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Toxoplasmosis, a disease caused by the apicomplexan parasite Toxoplasma gondii, affects up to one third of the global population. Although immunocompetent individuals rarely experience severe symptoms, those with immunodeficiencies may potentially face fatal disease. The frontline treatments are currently sulphadiazine and pyrimethamine, which suffer from adverse side effects, and lack efficiency in clearing parasite cysts from the muscles and brain of patients. To address the need for novel, more effective, and less toxic treatments, four new ferrocenyl benzimidazole complexes 15–18 were synthesised and evaluated against the ΔKu80:mNeonGreen strain of T. gondii. Complexes 15 and 17 were found to be active with EC50 values of 17.9 and 17.5 μM respectively, with comparable activity to pyrimethamine, which had an EC50 value of 13.8 μM, and less effective than sulphadiazine, which had an EC50 value of 2.56 μM. Additionally, the compounds were found to be relatively non-toxic against HEK 293T and PNT1A human cell lines. Further investigations found that the complexes act by generating reactive oxygen species (ROS) through the ferrocenyl moiety. These complexes show potential for the development of new treatments against Toxoplasmosis. [ABSTRACT FROM AUTHOR]

A novel SrWO4-poly(3,4-ethylene dioxythiophene) (PEDOT)-polypyrrole (PPy) nanocomposite was synthesized via chemically oxidative polymerization and considered by using numerous method of the techniques. The resulting SrWO4/PEDOT-PPy nanocomposite demonstrated remarkable electrochemical sensing capabilities for sulfadiazine (SFA). As a modified glassy carbon electrode (SrWO4/PEDOT-PPy/GCE) revealed for superior catalytic activity in the electrochemical oxidation of sulfadiazine, enabling sensitive detection with quantification and detection limits of 1.0936 × 10−9 M µA−1 and 2.2104 × 10−9 M µA−1, respectively. This technique effectively determined SFA content in real samples. Additionally, SrWO4/PEDOT-PPy demonstrated extraordinary photocatalytic ability, achieving a Methylene Blue (MB) degradation rate of up to 99.1% under halogen light irradiation within 80 min. Hybrid photocatalyst has exhibited to strong reusability and photocatalytic stability under frequent light exposure. A contrivance for the photocatalytic deprivation of MB by SrWO4/PEDOT-PPy is proposed. These results underscore the crucial role of SrWO4/PEDOT-PPy in practical environmental remediation analysis. The fluorescence investigations have betrothed to terephthalic acid radical formations of SrWO4/PEDOT-PPy hybrids, which were modulated by different approaches, and its mainly driven for higher illumination aptitudes. Meanwhile, this was more supporting for physio-chemical properties of the phenomenon, at this consequential with significantly well improved to the photocatalytic performances. Because of this, SrWO4/PEDOT-PPy hybrid materials were comprehended to deliver excellent kinetics, and better recyclable activities. [ABSTRACT FROM AUTHOR]

ABSTRACT A novel series of pyrimidine sulfonamide derivatives was synthesized through a strategic approach involving the creation of substituted dihydropyrimidinyl‐benzenesulfonamides and subsequent transformation into their chlorinated analogues. These compounds were then subjected to reactions with various amines and phenols, yielding unique substituted sulfapyrimidines. These novel structures integrated essential pharmacophores such as phenols, secondary amines, and benzenesulfonamide moieties, each contributing distinct biological potencies, chemical reactivity, and enhanced pharmacological features. In the pursuit of effective anticancer agents, the newly substituted pyrimidine sulfonamides were characterized using spectroscopic and x‐ray diffraction techniques. The compounds were evaluated for their anti‐proliferative potency against the NCI 60‐cell lines panel, revealing that compound 7c exhibited significant growth inhibition across multiple cancer cell lines. Further assessment through MTT assay on HCT‐116 and MCF‐7 cell lines demonstrated cytotoxicity, while cell cycle analysis of MCF‐7 cells treated with compound 7c revealed arrest at the S phase. Moreover, the effect of 7c on programmed cell death was evaluated using the Annexin V/PI apoptosis assay. The observed promising activity positions these pyrimidine‐based scaffolds as potential candidates for future drug development, offering valuable insights for medicinal chemists engaged in the design and synthesis of anticancer drugs. [ABSTRACT FROM AUTHOR]

