Antibiotics have a wide application range in human and veterinary medicines. Being designed for pharmacological stability, most antibiotics are recalcitrant to biodegradation after ingestion and can be persistent in the environment. Antibiotic residues have been detected as contaminants in various environmental compartments where they cause human and environmental threats, notably with respect to the potential emergence and proliferation of antibiotic-resistant bacteria. An important component of managing environmental risk caused by antibiotics is to understand exposure of soil and water resources to their residues. One challenge is to gain knowledge on the fate of antibiotics in the ecosystem along the soil-water continuum, and on the collateral impact of antibiotics on environmental microorganisms responsible for crucially important ecosystem functions. In this context, the ANTIBIOTOX project aims at studying the environmental fate and impact of two antibiotics of the sulfonamide class of antibiotics, sulfamethazine (SMZ), and sulfamethoxazole (SMX).

Streptomycin used in human and veterinary medicine is released into the environment mainly through excretions. As such, its elimination in water should be investigated to control pollution. In this study, the degradation of streptomycin in water was studied, and the influence of variables, including light exposure, solution pH, temperature, ionic strength, dissolved organic matter (DOM), and coexisting surfactants, on degradation was investigated. Streptomycin degradation was consistent with the first-order model in aquatic environments. Its degradation rate under light exposure was 2.6-fold faster than that in the dark. Streptomycin was stable under neutral conditions, but it was easily decomposed in acidic and basic environments. Streptomycin degradation was enhanced by high temperature, and its half-life decreased from 103.4 days at 15 °C to 30.9 days at 40 °C. This process was also accelerated by the presence of Ca²⁺ and slightly improved by the addition of HA. Streptomycin degradation was suppressed by high levels of the cationic surfactant cetyltri- methylammonium bromide (CTAB), but was promoted by the anionic surfactant sodium dodecyl benzene sulfonate (SDBS). The main degradation intermediates/products were identified through liquid chromatography–mass spectrometry, and the possible degradation pathway was proposed. The antibacterial activity of streptomycin solution was also determined during degradation. Results showed that STR degradation generated intermediates/products with weaker antibacterial activity than the parent compound.

The objective of this work was to evaluate the efficiency of a solar TiO₂-assisted photocatalytic process on amoxicillin (AMX) degradation, an antibiotic widely used in human and veterinary medicine. Firstly, solar photolysis of AMX was compared with solar photocatalysis in a compound parabolic collectors pilot scale photoreactor to assess the amount of accumulated UV energy in the system (QUV) necessary to remove 20 mg L⁻¹AMX from aqueous solution and mineralize the intermediary by-products. Another experiment was also carried out to accurately follow the antibacterial activity against Escherichia coli DSM 1103 and Staphylococcus aureus DSM 1104 and mineralization of AMX by tracing the contents of dissolved organic carbon (DOC), low molecular weight carboxylate anions, and inorganic anions. Finally, the influence of individual inorganic ions on AMX photocatalytic degradation efficiency and the involvement of some reactive oxygen species were also assessed. Photolysis was shown to be completely ineffective, while only 3.1 kJUV L⁻¹was sufficient to fully degrade 20 mg L⁻¹AMX and remove 61 % of initial DOC content in the presence of the photocatalyst and sunlight. In the experiment with an initial AMX concentration of 40 mg L⁻¹, antibacterial activity of the solution was considerably reduced after elimination of AMX to levels below the respective detection limit. After 11.7 kJUV L⁻¹, DOC decreased by 71 %; 30 % of the AMX nitrogen was converted into ammonium and all sulfur compounds were converted into sulfate. A large percentage of the remaining DOC was in the form of low molecular weight carboxylic acids. Presence of phosphate ions promoted the removal of AMX from solution, while no sizeable effects on the kinetics were found for other inorganic ions. Although the AMX degradation was mainly attributed to hydroxyl radicals, singlet oxygen also plays an important role in AMX self-photosensitization under UV/visible solar light.

Emamectin benzoate (EMB), which is used as a pesticide in agriculture, household, and veterinary medicine, can cause tissue damage with oxidative toxicity and can be considered as inducing apoptosis. In the present study, male mice were conducted by oral administration in EMB doses 25, 50, and 100 (mg/kg/day) for 14 days. Glutathione (GSH) and thiobarbituric acid reactive substance (TBARS) levels using spectrophotometric methods were measured. 8-hydroxy-2′-deoxyguanosine (8-OHdG) which is DNA oxidation biomarker and, stress protein (HSP70) levels, caspase 3 enzyme activities were measured by ELISA techniques. This study shows that in vivo administration of EMB caused a marked induction of oxidative damage in liver tissue as demonstrated by an increased level of TBARS and reduced GSH level. The increase in HSP70 level did not prevent the apoptosis caused by the increase of caspase 3 enzyme activity. Toxicity caused by EMB also showed the formation of genotoxicity with an increase in DNA oxidation biomarker 8-OHdG levels. As a result of the study, the effects of toxicity caused by EMB on lipid; protein; and DNA, structural macromolecules in cells, and the importance of enzymatic and non-enzymatic bonds of the cell’s protective systems were determined. Consequently, under experimental conditions, EMB exposure caused toxicity in the liver of male mice, and significant adverse effects were determined with biomarkers.

The extensive use of insecticides has hazardous effects since they can damage human health as well as the environment. Abamectin has been widely used in veterinary medicine and as a pesticide in agriculture. It is considered as one of the most commonly used insecticides in Egypt. The focus of the present study is to examine the toxic effects of sublethal dose (1 mg/kg b.wt.) of abamectin (Crater 3.37% EC) in male albino rats and to evaluate the efficiency of Eruca sativa suspension to ameliorate the abamectin toxicity. The present study was achieved using 18 male albino rats. Rats were divided into three groups: normal control group, abamectin-treated group, and abamectin + E. sativa-treated group. Rats of the third group were orally administrated a mixture of sublethal dose of abamectin (1 mg/kg b.wt.) and E. sativa suspension (5 g/kg b.wt.) three times a week for 28 days. At the end of the study period, blood samples were collected from all groups to measure the various hematological and biochemical parameters. The results revealed that rats, after abamectin exposure, exhibited general signs of toxicity and disturbance in the hematological and biochemical parameters. In addition, administration of E. sativa suspension ameliorated the hematological and biochemical parameters. These findings suggested that the exposure to abamectin might be responsible for hypertension, liver and kidney dysfunction, lipid profile disturbance, and oxidative stress, reflected in hematological and biochemical parameters. It was also found that the administration of E. sativa suspension reduced the detrimental impact of abamectin on some hematological and biochemical parameters.