Search

Although bats are responsible for many ecosystem services on which humans depend, they are frequently exposed to multiple anthropogenic stressors. Heavy metal (HM) exposure is an emerging threat of great significance to bats, yet the toxicity threshold for most metallic elements remains unknown. The greatest diversity of bats worldwide is in the Neotropical region, where ecotoxicological studies are scarce. Thus, this review provides a current overview of the knowledge available on HMs contamination of Neotropical bats. Analysis of the results of 17 articles published between 2000 and 2023 documented a trend of increasing interest in the topic, although it is incipient and in few countries. Of the 226 species known for the Neotropics, 95 have been investigated for metal concentrations. Seven different matrices were used to assess concentrations of heavy metals in tissues, with fur being the subject of eight studies, highlighting the search for non-invasive analysis. Twenty-one HMs were detected in bats, with mercury being the most common. The highest concentrations of this HM were detected in insectivorous/omnivorous bats, highlighting its magnification in this trophic guild compared to frugivorous bats. Copper, lead, and cadmium did not differ significantly among the other trophic guilds. This review shows that there is knowledge about concentrations of heavy metals in several Neotropical species, but knowledge about the impact of these concentrations on bat health is limited, which highlights the need for research to determine critical concentrations that cause damage to bat health, and that guide conservation actions for their populations, as well as environmental monitoring actions for these pollutants., (© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)

Background: Statins present a plethora of pleiotropic effects including anti-inflammatory and antimicrobial responses. A,α-difluorophenylacetamides, analogs of diclofenac, are potent pre-clinical anti-inflammatory non-steroidal drugs. Molecular hybridization based on the combination of pharmacophoric moieties has emerged as a strategy for the development of new candidates aiming to obtain multitarget ligands., Methods: Considering the anti-inflammatory activity of phenylacetamides and the potential microbicidal action of statins against obligate intracellular parasites, the objective of this work was to synthesize eight new hybrid compounds of α,α-difluorophenylacetamides with the moiety of statins and assess their phenotypic activity against in vitro models of Plasmodium falciparum and Trypanosoma cruzi infection besides exploring their genotoxicity safety profile., Results: None of the sodium salt compounds presented antiparasitic activity and two acetated compounds displayed mild anti- P. falciparum effect. Against T. cruzi , the acetate halogenated hybrids showed moderate effect against both parasite forms relevant for human infection. Despite the considerable trypanosomicidal activity, the brominated compound revealed a genotoxic profile impairing future in vivo testing., Conclusions: However, the chlorinated derivative was the most promising compound with chemical and biological profitable characteristics, without presenting genotoxicity in vitro , being eligible for further in vivo experiments.

The current work assessed the degradation degree and the degradation products derived from norfloxacin (NOR) and gentamicin (GEN) using iodosylbenzene and iodobenzene diacetate, in the presence of manganese porphyrin as catalysts. Better results for NOR degradation (> 80%) were obtained when more hydrophobic porphyrins were employed. β-brominated manganese porphyrins showed a lower GEN degradation (~ 25%) than the non-brominated ones (~ 35%), probably due to their steric hindrance. In any case, complete mineralization was achieved neither for NOR nor for GEN, and the assignment of the generated products, complemented by the study of their toxicity, was an important step performed. From the obtained results, no correlation was found between the number of identified products and the reported toxicity value (r Spearman,NOR  = 0.006; p value = 0.986 and r Spearman,GEN  =  - 0,198; p value = 0.583), which reinforces the idea of synergism and antagonistic phenomena. The higher degradation degree could have led to products of lower steric hindrance and easier penetration into the A. fischeri cells, which subsequently led to an increase in toxicity for these experiments. In most cases, the products presented higher toxicity than the original compound, which raises a concern about their occurrence in environmental matrices., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Pharmaceutically active compounds are increasingly detected in raw and treated wastewater, surface water, and drinking water worldwide. These compounds can cause adverse effects to the ecosystem even at low concentrations and, to assess these impacts, toxicity tests are essential. However, the toxicity data are scarce for many PhACs, and when available, they are dispersed in the literature. The values of pharmaceuticals concentration in the environment and toxicity data are essential for measuring their environmental and human health risks. Thus this review verified the concentrations of pharmaceuticals in the aquatic environment and the toxicity related to them. The risk assessment was also carried out. Diclofenac, naproxen, erythromycin, roxithromycin, and 17β-estradiol presented a high environment risk and 17α-ethinylestradiol presented a high human health risk. This shows the potential of these pharmaceuticals to cause adverse effects to the ecosystem and humans and establishes the necessity of their removal through advanced technologies., (Copyright © 2021. Published by Elsevier Ltd.)

