Preparation of fragmented polyethylene nanoplastics using a focused ultrasonic system and assessment of their cytotoxic effects on human cells.

With the growing prevalence of plastic use, the environmental release of plastic waste is escalating, and fragmented nanoscale plastic particles are emerging as significant environmental threats. This study aimed to evaluate the cytotoxic effects of fragmented polyethylene nanoplastics (PE NPs) manufactured using a focused ultrasonic system. The ultrasonic irradiation process generated fragmented PE NPs with a geometric mean diameter of 85.14 ± 5.37 nm and a size range of 25-350 nm. To assess cytotoxicity, we conducted a series of tests on various human cell lines, including stomach, blood, colon, lung, skin, liver, and brain-derived cells. The testing involved MTS-based cell viability assays to evaluate direct impacts on cell viability, lactate dehydrogenase (LDH) leakage assays to measure membrane damage, and ELISA to quantify TNF-α release as an indicator of inflammation. Although PE-NPs did not immediately induce apoptosis, significant LDH leakage and elevated TNF-α levels were observed across all cell lines, indicating membrane damage and inflammatory responses. Additionally, flow cytometry and TEM analyses revealed the intracellular accumulation of PE-NPs, further supporting their cytotoxic potential. These results demonstrate that fragmented PE-NPs can disrupt cellular membranes and induce inflammatory responses through accumulation within cells. The findings suggest that these NPs pose potential hazards to cell viability and underscore the need for further research into their environmental and health impacts.

Fluorescence microfluidic system for real-time monitoring of PS and PVC sub-micron microplastics under flowing conditions.

Plastics, recognized for their convenience, disposability, and recyclability, have emerged as a significant ecological challenge, particularly with the prevalence of microplastics (MPs, 1 µm - 5 mm) and sub-micron MPs (100 - 1000 nm) in natural environments. While extensive research has focused on their occurrence and environmental impacts, quantification methods developed for MPs exhibit limitations when applied to sub-micron MPs due to their smaller size. This study addresses these limitations by introducing a novel monitoring system that integrates fluorescence labeling with a microfluidic device and particle tracking software, enabling automated quantification and size measurement of both spherical and fragmented MPs of size in the sub-micrometer range. Results showed that the developed system enabled fast quantification and size measurement of 500- and 1000-nm polystyrene (PS) sub-micron MP beads and fragmented PS and polyvinyl chloride (PVC) sub-micron MPs. Additionally, fluorescence labeling enabled the real-time discrimination of PS and PVC sub-micron MPs. Lastly, the microfluidic system allowed the monitoring of sub-micron MPs within a small quantity of water samples. This automated system has a high potential for swift and real-time monitoring of sub-micron MPs in the environment. By enhancing our ability to detect and quantify sub-micron MPs, this study contributes to a more comprehensive understanding of their presence and distribution in environmental systems.

Analysis of micro(nano)plastics based on automated data interpretation and modeling: A review.

The widespread presence of micro(nano)plastics (MNPs) in the environment threatens ecosystem integrity, and thus, it is necessary to determine and assess the occurrence, characteristics, and transport of MNPs between ecological components. However, most analytical approaches are cost- and time-inefficient in providing quantitative information with sufficient detail, and interpreting results can be difficult. Alternative analyses integrating novel measurements by imaging or proximal sensing with signal processing and machine learning may supplement these approaches. In this review, we examined published research on methods used for the automated data interpretation of MNPs found in the environment or those artificially prepared by fragmenting bulk plastics. We critically reviewed the primary areas of the integrated analytical process, which include sampling, data acquisition, processing, and modeling, applied in identifying, classifying, and quantifying MNPs in soil, sediment, water, and biological samples. We also provide a comprehensive discussion regarding model uncertainties related to estimating MNPs in the environment. In the future, the development of routinely applicable and efficient methods is expected to significantly contribute to the successful establishment of automated MNP monitoring systems.

Effects of different sizes of polystyrene micro(nano)plastics on soil microbial communities.

Micro(nano)plastic (MNP) pollution in soil environments is a major concern, but the effects of different sizes of MNPs on soil microbial communities, which are crucial in nutrient cycling, has not been well investigated. In this study, we aimed to determine the effects of polystyrene (PS) MNPs of different sizes (0.05-, 0.5-, and 5-µm) on soil microbial activity and community composition. Changes in inorganic N concentration, microbial biomass, and extracellular enzyme activities were determined in soils treated with 100 and 1000 µg PS MNPs g-1 soil during a 40-d incubation experiment. Soil microbial biomass was significantly lowered when soils were treated with 0.5- or 5-µm MNPs at 100 and 1000 µg PS MNPs g-1 soil. NH4+ concentration was higher in soils treated with 5-µm MNPs at 100 and 1000 µg g-1 soil than in the control soils at day 1, suggesting that MNPs inhibited the soil nitrification in short term. In contrast, extracellular enzyme activity was not altered by MNPs. The composition of microbial communities analyzed by Illumina MiSeq sequencing changed; particularly, the relative abundance of several bacteria related to N cycling, such as the genus Rhizomicrobium belonging to Alphaproteobacteria was decreased by 0.5- and 5-µm MNPs. Our study shows that the size of MNPs is an important factor that can determine their effects on soil microbial communities. Therefore, the size effects need to be considered in assessing the environmental impacts of MNPs.

