We used replicated paddy microcosm systems to estimate the tropic transfer of citrate-coated silver nanoparticles (AgNP citrate), polyvinylpyrrolidone (PVP)-coated AgNP (AgNP PVP), and silver ions (AgNO₃) for 14 days under two exposure regimes (a single high-dose exposure; 60 μg L⁻¹ and a sequential low-dose exposure at 1 h, 4 days and 9 days; 20 μg L⁻¹ × 3 = 60 μg L⁻¹). Most Ag ions from AgNO₃ had dispersed in the water and precipitated partly on the sediment, whereas the two Ag NPs rapidly coagulated and precipitated on the sediment. The bioconcentration factors (BCFs) of Ag from AgNPs and AgNO₃ in Chinese muddy loaches and biofilms were higher than those of river snails in both exposure conditions. These BCFs were more prominent for 14 days exposure (7.30 for Chinese muddy loach; 4.48 for biofilm) in the low-dose group than in the single high-dose group. Their retention of AgNPs and Ag ions differed between the two exposure conditions, and uptake and elimination kinetics of Ag significantly differed between AgNP citrate and AgNP PVP in the sequential low-dose exposure. Stable isotopes analyses indicated that the trophic levels between Chinese muddy loaches and biofilms and between river snails and biofilms were 2.37 and 2.27, respectively. The biomagnification factors (BMFs) of AgNPs and AgNO₃ between Chinese muddy loaches and biofilms were significantly higher than those between river snails and biofilms under both exposure settings. The BMFs of AgNP citrate and AgNO₃ between Chinese muddy loaches and biofilms were greater than those of AgNP PVP for 14 days in the single high-dose group, whereas the BMFs of AgNP PVP were greater than those of AgNP citrate and AgNO₃ in the sequential low-dose group. These microcosm data suggest that AgNPs have the potential to impact on ecological receptors and food chains.

Exposure to PM₂.₅ is associated with an increased risk of lung diseases, and oxidative damage is the main reason for PM₂.₅-mediated lung injuries. However, little is known about the early molecular events in PM₂.₅-induced lung toxicity. In the present study, the metabolites in PM₂.₅-treated A549 cells were examined via a robust and nondestructive nuclear magnetic resonance (NMR)-based metabolic approach to clarify the molecular mechanism of PM₂.₅-induced toxicity. NMR analysis revealed that 12 metabolites were significantly altered in PM₂.₅-treated A549 cells, including up-regulation of alanine, valine, lactate, ω-6 fatty acids, and citrate and decreased levels of gamma-aminobutyric acid, acetate, leucine, isoleucine, D-glucose, lysine, and dimethylglycine. Pathway analysis demonstrated that seven metabolic pathways which included alanine, aspartate and glutamate metabolism, aminoacyl-tRNA biosynthesis, taurine and hypotaurine metabolism, arginine and proline metabolism, starch and sucrose metabolism, valine, leucine and isoleucine biosynthesis, and tricarboxylic acid cycle were mostly influenced. Our results indicate that NMR technique turns out to be a simple and reliable method for exploring the toxicity mechanism of air pollutant.

Recently, a considerable attention has been paid on the preparation of layered double hydroxide (LDH) as a green adsorbent. This research presents a study on nickel and lead removal by Ca/Fe layered double hydroxides intercalate with citrate anions (Ca-Fe/LDH-Cit) which was successfully prepared through the co-precipitation and hydrothermal method. The as-synthesized Ca-Fe/LDH-Cit was characterized by various techniques including FT-IR, XRD, TGA, FE-SEM, and TEM techniques. The maximum uptake capacities of Ca-Fe/LDH-Cit were 2.26 mg/g for Ni(II) and 61.73 mg/g for Pb(II) inferred from the Langmuir model at the contact time of 30 min and pH of 7. Based on the results, the adsorption and kinetic isotherms were in good agreement with the Langmuir model and the pseudo-second-order equation, respectively. The results suggested that the composite adsorbent has the good ability to remove the Ni²⁺ and Pb²⁺ ions from aqueous solutions. The results reveal that the composite adsorbent can be considered as a high-capacity absorbent for Ni(II) and Pb(II) removal and also as a potential candidate for practical applications.