Acellular assays of oxidative potential (OP) induced by ambient particulate matters (PMs) are of great significance in screening for toxicity in PMs. In this review, several typical OP measurement techniques, including the respiratory tract lining fluid assay (RTLF), ascorbate depletion assay (AA), dithiothreitol assay (DTT), chemiluminescent reductive acridinium triggering (CRAT), dichlorofluorescin assay (DCFH) and electron paramagnetic/spin resonance assay (EPR/ESR) are discussed and their sensitivity to different PMs species composition, PMs size distribution and seasonality is compared. By comparison, the DTT assay tends to be the preferred method providing a more comprehensive measurement with transition metals and quinones accumulated in the fine PMs fraction. Specific transition metals (i.e., Mn, Cu, Fe) and quinones are found to contribute OP^DTT directly whereas the redox properties of PMs species may be changed by the interactions between themselves. The selection of the appropriate OP measurement methods and the accurate analysis of the relationship between the methods and PM components is conducive to epidemiological researches which are related with oxidative stress induced by PMs exposure.

Nanoplastics (NPs) are a rapidly developing subject that is relevant in environmental and food research, as well as in human toxicity, among other fields. NPs have recently been recognized as one of the least studied types of marine litter, but potentially one of the most hazardous. Several studies are now being reported on NPs in the environment including surface water and coast, snow, soil and in personal care products. However, the extent of contamination remains largely unknown due to fundamental challenges associated with isolation and analysis, and therefore, a methodological gap exists. This article summarizes the progress in environmental NPs analysis and makes a critical assessment of whether methods from nanoparticles analysis could be adopted to bridge the methodological gap. This review discussed the sample preparation and preconcentration protocol for NPs analysis and also examines the most appropriate approaches available at the moment, ranging from physical to chemical. This study also discusses the difficulties associated with improving existing methods and developing new ones. Although microscopical techniques are one of the most often used ways for imaging and thus quantification, they have the drawback of producing partial findings as they can be easily mixed up as biomolecules. At the moment, the combination of chemical analysis (i.e., spectroscopy) and newly developed alternative methods overcomes this limitation. In general, multiple analytical methods used in combination are likely to be needed to correctly detect and fully quantify NPs in environmental samples.

The advent of the COVID-19 era has ushered in significant changes to both the environment and daily life. During the COVID-19 lockdown, a unique opportunity emerged to improve environmental quality and mitigate certain impacts on the planet. The distribution and health risks of microplastics (MPs) in the street dust of Dhaka city, Bangladesh during and after COVID-19 lockdowns were examined in this study. The study covered sites selected based on land usage, including an industrial area (IA), commercial area (CA), public facilities area (PFA), and residential area (RA). The particles in the dust samples were analyzed using a fluorescent microscope and attenuated total reflectance Fourier-transform infrared spectroscopy. The results show that the maximum number of MP particles/g of street dust sample was recorded from industrial areas (17.33 MP particles/g) and the minimum was recorded from residential areas (13.99 MP particles/g) without lockdown. The trends in the MPs were as follows: without lockdown > partial lockdown > complete lockdown. Risk analysis showed that the MPs in dust pose low non-carcinogenic risk to inhabitants of the study area and across lockdown periods. Principal component analysis showed that during the partial lockdown period, comparable sources were detected for the cellulose/low-density polyethylene (LDPE)/high-density polyethylene (HDPE), polychloroprene (PCP)/polyethylene terephthalate (PET)/polypropylene (PP)/polyacrylamide (PAA)/nylon, and polyethylene (PE)/polydimethylsiloxane (PDMS)/polyvinyl alcohol (PVA)/fiber groups of MPs, but various sources were discovered during the complete and without lockdown periods. The results further showed that all MP types would pose no non-carcinogenic or carcinogenic risks in dust from all land-use areas. However, the highest risks were obtained from inhaling dust. The study shows that human activities have a significant impact on the generation and distribution of MPs in the environment. The changes in MP type distribution during lockdown suggest that reducing human activities, such as traffic and industrial activity, can lead to a decrease in the quantity of MPs generated and released into the environment.