Parametric studies during the removal of ammonia by membrane contactor with various stripping solutions.

Although membrane contactors (MCs) have been recognized to be an efficient approach for the removal of ammonia from water streams, factors affecting the MCs performance were not clearly investigated. In this study, the effects of stripping solution chemistry (acid types and concentration), feed solution chemistry (pH, temperature, and ammonia concentration), and stages of MCs system have been comprehensively evaluated. Interestingly, the type of stripping solutions significantly affected the removal of ammonia, and the comparative effectiveness were in the order of H3PO4 > H2SO4 > HCOOH. However, the concentration of stripping solutions and ammonia in the feed has little impact to the performance of MCs. Among the feed solution chemistry, pH and temperature were the most crucial factors for ammonia removal in MCs, because the increase of pH and temperature enhanced the free ammonia fraction in the solution and facilitated the mass transfer through pores. At the absorbent concentration of 0.5 M H3PO4, pH of 10, and temperature of 40 °C, single-stage MCs could achieve 51% of ammonia removal within 40 s, and the ammonia removal rate in two-stage MCs reached 90% at the 1.5 min of hydraulic retention time (HRT). The results suggested the superior feasibility of multi-stage MCs system compare to the conventional stripping processes for the removal of ammonia in various waste or wastewater.

Application of colorimetric sensor in monitoring dissolved CO2 in natural waters.

Dissolved CO2 originating from underground structures at high concentrations may pose a threat to public and environmental health. Therefore, a convenient monitoring technique that allows fast detection of dissolved CO2 needs to be developed. In this study, a low-cost colorimetric CO2 sensor was applied for monitoring dissolved CO2. The sensor is composed of an acrylic reactor, cresol red pH indicator solution, and a gas-permeable membrane, and the performance of the sensor was tested for the detection of dissolved CO2 at the range of 2-800 mg CO2 L-1. Color change of the detection solution within the sensor was mainly dependent on CO2 dissolved in the water sample. This was analyzed using an RGB program that extracts the red, green, and blue intensity of a target color on a scale of 0-255. ΔGB, an index of CO2 concentration corresponding to the change in intensity of green (G) and blue (B) extracted by the RGB program, exhibited a linear relationship with dissolved CO2 concentrations (r2 > 0.95, p < 0.005). In the field, the sensor was able to measure dissolved CO2 between 10 and 411 mg CO2 L-1 within 1 min. Overall, our CO2 sensor has high potential to be used in detection of dissolved CO2 in groundwater and surface waters.

Compensatory Protection of Thioredoxin-Deficient Cells from Etoposide-Induced Cell Death by Selenoprotein W via Interaction with 14-3-3.

Selenoprotein W (SELENOW) is a 9.6 kDa protein containing selenocysteine (Sec, U) in a conserved Cys-X-X-Sec (CXXU) motif. Previously, we reported that SELENOW regulates various cellular processes by interacting with 14-3-3ß at the U of the CXXU motif. Thioredoxin (Trx) is a small protein that plays a key role in the cellular redox regulatory system. The CXXC motif of Trx is critical for redox regulation. Recently, an interaction between Trx1 and 14-3-3 has been predicted. However, the binding mechanism and its biological effects remain unknown. In this study, we found that Trx1 interacted with 14-3-3ß at the Cys32 residue in the CXXC motif, and SELENOW and Trx1 were bound at Cys191 residue of 14-3-3ß. In vitro binding assays showed that SELENOW and Trx1 competed for interaction with 14-3-3ß. Compared to control cells, Trx1-deficient cells and SELENOW-deficient cells showed increased levels of both the subG1 population and poly (ADP-ribose) polymerase (PARP) cleavage by etoposide treatment. Moreover, Akt phosphorylation of Ser473 was reduced in Trx1-deficient cells and was recovered by overexpression of SELENOW. These results indicate that SELENOW can protect Trx1-deficient cells from etoposide-induced cell death through its interaction with 14-3-3ß.

Highly efficient colorimetric CO2 sensors for monitoring CO2 leakage from carbon capture and storage sites.