Nano TiO2 is an acclaimed photocatalyst, widely used in water treatment due to its remarkable performance. However, challenges in real production, such as the easy recombination of photogenerated carriers and recycling difficulties, limit its application. Heterojunction photocatalysts, with high efficiency of photogenerated carrier separation and large light absorption range, show great potential for efficient water pollution treatment. In this paper, a composite photocatalyst (ART-550) with a heterophase junction structure was developed using industrial submicron rutile TiO2 pigment as the carrier. This composite demonstrated excellent performance in the photocatalytic degradation of sulfadiazine, maintaining its performance over five cycles. Furthermore, it effectively degraded various representative organic pollutants present in water bodies. The construction of a heterophase junction boosted the efficient separation of photo-generated carriers, enabling more active species to participate in the reaction and thus enhancing the photocatalytic degradation performance. Additionally, the strong interfacial binding ensured the stability of the photocatalytic performance of ART-550. This research introduces a new strategy to broaden the application field of submicron rutile and produce nano-titanium dioxide catalysts that are easily accessible, scalable, and highly applicable. It offers promising prospects for advancing water treatment technologies. Highlights: Applying pigment rutile TiO2 in the field of photocatalysis. The highest photocatalytic performance occurred with a 15.7% ratio of the anatase phase. ART-550 demonstrates excellent performance in photocatalytic degradation and is easily recyclable. Sulfadiazine degradation route and photocatalytic mechanism predicted. [ABSTRACT FROM AUTHOR]

Plant macroevolutionary studies leverage the phylogenetic position of non-flowering model systems like the liverwort Marchantia polymorpha to investigate the origin and evolution of key plant processes. To date, most molecular genetic studies in Marchantia rely on hygromycin and/or chlorsulfuron herbicide resistance markers for the selection of stable transformants. Here, we used a sulfonamide-resistant dihydropteroate synthase (DHPS) gene to enable sulfadiazine-based transformation selection in M. polymorpha. We demonstrate the reliability of sulfadiazine selection on its own and in combination with existing hygromycin and chlorsulfuron selection schemes through transgene stacking experiments. The utility of this system is further demonstrated through confocal microscopy of a triple transgenic line carrying fluorescent proteins labelling the plasma membrane, cortical microtubules, and the nucleus. Collectively, our findings and resources broaden the capacity to genetically manipulate the increasingly popular model liverwort M. polymorpha. [ABSTRACT FROM AUTHOR]

The equilibrium solubility of sulfadiazine (SD, 3) in several {acetonitrile (MeCN) + ethanol (EtOH)} mixtures at nine temperatures from T/K = (278.15 K to 318.15) has been determined by following the shake flask method. SD solubility increased with temperature-arising as well as with the MeCN proportion-increasing in the mixtures. Thus, x3 increased from 7.74 × 10−5 in neat EtOH to 6.20 × 10−4 in neat MeCN at T/K = 298.15. SD solubility was adequately correlated with a second-order multivariate equation as function of both mixtures composition and temperature. Moreover, two models including the Jouyban–Acree and Jouyban–Acree–van't Hoff models were applied to mathematical SD solubility data modeling in solvent mixtures. The accuracy of each model is investigated by the mean relative deviations (MRD%) of the back-calculated solubility. A full predictive model was provided by training the Jouyban–Acree–van't Hoff model with only seven experimental solubility data which provided excellent predictions with the MRD% of 3.7 %. All used models show a low MRD% values (< 4.0 %) for the calculated data indicating a good correlation of SD solubility data with the given mathematical models. By means of the van't Hoff and Gibbs equations, the apparent thermodynamic quantities relative to SD dissolution and mixing processes, namely Gibbs energies, enthalpies, and entropies, were calculated and reported. Apparent dissolution quantities of SD were positive in all cases indicating endothermic and entropy-driven behaviors. A non-linear enthalpy–entropy relationship was observed for SD in the plot of SD dissolution enthalpy vs. Gibbs energy. Observed trend exhibits negative slope in the composition from neat EtOH to the mixture of 0.05 in mass fraction of MeCN indicating entropy-driving mechanism for this SD transfer process. Moreover, variant but positive slopes were found in the composition interval of 0.05 < w1 < 1.00 indicating enthalpy-driving mechanism for these SD transfer processes. Furthermore, the preferential solvation of SD by MeCN or EtOH was analyzed by using the inverse Kirkwood–Buff integrals. Thus, SD is preferentially solvated by EtOH molecules in EtOH-rich mixtures but preferentially solvated by MeCN in MeCN-rich mixtures. In this way, this research expands the literature investigations about the solubility of SD in some non-aqueous cosolvent mixtures conformed by MeCN and other alcohols. [ABSTRACT FROM AUTHOR]

