RESUMEN

Dietary antioxidants, including 2,6-di-tert-butyl-hydroxytoluene (BHT), α-tocopherol (αT) and tea polyphenol (TP), have been widely used in food. However, no data about the effect of food antioxidants on PFOA excretion were available. In this study, excretion of PFOA toward mice (four mice in each group) under the influence of co-ingested food antioxidants (i.e., BHT, αT, and TP) were investigated, and mechanism involved in excretion of PFOA, including RNA expression of uptake and efflux transporters in kidneys and liver involved in PFOA transport and intestinal permeability were also investigated. Chronic exposure to BHT (1.56 mg/kg) increased urinary PFOA excretion from 1795 ± 340 ng/mL (control) to 3340 ± 29.9 ng/mL (BHT treatment). TP treatment (12.5 mg/kg) decreased urinary excretion of PFOA, i.e., with a decrease percentage of 70% compared to the control. Organic anion transporting polypeptides (Oatps) act as uptake transporter mediate renal elimination or reabsorption of PFOA in the kidney. The decrease in urinary excretion of PFOA under TP treatment was associated with significantly (p < 0.05) enhanced expression of Oatp1a1 in the kidney (1.78 ± 0.58 vs 1.00 ± 0.18 in control), which facilitated renal reabsorption of PFOA and in turn decreased urinary excretion of PFOA. αT treatment (12.5 mg/kg) increased fecal PFOA excretion with a value of 228 ± 95.8 ng/g vs control (96.8 ± 22.7 ng/g). Mechanistic investigation revealed that αT treatment reduced intestinal permeability, resulting in increased fecal PFOA excretion.

RESUMEN

Understanding the sources of antibiotics is important for managing antibiotic contamination and preventing environmental risks in the aquatic environment. In this study, the distribution of dissolved organic matter (DOM) and 24 antibiotics from four typical classes (quinolones, macrolides, sulfonamides and tetracyclines) in the Yellow River basin containing distinct sources of pollution was investigated. In particular, relationships between the antibiotic concentrations and fluorescent properties of DOM were to be established to identify antibiotic sources. A total of 22 antibiotics were detected, with maximum concentrations ranging from 0.27 to 30.14 ng/L in the mainstream of the Yellow River. Of these antibiotics, only erythromycin (ERY) and sulfamethoxazole (SMX) posed potential risks to aquatic organisms. Spatially, tetracyclines were mainly distributed in the upstream reaches of the river, and quinolones were largely distributed in the midstream. High levels of sulfonamides were present downstream of the investigated river. Only EYR belonging to the macrolide group was detected and had a high downstream concentration. EEM-PARAFAC analysis showed that DOM was composed of visible fulvic acid-like fluorescence fraction (C1), ultraviolet fulvic acid-like fluorescence fraction (C2) and protein-like fraction (C3). Using Pearson correlation analysis, this study demonstrated a close relationship between DOM spectral parameters and antibiotic concentrations in the Yellow River basin. Specifically, r (C3, C2) was significantly and positively correlated with the concentrations of SMX, sulfadoxine (SDX), and ERY, while humification index (HIX) had an opposite relationship with these antibiotics. These results suggested that SMX, SDX and ERY were mainly discharged from wastewater treatment plants into the mainstream of the Yellow River. This work provides a powerful demonstration that DOM plays an important role in indicating the occurrence and sources of antibiotics in the aquatic environment.

Asunto(s)

Antibacterianos , Materia Orgánica Disuelta , Antibacterianos/análisis , Sulfanilamida , Eritromicina , China , Sulfametoxazol , Sulfadoxina , Sulfonamidas , Espectrometría de Fluorescencia

RESUMEN

Understanding the occurrence and fate of antibiotics from different categories is vital to predict their environmental exposure and risks. This study presents the spatiotemporal occurrence of 45 multi-class antibiotics and their associations with suspended particulate matter (SPM) in Xiaoqing River (XRB) and Yellow River (YRB) via 10-month monitoring in East China. Thirty-five and 31 antibiotics were detected in XRB and YRB, respectively. Among them, fluoroquinolones (FQs) had the highest total mean concentration (up to 24.8 µg/L in XRB and 15.4 µg/L in YRB), followed by sulfonamides (SAs) (14.0 µg/L and 15.4 µg/L) and macrolides (MLs) (1.1 µg/L and 1.6 µg/L). Significant spatial-temporal variations were found in both rivers where higher concentrations of antibiotics were observed in urban and densely populated areas during winter and spring. Hydrological factors such as river flow and water volume, instream attenuation and antibiotic usage may cause the observed variabilities in the seasonal patterns of antibiotic pollution. Using linear regression analysis, for the first time, this study confirmed that the total concentrations of MLs (p < 0.05), FQs (p < 0.001) and SAs (p < 0.001) were strongly correlated with the turbidity/total suspended solids in the studied rivers (except MLs in YRB). It is thus suggested that partitioning processes onto SPM might affect the distribution of detected antibiotics in rivers, which are largely dependent on SPM composition and characteristics. The risk quotient (RQ) determined for up to 87 % of individual compound was below 0.1 in both rivers; however, the high joint toxicity reflected by the mixed RQs of detected antibiotics may rise risk alarm for aquatic species. Further aspects regarding active mechanisms of SPM-antibiotic interactions and ecological risks of coexistence of multiple antibiotics need to be investigated.

