study is still required to derive a more compelling conclusion on the generally applicable relationships between CCUs and ecological impacts on river invertebrates. This would lead to better ecological risk assessments based on sum-of-toxic-unit approaches.

Emission characteristics of diethylhexyl phthalate (DEHP) from building materials determined using a passive flux sampler and micro-chamber.

Emission rates of diethylhexyl phthalate (DEHP) from building materials, such as vinyl floorings and wall paper, determined using a passive flux sampler (PFS) were constant over the week-long measurement period. Emission rates for vinyl floorings and wallpaper were linearly correlated to the inverse of diffusion distance, which corresponds to the internal depth of the PFS. Surface-air DEHP concentrations (y0) were estimated as 1.3-2.3 µg/m3 for materials having a boundary layer molecular diffusion rate-limiting step. The partition coefficient (Kmaterial-air) was estimated as 3.3-7.5 × 1010 for these materials. Additionally, emission rates of DEHP from same building materials determined using a micro-chamber were 4.5-6.1 µg/m2/h. Mass transfer coefficients in the micro-chamber (hm) were estimated by comparing the results using the PFS and micro-chamber, and these were 1.1-1.2 × 10-3 and 8.1 × 10-4 m/s for vinyl floorings (smooth surface) and wallpaper (rough surface), respectively. The thickness of boundary layer on the surface of building materials in the micro-chamber were estimated to be 2.5-2.6 and 3.7 mm for vinyl floorings and wallpaper, respectively.

Radiocesium concentration in indoor air during residential house cleaning in Fukushima Dai-ichi nuclear power plant evacuation areas.

After the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident, outdoor decontamination was conducted by the Japanese Government, whereas indoor contamination was the responsibility of individual residents. However, no data exist regarding 137Cs exposure during indoor cleaning. Therefore, indoor 137Cs radioactivity concentrations in indoor air were determined during cleaning in 60 houses within the evacuation area near the FDNPP, Fukushima Prefecture, Japan. Radiocesium activity concentrations per cubic meter of indoor air during dusting (mean ±â€¯SD (median)) was 6.8 ±â€¯7.9 (4.7) and 1.6 ±â€¯2.7 (0.78) Bq/m3 for all aerodynamic diameter of aerosol particle and PM2.5, respectively. Radiocesium activity concentrations in indoor air decreased with decreasing the aerodynamic diameter of aerosol particles (mean: 0.099, 0.22, 0.41, 0.92, 2.2, and 2.9 Bq/m3 for the aerodynamic diameter of <0.25, 0.25-0.5, 0.5-1.0, 1.0-2.5, 2.5-6.6, and >6.6 µm, respectively) and was inversely proportional to the square of the distance from the FDNPP. Indoor 137Cs radioactivity concentrations were significantly higher during dusting than during vacuuming with either a cyclone handy cleaner or a normal vacuum cleaner. The mean deposited activities in tracheobronchial and alveolar regions was estimated to be 1.9 and 2.8 Bq, respectively, during a 2-h dusting period in the studied houses. For values below the detection limit, half of the detection limit was used for calculating the means and SDs.

Radiocesium contamination in house dust within evacuation areas close to the Fukushima Daiichi nuclear power plant.

Outdoor decontamination efforts have been ongoing since the Fukushima Daiichi nuclear power plant (FDNPP) accident; however, little is known about indoor contamination. Therefore, house dust was sampled based on particle size in 21 wooden buildings (19 residential houses and 2 community centers) within the evacuation area close to the FDNPP, Fukushima Prefecture, Japan. Activities of radiocesium (137Cs) per gram of house dust increased with decreasing particle size (mean: 6.1 × 103, 2.6 × 103, 1.6 × 103, 7.5 × 102, 5.0 × 102, and 4.6 × 102 Bq/g for <4-20, 20-63, 63-180, 180-500, 500-1000, and 1000-2000 µm, respectively). The 137Cs concentrations in house dust were inversely related to the square of distance from the FDNPP for <4-1000 µm particles. From the results of the multiple linear regression analysis, distance from the FDNPP and direction from the FDNPP (northwest) were significantly related to the radioactivity of house dust. It was found that 19%, 33%, and 48% of 137Cs in house dust were extracted in water, 1 M HCl, and not extracted, respectively. Considering the bioaccessibility and assuming a 20 mg/day daily intake of house dust, the daily doses would be 7.2 Bq/day (mean) and 18 Bq/day (95th percent quantile). These results provide valuable insight into indoor radioactive Cs contamination in the area around the FDNPP and possible oral exposure to indoor radioactive Cs after returning home.