[Display omitted] Herein, a novel copper selenide/zinc selenide/Nitrogen-doped carbon (Cu 2 Se/ZnSe/NC) sphere was constructed via a combination of cation exchange, selenization and carbonization approaches with zinc-based metal–organic frameworks (ZIF-8) as precursor for sulfadiazine (SDZ) removal. Compared with the ZnSe/NC, the defective Cu 2 Se/ZnSe interface in the optimizing Cu-ZnSe/NC2 sample caused a remarkably improved adsorption performance. Notably, the adsorption capacity of 129.32 mg/g was better than that of mostly reported adsorbents for SDZ. And the adsorption referred to multiple-layer physical–chemical process that was spontaneous and exothermic. Besides, the Cu-ZnSe/NC2 displayed fast adsorption equilibrium of about 20 min and significant anti-interference ability for inorganic ions. Specially, the adsorbent possessed excellent stability and reusability, which could also be applied for rhodamine B (RhB), methylene blue (MB), and methyl orange (MO) dyes removal. Ultimately, the charge redistribution of Cu 2 Se/ZnSe interface greatly contributes the superior adsorption performance for SDZ, in which electrostatic attraction occupied extremely crucial status as compared to π-π electron-donor–acceptor (π-π EDA) interaction and hydrogen bonding (H-bonding), as revealed by the density function theory (DFT) calculations and experimental results. This study can provide a guideline for design of high-efficient adsorbent with interfacial charge redistribution. [ABSTRACT FROM AUTHOR]

Sulfonamide antibiotics (SAs) widely used have potentially negative effects on human beings and ecosystems. Adsorption and advanced oxidation methods have been extensively applied in SAs wastewater treatment. In this study, compared with Al3+@BC500 and Fe3+@BC500, La3+@BC500 for activating persulfate (S 2 O 8 2−) had the best effect removal performance of sulfadiazine (SDZ) and sulfamethoxazole (SMX). Morphology, acidity, oxygen-containing functional groups, and loading of La3+@BC500 were analyzed by techniques, including EA, BET, XRD, XPS, FT-IR. XRD results show that with the increase of La3+ loading, the surface characteristics of biochar gradually changed from CaCO 3 to LaCO 3 OH. Through EPR technology, it is proved that LaCO 3 OH on the surface of La3+@BC500 can not only activate S 2 O 8 2− to generate SO 4 −•, but also to produce •OH. In the optimization experiment, the optimal dosage of La3+ is between 0.05 and 0.2 (mol/L)/g. SDZ had a good removal effect at pH (5–9), but SMX had a good removal effect only at pH=3. Zeta potential also proves that the material is more stable under acidic conditions. The removal process of SDZ is more in accord with pseudo-first-order kinetics (R 2=0.9869), while SMX is more in line with pseudo-second order kinetics (R 2=0.9926). [Display omitted] [ABSTRACT FROM AUTHOR]