Asunto(s)

Ríos , Contaminantes Químicos del Agua , Antibacterianos/análisis , Material Particulado/análisis , Sedimentos Geológicos , Monitoreo del Ambiente , Estaciones del Año , Contaminantes Químicos del Agua/análisis , Fluoroquinolonas/análisis , Macrólidos/análisis , Sulfonamidas/análisis , Agua/análisis , China

RESUMEN

Sewage treatment plants (STPs) and pharmaceutical manufactories (PMFs) are recognized as important reservoirs for aquatic pollution with antibiotics. Although the occurrence of multiple classes of antibiotics has been mostly reported for STPs and PMFs, knowledge on the effects of wastewater treatment processes on the removal of antibiotics is not well documented. In this study, wastewaters were collected from different treatment points of two STPs and two PMFs in eastern China. Thirty-seven antibiotics within the four classes of fluoroquinolones (FQs), macrolides (MACs), sulfonamides (SAs) and tetracyclines (TCs) were analyzed. Among the investigated antibiotics, 19-33 out of 37 target compounds were detected at least once in the STPs wastewaters ranging from low ng/L to approximately 12.7 µ/L. In the wastewater samples collected from PMFs, up to 34 antibiotics were present with detection frequencies up to 100%, showing generally higher concentrations (up to 19.0 µ/L) than those at the STPs. FQs and SAs were the dominant antibiotic families, which accounted for more than 90% of the total antibiotic concentration in the wastewaters. Moreover, the removal of antibiotics by anaerobic-anoxic-oxic (A2O), membrane bioreactor (MBR) and conventional activated sludge (CAS) systems was evaluated. The MBR system exhibited the best performance, mainly due to the processes of biodegradation and sorption during biological treatments. Notably, several SAs (SMP, SMZ) and FQs (CIN, ENO) antibiotics were consistently detected at concentration levels of µ/L in the effluent samples. The culturable antibiotic-resistance tests and risk assessment indicated that the antibiotic-contaminated effluents would facilitate the development of resistant bacteria and pose high toxicity to non-target organisms in the aquatic environment. Overall, the findings suggested an urgent need for improving the wastewater treatment technologies for simultaneous removal of different classes of antibiotics.

Asunto(s)

Aguas Residuales , Contaminantes Químicos del Agua , Antibacterianos , Biodegradación Ambiental , China , Industria Farmacéutica , Humanos , Aguas del Alcantarillado/análisis , Eliminación de Residuos Líquidos , Contaminantes Químicos del Agua/análisis

RESUMEN

Leaching dynamics of dissolved organic matter (DOM) from agricultural soil are influenced by the chemistry of irrigation water. This study used multiple spectroscopy methods to investigate the dynamics of DOM in column leaching process by utilizing selected solutions. DOC was leached out by Na solutions more effectively than by Ca, despite the additional contributions of the ligand exchange of SO42- and the hydrolysis of HCO3-. The concentration ranking corresponding to solutions is Na2SO4 > NaHCO3 > NaCl > CaCl2. Furthermore, the aromaticity and molecular weights of DOM leached by Na solutions increased with the leaching, whereas contrary trends were reared by Ca. Thus, specific cation substantially affects DOM concentration and composition. Parallel factor analysis of the three-dimensional fluorescence spectra (EEM-PARAFAC) determined the characteristics of DOM components. (1) The long-wavelength, humic-like components (HLC, i.e., C1, C3, and C5) were largely accumulated at the early water saturating stage but attenuated toward dynamic stability in the salt-solution leaching (SSL) stage. (2) Reactive functional group-related HLC (i.e., C2, and C4) remarkably increased in response to the solutions chemistry. (3) The protein-like component (PLC, i.e., C6) was released with insignificant dynamic differences between the solutions. Despite approximately stable DOC concentration at the late stage of each SSL, HLC exhibited accelerating release in sodium salts but declining trend in calcium salt whereas PLC showed a roughly constant dynamic in the both. Ca-bridging reactions with the detachment of OM-Ca-clay complex prompting HLC release and its formation to stabilize the HLC well explain the contrast dynamics of HLC with Na or Ca leaching. The diffusion process that was defined for the slow, lasting and small concentration of leaching of inactive components could contribute to the steady dynamic of PLC, given its insensitivity to either the salt cation. This study identified distinct release kinetics of DOM compositions from those of DOC by EEM-PARAFAC and correspondingly the potential mechanisms, which offers promising advantages in monitoring DOM transport and fractionation in dynamic leaching process.