The potential persistence and migration of 14 antibiotics comprising sulfonamides, fluoroquinolones, macrolides and tetracyclines were conducted using a 50-d recirculating flume study supported by batch attenuation experiments with spiked concentrations. The study demonstrated that photodegradation was the dominant attenuation process for these antibiotics in the water environment. The half-lives of 2–26 d were in order of sulfadiazine > sulfadimethoxine > sulfamerazine > sulfamethoxazole > sulfamethazine > sulfathiazole > ofloxacin > enrofloxacin > norfloxacin > ciprofloxacin > erythromycin > tetracycline > roxithromycin > oxytetracycline. These modest half-lives meant that the antibiotics were predicted to travel 30–400 km down a typical river before half the concentration would be lost. All antibiotics were detected on the surface sediment in the flume study. Under hyporheic exchange, some of them continually migrated into the deeper sediment and also the sediment pore water. All fluoroquinolones were detected in the sediments. The sulfonamides were detected in the pore water with relatively high concentrations and frequencies. Sulfadiazine, sulfamethazine and sulfathiazole in the upper layer pore water were found to be approaching equilibrium with the surface water. The high presence of sulfonamides in the pore water indicated that their high mobility and persistence potentially pose a risk to hyporheic zone.

We investigated the effect of solution pH and soil structure on transport of sulfonamide antibiotics (sulfamethoxazole, sulfadimethoxine and sulfamethazine) in combination with batch sorption tests and column experiments. Sorption isotherms properly conformed to Freundlich model, and sorption potential of the antibiotics is as follows; sulfadimethoxine > sulfamethoxazole > sulfamethazine. Decreasing pH values led to increased sorption potential of the antibiotics on soil material in pH range of 4.0–8.0. This likely resulted from abundance of neutral and positive-charged sulfonamides species at low pH, which electrostatically bind to sorption sites on soil surface. Due to destruction of macropore channels, lower hydraulic conductivities of mobile zone were estimated in the disturbed soil columns than in the undisturbed soil columns, and eventually led to lower mobility of the antibiotics in disturbed column. The results suggest that knowledge of soil structure and solution condition is required to predict fate and distribution of sulfonamide antibiotics in environmental matrix.

This study evaluated the occurrence of 36 PPCPs in urban river water samples collected from Beijing, Changzhou and Shenzhen. Twenty-eight compounds were detected. Compounds found with highest median concentrations included: sulfadimethoxine (164 ng/L), sulpiride (77.3 ng/L), atenolol (52.9 ng/L), and indomethacin (50.9 ng/L). Antibiotic was the predominant class detected and contributed about half of the overall PPCPs contamination level. Effluents from wastewater treatment plants (WWTPs) were demonstrated to be the predominant pathways through which PPCPs entering into aquatic environment in all investigated areas. The ratio of persistent PPCPs like sulpiride and carbamazepine was identified to be feasible in tracing their contamination sources in rivers. Concentrations of most detected PPCPs showed significant positive correlations with total nitrogen and total phosphorus. Two groups of representative PPCPs were selected as the chemical indicators for predicting the overall PPCPs contamination, based on the significant correlations between PPCPs.

Residual antibiotics in land-applied manure and biosolids present a potential threat to public and ecological health. It remains important to determine antibiotic degradation efficiencies for manure and biosolids waste management practices and to identify conditions that enhance antibiotic degradation. The fates of the antibiotics florfenicol, sulfadimethoxine, sulfamethazine, and tylosin were studied during pilot-scale static pile thermophilic composting, and the effects of temperature and feedstock particles on antibiotic degradation rates were tested. The antibiotics were spiked into dairy manure solids and wastewater biosolids, and treatments included aerated and non-aerated manure and biosolids/wood-product (1:3 v/v) composting. Results showed no significant differences between aerated and non-aerated treatments; on average, ≥85, ≥93, and ≥95 % antibiotic degradation was observed after 7, 14, and 21 days of composting. Greater antibiotic degradation was observed in manure compost compared to biosolids compost for florfenicol (7, 14, 21, 28 days) and tylosin (14, 28 days); however, there was no significant difference for sulfadimethoxine and sulfamethazine. Peak temperatures were 66–73, and ≥55 °C was maintained for 6–7 days in the biosolids compost and 17–20 days in the manure compost. Bench-scale experiments conducted at 25, 55, and 60 °C showed that lower temperature decreased degradation of the sulfonamides and tylosin in both feedstocks and florfenicol in the biosolids. The presence of compost particles increased antibiotic degradation, with time to 50 % degradation ≤2 days in the presence of solids (60 °C) compared to no degradation in their absence. These results indicate that thermophilic composting effectively degrades parent antibiotic compounds in manure and biosolids.