Phenolic compounds are widely spread in surface water, mainly in developing countries, where sewage and wastewater treatment are still reduced. Thus, this work quantified these pollutants in the Doce River analyzing the associated risk for the environment and human health. This river is in the state of Minas Gerais in Brazil and was recently impacted by the collapse of a mining dam that compromised the resilience of the entire watershed. For that purpose, a methodology for simultaneous identification and quantification of 17 different phenols was developed. It was possible to verify phenolic compounds' occurrence with concentration ranging from 0.13 to 24.16 µg·L -1 . 2-Nitrophenol and bisphenol A appeared in all samples analyzed. The analytical method was processed using solid-phase extraction (SPE) (C 18 cartridge), gas chromatography with FID, and mass spectrometry to define the analytes' retention time. For case validation, the selectivity, linearity, detection and quantification limits, sensitivity, precision, accuracy, resolution, matrix effect, and peak quality were assessed. Four different solvents were tested in the recovery-grade trials, which were dichloromethane, methanol, acetonitrile, and ethyl acetate. Among them, methanol had a better performance and was used throughout all analyses. The phenolic compounds had a recovery degree higher than 50% after SPE, regardless of the matrices., (© 2021. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)

The present study had the objective to investigate the equilibrium, kinetics, thermodynamic viability and system optimization of methylene blue (MB) and eriochrome black T (ET) biosorption onto Fucus vesiculosus ( F. vesiculosus ). A comprehensive bioadsorbent characterization was carried out. The infrared spectra suggested a physical biosorption mechanism that was later proven by the enthalpy change and the isotherms models. Furthermore, the process was best described by Langmuir and Temkin isotherm models, indicating the monolayer formation and the linear reduction of the heat of biosorption with the coverage degree. F. vesiculosus presented a maximum biosorption capacity of 698.477 mg·g -1 for MB, and 24.306 mg·g -1 for ET. Regarding kinetics, the pseudo-second-order kinetic model was the best fitted model. In addition, the film diffusion was confirmed as the process limiting step. The model's optimization was achieved in order to maximize the removal efficiency, corresponding to 99.28% for MB and 99.44% for ET.

High consumption of drugs, combined with their presence in the environment, raises concerns about its consequences. Even though researches are often engaged in analyzing substances separately, that is not the environmental reality. Therefore, the aim of this study was to investigate the acute toxicity of the pharmaceuticals simvastatin, metformin, omeprazole and diazepam, and all possible mixtures between them, to the organism Aliivibrio fischeri, verifying possible synergistic or antagonistic effects and assessing byproducts formation. In terms of individual toxicity, omeprazole is the most toxic of the active ingredients, followed by simvastatin, diazepam and, finally, metformin. When the toxicity of mixtures was tested, synergism, antagonism and hormesis were perceived, most probably generated due to byproducts formation. Moreover, it was observed that even when compounds are at concentrations below the non-observed effect concentration (NOEC), there may be toxicity to the mixture. Hence, this work points to the urgent need for more studies involving mixtures, since chemicals are subject to interactions and modifications, can mix, and potentiate or nullify the toxic effect of each other.

In the present study, the simultaneous adsorption degradation of norfloxacin (NOR) by graphene oxide from aqueous matrix was verified. Graphene oxide (GO, ~ 8 layers) was prepared using modified Hummers method through the oxidation/exfoliation of expanded graphite. Spectroscopic techniques confirmed the NOR adsorption onto GO surface and the partial antibiotic degradation promoted by hydroxyl radicals derived from GO. Furthermore, the mass spectra after the adsorption-degradation processes showed NOR degradation intermediates that was compared and confirmed by other studies. The nanomaterial showed a removal capacity of 374.9 ± 29.8 mg g -1 , observing greater contribution from the NOR in the zwitterionic form and removals up to 94.8%. The intraparticle diffusion process, assessed by Boyd's model and Fick's law, presented a greater contribution in the removal process, reaching the equilibrium 30 min after the beginning. In addition, the temperature increase would disadvantage the process, which was considered thermodynamically viable throughout the evaluated temperature range. Finally, the process was scaled-up in a single stage batch adsorber considering a NOR removal efficiency of 95%. This resulted in mass requirement of 63.6 g of GO in order to treat 0.5 m 3 of contaminated water. In general, the simultaneous adsorption-degradation process was considered innovative and promising in pharmaceutical compounds remediation.

The purpose of studying the biodegradability of pharmaceutical compounds is to evaluate their behaviors in relation to the treatment processes generally used in domestic and industrial wastewater treatment plants. The antibiotic norfloxacin was found to be a recalcitrant compound. The studies conducted showed norfloxacin removal rates of 12% and 18% when biomasses from treatments with activated sludge and anaerobic biodigesters, respectively, were used without acclimatization. This suggests that anaerobic digestion shows better performance for norfloxacin removal. Ecotoxicological tests, using the luminescent marine bacteria Aliivibrio fischeri as the test organism, show that anaerobic digestion could eliminate the toxicity of the antibiotic norfloxacin, even though total degradation of the drug was not observed. The release of norfloxacin during cell lysis suggests the importance of controlling this phenomenon in biological treatment systems that handle wastewater contaminated with norfloxacin, thus preventing the return of this drug to the environment.