Carbon capture and storage (CCS) technology used for reducing anthropogenic CO2 emissions involves the capture of CO2 from industrial sources and its injection into geological sinks, such as oil reservoirs and abandoned gas fields. To ensure environmental and public safety in implementing CCS technology, efficient CO2-monitoring technology must be developed to detect potential CO2 leakage from CCS sites. Conventional CO2 sensors used for monitoring CCS sites are typically high in cost and require professional staff for maintenance. In this study, we developed a portable and low-cost colorimetric CO2 sensor with high soil CO2 detection efficiency for CCS sites. The sensor consists of a detection solution that contains the pH indicator cresol red encapsulated with a gas-permeable membrane. When CO2 enters the sensor through the membrane, the color of the pH indicator changes and this was quantified using an RGB (red, green, blue) application (app), an app that measures the RGB values of a given color. The change in G and B values of the detection solution showed a significant linear relationship with soil CO2 concentration determined via non-dispersive infra-red (NDIR) CO2 sensor (r2 = 0.98, p = 0.001), and thus these values were used for quantification of CO2 concentration. Tests using CO2-injection chamber showed that the optical CO2 sensors can detect soil CO2 concentration of 0.1 to 30% within a few minutes. Field studies conducted at a natural CO2 vent and an artificial CO2 leakage site showed that the optical CO2 sensors can be applied in analyzing surficial CO2 leakage patterns. The advantage of this optical CO2 sensor when applied to field monitoring is that it is inexpensive and has few installation restrictions. Therefore, this optical CO2 sensor has a strong potential for use in monitoring CO2 leakages from CCS sites.

Effects of graphene oxides and silver-graphene oxides on aquatic microbial activity.

Graphene oxide (GO) and silver-graphene oxide (Ag-GO) are used in various fields, such as biotechnology and environmental engineering, due to their unique material properties, including hydrophilicity, high surface area, mechanical strength, and antibacterial activity. With the increase in the usage of such nanomaterials, they are likely to enter the aquatic environment during the manufacturing process, product use, and disposal. However, the effects of GO and Ag-GO on aquatic microbial activities are not well understood. In this study, we aimed to determine the effects of GO and Ag-GO on the aquatic microbial communities inhabiting a river and a lake located in Seoul, South Korea. Unfiltered natural surface water samples were exposed to GO and Ag-GO at a final concentration of 10 to 100 mg L-1 for 48 h. The activity of leucine aminopeptidase was significantly lowered within 1 h of GO and Ag-GO treatments and nitrification rate was significantly lowered. An increase in intracellular lactate dehydrogenase levels of up to 5% was observed in natural waters under GO and Ag-GO treatments compared to the control (0%), indicating cell membrane damage. In addition, generation of intracellular reactive oxygen species increased up to 184% under 100 mg GO L-1 and 102% under 100 mg Ag-GO L-1 treatment compared to the control (0%). Our results indicate that the activities of microorganisms inhabiting natural surface waters may have been inhibited by oxidative stress and cell membrane damage induced by GO and Ag-GO. We believe that our results may contribute to the development of regulatory guidelines on the release of emerging engineered nanomaterials to the environment.

Effects of silver-graphene oxide nanocomposites on soil microbial communities.

Due to the application of silver-graphene oxide (Ag-GO) in diverse fields, it is important to investigate its potential impacts on the environment including soils. In this study, the response of microbial communities in soils treated with Ag-GO synthesized by glucose reduction was determined by analyzing enzyme activities, biomass, and inorganic N concentrations and by pyrosequencing. In soils treated with 0.1-1 mg Ag-GO g-1 soil, the activities of ß-glucosidase, cellobiohydrolase, and xylosidase decreased up to 80% and NO3- concentration decreased up to 82% indicating inhibited nitrification. Within the bacterial community, the relative abundance of Acidobacteria and Cyanobacteria in soils treated with Ag-GO were lower than that in control soil. Meanwhile, the relative abundance of AD3 and Firmicutes tended to increase under Ag-GO treatments. These changes in bacterial community composition reflected lowered activities associated with C and N cycling. On the other hand, microbial biomass showed no distinct change in response to Ag-GO treatment. Our study can serve as important basis in establishing guidelines for regulating the release of nanocomposites such as Ag-GO to the soil environment.

Effects of graphene oxides on soil enzyme activity and microbial biomass.

Due to recent developments in nanotechnology, nanomaterials (NMs) such as graphene oxide (GO) may enter the soil environment with mostly unknown consequences. We investigated the effects of GO on soil microbial activity in a 59-day soil incubation study. For this, high-purity GO was prepared and characterized. Soils were treated with up to 1 mg GO g(-1) soil, and the changes in the activities of 1,4-ß-glucosidase, cellobiohydrolase, xylosidase, 1,4-ß-N-acetyl glucosaminidase, and phosphatase and microbial biomass were determined. 0.5-1 mg GO g(-1) soil lowered the activity of xylosidase, 1,4-ß-N-acetyl glucosaminidase, and phosphatase by up to 50% when compared to that in the control soils up to 21 days of incubation. Microbial biomass in soils treated with GO was not significantly different from that in control soils throughout the incubation period, and the soil enzyme activity and microbial biomass were not significantly correlated in this study. Our results indicate that soil enzyme activity can be lowered by the entry of GO into soils in short term but it can be recovered afterwards.