Sulfadiazine (SDZ) is a commonly used antibiotic in medicine, aquaculture, and animal husbandry. However, its misuse has resulted in its release into soil and water environments, posing a gradual threat to the environment and human health. In this study, cotton pulp, poplar sawdust, and corn stover were chosen as raw materials. Zinc chloride (ZnCl2) was used as a modifier to prepare modified porous carbon through pyrolysis at different carbonization temperatures (400 and 800°C). The objective was to investigate the adsorption effect and mechanism of modified porous carbon on SDZ in aqueous environments, as well as the effect of different biomass fractions of the carbon source on the adsorption effect. The physical and chemical properties of the modified porous carbon were characterized by various means of characterization, and the results showed that the high temperature and modification effects made the adsorbent material possess a larger specific surface area and richer pore structure, higher aromaticity, higher degree of graphitization, etc., which would be beneficial for the adsorption of SDZ. Among them, CCPZ800 showed the highest saturation adsorption of SDZ, Q max = 425.45 mg/g. The adsorption experiments were carried out by changing the initial conditions and fitted with kinetic and isothermal adsorption to further explain the adsorption mechanism of modified porous carbon on SDZ in conjunction with the adsorption of SDZ by hydrothermal carbon materials. The results showed that the adsorption of modified porous carbon on SDZ conformed to the quasi-secondary kinetic and Freundlich isothermal adsorption models. Adsorption mechanism of SDZ on modified porous carbon followed a multimolecular layer adsorption, with chemical adsorption being the dominant process. Both physical adsorption and chemical adsorption occurred simultaneously, with the main adsorption mechanism being π–π conjugation. In addition, compositional distribution of biomass from different carbon sources results in variations in pyrolysis mode and pyrolysis products, which in turn affect adsorption. By analyzing the effect of variability in the composition of biomass on the adsorption effect of SDZ, it can be concluded that higher cellulose content in the carbon source leads to a better adsorption effect of SDZ. The study showcases the effectiveness of ZnCl2-modified porous carbon in removing SDZ from water, offering insights into the selection of raw materials for this adsorbent preparation.

In this study, magnetic coconut shell biochar loaded with spherical Fe3O4 and γ-Fe2O3 particles was successfully synthesized using a chemical coprecipitation method. The magnetic biochar exhibited a good magnetic separability and environmental security. The maximum sulfadiazine (SDZ) and norfloxacin (NOR) removal efficiencies were 94.8% and 92.3% at pH 4 and 25 °C with adsorbent dosage of 2.5 g/L, respectively. When antibiotic concentrations ranged from 5 to 50 mg/L, the theoretical maximum adsorption capacities of SDZ and NOR were 16.7 mg/g and 25.8 mg/g, respectively. The Langmuir isotherm and pseudo-second-order kinetic models could better describe the adsorption process of both antibiotics, implying the monolayer chemical adsorption. The thermodynamic analysis indicated that the adsorption process was spontaneous and endothermic. The ionic strength had no significant effect on the adsorption behavior of either antibiotic. Combined with BET, FTIR, and XPS results, the dominant mechanisms for SDZ and NOR adsorption were pore filling, π-π electron-donor–acceptor interaction, hydrogen bonds and surface complexation. Moreover, Lewis acid–base interaction also contributed to SDZ adsorption. [ABSTRACT FROM AUTHOR]