Airborne particulate matter (PM) pollution often occurs in the wintertime in northern China, posing a potential threat to human health. To date, there are limited studies about the metals and inorganic ions to link source apportionments and health risk assessments in the different size-segregated PM samples. In this study, our samples were collected by a high-volume air sampler from 26 December 2018 to 11 January 2019 in a high population residential area (Beijing). Water-soluble inorganic ions, metal elements in the different size-segregated PM samples were determined for health risk assessments by inhalation of PM. During the sampling period in Beijing, the average concentrations of PM_1.1 and PM_1.1–2.0 were 39.67 ± 10.66 μg m⁻³ and 32.25 ± 6.78 μg m⁻³. Distinct distribution profiles characterized the different elements. The markers of coal combustion Pb, As, and Se had >52% of their mass concentration in PM_1.1. The average mass ratios of (NO₃⁻ + NO₂⁻)/SO₄²⁻, Cl⁻/Na⁺, Cl⁻/K⁺, and Cl⁻/(NO³⁻ + NO₂⁻) were 1.68, 6.58, 6.18, and 0.57, which showed that coal combustion and vehicle emissions were the main anthropogenic sources of PM in Beijing in winter. PM_1.1 was the major contributor of Pb, Cd, and As for carcinogenic risks (CR) and hazard quotient (HQ). It was indicated that PM_1.1 is more harmful than coarse PM. The toxic elements of Cr (VI) (1.12 × 10⁻⁶), V (0.69 × 10⁻⁶), and As (0.41 × 10⁻⁶) caused higher CR for children than Ni, Cd, Co, and Pb. Meanwhile, Pb (35.30 × 10⁻⁶) and Ni (21.07 × 10⁻⁶) caused higher CR for adults than As, Cr (VI), V, Co, and Cd, especially PM_1.1. This study provides detailed composition data and the first report on human health in a high population residential area in Beijing.

The main objective of this study was to examine the chemical characteristics, possible sources, and health risks of fine particle-bound Polycyclic Aromatic Hydrocarbons (PAHs) in the Baoshan area of Shanghai. Here, ambient particles with five-size ranges were collected during the spring and late summer of 2017. The PAHs were determined by the Gas Chromatography-Mass Spectrometry (GC-MS). Our results showed that the average mass concentration of 13 species of PAHs in spring and in late summer was 4.83 (1.88~12.1) ng/m³ and 4.27 (2.09~5.75) ng/m³ in Total Suspended Particles (TSPs), respectively. The higher PAH ratios (PM_1.1/TSPs) indicated that PAHs are mainly concentrated in PM_1.1, especially in late summer. The values of BaA/(BaA+CHR) were under 0.50 and IcdP/(IcdP+BghiP) were in range from 0.20 to 0.50 for TSP and PM_1.1, suggesting that petroleum combustion and diesel emissions could be considered as key sources of PAHs, which tend to be associated with PM_1.1. Moreover, the Principal Component Analysis (PCA) in PM_1.1 identified the main PH sources, which include stationary and diesel emissions. The air mass backward trajectories and wind direction analysis showed that air masses were mainly derived from marine sources across the local industry area in late summer. Individual Carcinogenic Risk Inhalation (ILCR) was over 10⁻⁶ among the total six age groups in both of the sampling periods in TSPs, indicating the possible carcinogenic risk, especially for children and the young age group. Toxic PAHs belong to Heavy Molecular Weight (HMW) PAHs, especially Benzo[a]pyrene (BaP). Compared with PM_1.1–2.0, the Combustion-Derived PAHs group (COMPAHs) and Carcinogenic PAHs (CANPAHs) were highly concentrated in PM_1.1. Stationary sources, such as the developed steel industry, made a great contribution to the level of PAHs, especially in late summer.