Extraction and analysis methods have been developed for the detection of the following four antibacterial agents and two natural estrogens in treated municipal wastewater sludge and commercial compost: sulfamethoxazole (SMX), sulfadimethoxine (SDM), tetracycline (TET), oxytetracycline (OXY), estrone (E1), and 17β-estradiol (E2). The antibiotics and estrogens were extracted from secondary sludge and mixed compost using ultrasonic solvent extraction. Citric acid (pH 4.7) and methanol were used as extraction buffer, followed by tandem-solid-phase extraction cleanup, strong anion exchange + hydrophilic–lipophilic balance for antibiotics and CarboPrep/NAX for estrogens. For quantification, two different methods were employed, using HPLC–MS/MS, with an electrospray ionization source for antibiotics and an atmospheric-pressure chemical ionization source for estrogens. Recoveries were 11–31% for the sulfonamides (SMX and SDM) and tetracyclines (TET and OXY) and 30–59% for the estrogens (E1 and E2) over the entire method. Limits of detection for the extraction method were in the nanogram per gram range for dry weight sludge and compost samples. Neither of the two sulfonamide antibiotics was detected in secondary sludge or mixed compost samples. Estrogens were found in compost in amounts of 160 ± 65 ng/g (E1) and 21 ± 3 ng/g (E2), but not in sludge. The tetracyclines, as well as what is believed to be the 4-epimer of OXY, were found in both sludge and compost in amounts of 1.57 ± 0.67 and 2.95 ± 0.42 μg/g (TET), 0.56 ± 0.12 and 6.51 ± 0.52 μg/g (OXY), and 7.60 ± 1.68 and 1.35 ± 0.24 μg/g (4-epi-OXY), respectively. These results indicate that sorption-prone compounds are not removed during the wastewater treatment process and can persist through sludge digestion and that the composting process does not sufficiently eliminate these particular contaminants. Thus, biosolids (even composted) are an additional source of drug residues leaching into the environment, and it must be considered while using biosolids as fertilizer.

Sulfadimethoxine (SDM) is an antibiotic commonly used in concentrated animal feeding operations and released into the environment via manure application on agricultural lands. Transformation of antibiotics in soil impacts the likelihood of their entry to water bodies, uptake by plants, and thus their effect on terrestrial and aquatic organisms. We conducted experiments to incubate SDM in a sandy loam soil in the presence of humification enzymes commonly found in natural soil, laccase, horseradish peroxidase, and lignin peroxidase. Incubation with the enzymes led to significant reduction in the fraction of SDM extractable from soil, indicating the formation of bound residues. Such transformation was enhanced when the organic matter content in soil is increased or when certain chemical mediators were used along with laccase. The study provided a basis for understanding the environmental fate of sulfonamides and help with the development of remediation methods to mitigate the release of sulfonamides from soil to water.

Degradation of three sulfonamides (SAs), namely sulfamethoxazole (SMX), sulfamethazine (SMZ), and sulfadimethoxine (SDM) in surface water and sediments collected from Taihu Lake and Dianchi Lake, China was investigated in this study. The surface water (5–10 cm) was collected from the east region of Taihu Lake, China. Two sets of degradation experiments were conducted in 3-L glass bottles containing 2 L of fresh lake water and 100 μg/L of individual SAs aerated by bubbling air at a rate of approximately 1.2 L/min, one of which was sterilized by the addition of NaN₃ (0.1 %). Sediment samples were taken from Taihu Lake and Dianchi Lake, China. For the sediment experiment, 5 g of sediment were weighed into a 50-mL glass tube, with 10 mg/kg of individual SAs. Different experimental conditions including the sediment types, sterilization, light exposure, and redox condition were also considered in the experiments. The three SAs degraded in lake water with half-lives (t ₁/₂) of 10.5–12.9 days, and the half-lives increased significantly to 31.9–49.8 days in the sterilized water. SMZ and SDM were degraded by abiotic processes in Taihu and Dianchi sediments, and the different experimental conditions and sediments characteristics had no significant effect on their declines. SMX, however, was mainly transformed by facultative anaerobes in Taihu and Dianchi sediments under anaerobic conditions, and the degradation rate of SMX in non-sterile sediment (t ₁/₂ of 9.6–16.7 days) were higher than in sterilized sediment (t ₁/₂ of 18.7–135.9 days). Under abiotic conditions, degradation of SMX in Dianchi sediment was faster than in Taihu sediment, probably due to the higher organic matter content and inorganic photosensitizers concentrations in Dianchi sediment. High initial SAs concentration inhibited the SAs degradation, which was likely related to the inhibition of microorganism activities by high SAs levels in sediments. Results from this study could provide information on the persistence of commonly used sulfanomides antibiotics in lake environment.