A copper/polydimethylsiloxane (Cu/PDMS) microfluidic chip was designed to synthesize SERS substrates through a displacement reaction between silver and copper in microfluidic channels to form a microfluidic SERS nanoparticles (AgNPs)/Cu chip. This SERS substrate fabrication method doesn't require complex manufacturing processes or expensive equipment, and it can be achieved at room temperature in just 4 min. Meanwhile, the AgNPs grown on copper foil could offer ample hot spots, effectively boosting Raman signals of target molecules, and the enhancement factor (EF) was 5.12 × 107 for methylene blue, 4.08 × 107 for crystal violet, and 4.81 × 105 for sulfadiazine. The chip could be reused at least 9 times with consistent signal performance. Combined with the concentration gradient microchannel network design, we could establish the standard curve for samples through one injection on a single chip. A rapid SERS method for detecting sulfadiazine in aquatic products was developed. The linear range for sulfadiazine analysis was 75.0–1000 μg L−1 with a limit of detection of 28.4 μg L−1. Sulfadiazine was found in aquatic products (43.8 μg kg−1), with recovery rates ranging from 82.7% to 110%. The result was validated using high-performance liquid chromatography, showing a relative error of 9.3%. The entire detection procedure could be completed in just 20 min to detect sulfadiazine. These results demonstrate that the developed SERS method is fast, accurate, and reliable for analysis of sulfadiazine in aquatic products. [ABSTRACT FROM AUTHOR]

The present work concentrates on synthesizing and adsorption surface investigation of polytetrazole polymer (P-T) created from polyimine (P-S) grafted with sulfadiazine drug. The prepared polymer is synthesized by mechanochemical polycondensation reaction between dialdehyde aromatic compound and diamine aromatic compound by applying appropriate polar solvent and glacial acetic acid at (78 °C) as dependent on the polymerization reaction. The synthetic route to prepare tetrazole polymer (P-T) consists off multi chemical reaction process, firstly the synthesis of polyimine backbone (P-S) (4-(((4'-amino-3,3'-dimethyl-[1,1'-biphenyl]-4- yl)imino)methyl)benzaldehyde) by Schiff base reaction between monomers diamine (o-tolidine) and dialdehyde (terephthalaldehyde). Secondly, is the sulfadiazine azid formation, since the conversion of sulfadiazine drug to sulfadiazine azid (4-azido-N-(pyrimidin-2-yl)benzenesulfonamide) occurred by diazonium salt formation of sulfadiazine at very low temperature (0–5 °C) and then reaction with sodium azide (NaN3) under cool conditions to convert amine group (NH2) to azide group (N3), after that sulfadiazine azide was grafted onto the polyimine backbone (P-S) by cyclization reaction process to form polytetrazole (P-T). All prepared products: sulfadiazine azide, polyimine (P-S) and polytetrazole (P-T) were characterized by FT-IR spectroscopy. Finally, the adsorption surface investigations of the prepared polymers (P-S) and (P-T) were studied for adsorption of Brilliant cresyl blue (BCB) dye. All adsorption results were recorded by using an UV-Vis spectrophotometer. Since the polytetrazole (P-T) gave very good adsorption results when applied to (BCB) dye adsorption, there can be suggestion on the polytertazole polymer applicability in many various environmental and medical applications. [ABSTRACT FROM AUTHOR]

Sulfadiazine (SFZ) is an inexpensive large‐consumption antibiotic used for treat bacterial infections but an excess of residues in food can be harmful. Fast and specific luminescence detection of SFZ is highly challenging because of the interference of structurally similar antibiotics. In this work, we develop a two‐dimensional europium‐organic coordination polymer with excellent luminescence and water stability for highly specific detection of SFZ in the range of 0–0.2 mM. Structural analysis shows that the high stability of coordination polymer is due to the high coordination number of europium ion and the special chelating coordination structure of ligand. The experiment results revealed that the high selectivity and effectively luminescence quenched behaviour of coordination polymer toward SFZ is caused by highly efficient inner filter effect. [ABSTRACT FROM AUTHOR]