Kinetics and dissolution of intratracheally administered nickel oxide nanomaterials in rats.

BACKGROUND: The toxicokinetics of nanomaterials are an important factor in toxicity, which may be affected by slow clearance and/or distribution in the body. METHODS: Four types of nickel oxide (NiO) nanoparticles were single-administered intratracheally to male F344 rats at three doses of 0.67-6.0 mg/kg body weight. The rats were sacrificed under anesthesia and the lung, thoracic lymph nodes, bronchoalveolar lavage fluid, liver, and other organs were sampled for Ni burden measurement 3, 28, and 91 days post-administration; Ni excretion was measured 6 and 24 h after administration. Solubility of NiO nanoparticles was determined using artificial lysosomal fluid, artificial interstitial fluid, hydrogen peroxide solution, pure water, and saline. In addition, macrophage migration to trachea and phagosome-lysosome-fusion rate constants were estimated using pulmonary clearance and dissolution rate constants. RESULTS: The wire-like NiO nanoparticles were 100% dissolved by 24 h when mixed with artificial lysosomal fluid (dissolution rate coefficient: 0.18/h); spherical NiO nanoparticles were 12% and 35% dissolved after 216 h when mixed with artificial lysosomal fluid (1.4 × 10-3 and 4.9 × 10-3/h). The largest irregular-shaped NiO nanoparticles hardly dissolved in any solution, including artificial lysosomal fluid (7.8 × 10-5/h). Pulmonary clearance rate constants, estimated using a one-compartment model, were much higher for the NiO nanoparticles with a wire-shape (0.069-0.078/day) than for the spherical and irregular-shaped NiO nanoparticles (0-0.012/day). Pulmonary clearance rate constants of the largest irregular-shaped NiO nanoparticles showed an inverse correlation with dose. Translocation of NiO from the lungs to the thoracic lymph nodes increased in a time- and dose-dependent manner for three spherical and irregular-shaped NiO nanoparticles, but not for the wire-like NiO nanoparticles. Thirty-five percent of the wire-like NiO nanoparticles were excreted in the first 24 h after administration; excretion was 0.33-3.6% in that time frame for the spherical and irregular-shaped NiO nanoparticles. CONCLUSION: These findings suggest that nanomaterial solubility differences can result in variations in their pulmonary clearance. Nanoparticles with moderate lysosomal solubility may induce persistent pulmonary inflammation.

Discovery of non-spherical heterogeneous radiocesium-bearing particles not derived from Unit 1 of the Fukushima Dai-ichi Nuclear Power Plant, in residences five years after the accident.

Non-spherical heterogeneous radiocesium-bearing particles were found on masks worn during cleaning work in residences near the Fukushima Dai-ichi Nuclear Power Plant (FDNPP), from which residents had evacuated. Three slightly larger (6.6-12 µm) non-spherical radiocesium-bearing particles were found in a residence in Futaba Town, a straight distance of 2.11 km west-northwest from the FDNPP. These were collected on October 25, 2016, 5 years and 7 months after the Fukushima Dai-ichi nuclear disaster and were presumed to originate from the Plant's Unit 2 based on the measured radioactivity ratio of 134Cs/137Cs. The main elemental composition was similar to particles already reported in other studies. However, this is the first time that such particles had a clearly heterogeneous distribution.