Retention and transport of sulfonamides (SAs) in subsurface can strongly affect groundwater quality. In this work, a range of laboratory batch sorption and column transport experiments were conducted to determine the effect of cation type in mixed Ca-Na systems on the retention and transport of two typical SAs, sulfadimethoxine (SDM) and sulfacetamide (SCA), in saturated limestone porous media. Column experimental data showed divalent cation Ca²⁺ played a more important role than monovalent cation Na⁺ in decreasing the transport of only SDM in co-cation systems in the saturated limestone media. Further, in the single-cation (i.e., including either Ca²⁺ or Na⁺) system, increasing ionic strength (IS) of either NaCl or CaCl₂ had little effect on SCA transport; however, increasing of IS of CaCl₂ promoted the retention of SDM in the saturated limestone porous media. This is mainly due to the cation bridging effect of Ca²⁺ on SDM and limestone. Overall, SDM showed much higher retention in the limestone columns than SCA, which can be attributed to the two SAs’ different physicochemical properties. Moreover, limestone showed stronger ability to retain the two SAs than quartz sand. Findings in this study suggest that cation type and the concentration of certain electrolyte (e.g., CaCl₂) as well as medium type play an important role in controlling the environmental fate and transport of antibiotics.

Mangroves represent a special coastal vegetation along the coastlines of tropical and subtropical regions. Sulfonamide antibiotics (SAs) are the most commonly used antibiotics. The application of white-rot fungi extracellular enzyme-containing microcapsules (MC) for aerobic degradation of SAs in mangrove sediments was investigated in this study. Degradation of three SAs, sulfamethoxazole (SMX), sulfadimethoxine (SDM), and sulfamethazine (SMZ), was enhanced by adding MC to the sediments. The order of SA degradation in batch experiments was SMX > SDM > SMZ. Bioreactor experiments revealed that SA removal rates were higher with than without MC. The enhanced SA removal rates with MC persisted with three re-additions of SAs. Thirteen bacteria genera (Achromobacter, Acinetobacter, Alcaligenes, Aquamicrobium, Arthrobacter, Brevundimonas, Flavobacterium, Methylobacterium, Microbacterium, Oligotropha, Paracoccus, Pseudomonas, and Rhodococcus) were identified to be associated with SA degradation in mangrove sediments by combination of next-generation sequencing, bacterial strain isolation, and literature search results. Results of this study suggest that MC could be used for SA removal in mangrove sediments.

Sulfonamides are the second most widely used group of veterinary antibiotics which are often detected in the environment. They are eliminated from freshwaters mainly through photochemical degradation. The toxicity of sulfadimethoxine (SDM) was evaluated with the use of Lemna minor before and after 1- and 4-h irradiation in a SunTest CPS+ solar simulator. Eight endpoints consisting of: number and total area of fronds, fresh weight, chlorophylls a and b, carotenoids, activity of catalase and guaiacol peroxidase, and protein content were determined. The total frond area and chlorophyll b content were the most sensitive endpoints with EC50 of 478 and 554 μg L⁻¹, respectively. The activity of guaiacol peroxidase and catalase increased at SDM concentrations higher than 125 and 500 μg L⁻¹, respectively. The SDM photodegradation rate for first order kinetics and the half-life were 0.259 h⁻¹ and 2.67 h, respectively. The results show that the toxicity of irradiated solutions was caused by SDM only, and the photoproducts appeared to be either non-toxic or much less toxic to L. minor than the parent compound. To study the recovery potential of L. minor, after 7 days exposure in SDM solutions, the plants were transferred to fresh medium and incubated for the next 7 days. L. minor has the ability to regenerate, but a 7-day recovery phase is not sufficient for it to return to an optimal physiological state.