Gold nanoparticles (AuNPs) were extensively employed for in-situ detection sulfadiazine (SDZ) residues, yet current synthesis methods suffer from complex procedures, reagent pollution of the environment, and low particle quality. This study presents a novel synthesis method using discarded longan seed extract as a reducing agent to synthesized high-quality AuNPs, and then can be used for in-situ SDZ detection. Response surface methodology (RSM) was employed to optimize synthesis parameters, which resulted in five optimal combinations that enhanced the flexibility of synthesis. These AuNPs, ranging in size from 18.26 nm to 33.8 nm with zeta potentials from − 29.5 mV to − 14.3 mV, were successfully loaded with functional groups from longan seed extract. In the detection of SDZ, the colorimetric aptasensor demonstrated excellent sensitivity and selectivity over other antibiotics with a limit of detection and quantification at 70.98 ng·mL−1 and 236.59 ng·mL−1 in the concentration range of 200–800 ng·mL−1. Recoveries of spiked SDZ samples ranged from 97.90% to 106.7%, with RSD values below 9.25%. Meanwhile, the aptasensor exhibited exceptional diagnostic efficacy (AUC: 0.976) compared to UV absorption methods in the ROC evaluation. In conclusion, this study highlights the potential of using AuNPs synthesized from longan seed extract coupled with aptamer technology as a straightforward detection method for SDZ in river water, offering promising applications in environmental monitoring. [ABSTRACT FROM AUTHOR]

A tumor-targeting fluorescent probe has attracted increasing interest in fluorescent imaging for the noninvasive detection of cancers in recent years. Sulfonamide-containing naphthalimide derivatives (SN-2NI, SD-NI) were synthesized by the incorporation of N-butyl-4-ethyldiamino-1,8-naphthalene imide (NI) into sulfonamide (SN) and sulfadiazine (SD) as the tumor-targeting groups, respectively. These derivatives were further characterized by mass spectrometry (MS), nuclear magnetic resonance spectroscopy (1H NMR), Fourier transform infrared spectroscopy (FT-IR), ultraviolet–visible spectroscopy (UV), and a fluorescence assay. In vitro properties, including cell cytotoxicity and the cell uptake of tumor cells, were also evaluated. Sulfonamide-containing naphthalimide derivatives possessed low cell cytotoxicity to B16F10 melanoma cells. Moreover, SN-2NI and SD-NI can be taken up highly by B16F10 cells and then achieve good green fluorescent images in B16F10 cells. Therefore, sulfonamide-containing naphthalimide derivatives can be considered to be the potential probes used to target fluorescent imaging in tumors. [ABSTRACT FROM AUTHOR]

The widespread use of antibiotics like sulfadiazine (SDZ) in various industries has raised environmental and health concerns due to their potential for bioaccumulation and the subsequent effects on human health and the environment. Diethylcarbamazine citrate (DCZ), a well‐established antifilarial drug, has yet to be explored as a sensing agent despite its extensive use. This study proposes a cost‐effective and efficient method for detecting SDZ and Uric acid (UA) using a DCZ‐modified carbon paste electrode (poly‐DCZ/MCPE). The poly‐DCZ film is synthesized via cyclic voltammetry (CV) on the carbon paste electrode surface, demonstrating excellent electrocatalytic activity for SDZ and UA detection at pH 7.4. The diffusion‐controlled electrode process is observed with a lower limit of detection (LOD) and limit of quantification (LOQ) for SDZ as 3.8×10−9 M and 12.94×10−9 M respectively. For UA, LOD and LOQ were found to be 6.291×10−9 M and 20.97×10−9 M respectively at the poly‐DCZ/MCPE. Notably, the sensor exhibits simultaneous detection capabilities for SDZ and UA by CV and differential pulse voltammetry (DPV) methods, addressing the need to monitor antibiotic residues in aquatic ecosystems and animal‐derived products. [ABSTRACT FROM AUTHOR]

The impact of antibiotic residue on sediment ecology at the watershed level is not yet fully understood. In this investigation, varying concentrations of oxytetracycline (OTC) and sulfadiazine (SD) were added to the overlying water of both the upper (0–10 cm) and bottom sediment (20–30 cm) layers at the watershed scale to evaluate the ecological impact on sediment habitats through the analysis of the activities of enzymes, namely urease (UA), alkaline phosphatase (APA), peroxidase (POA), and dehydrogenase (DHA). Results showed that the levels of UA and APA in the bottom sediment layers exceeded those in the top sediment layer upon reintroduction of antibiotics. Conversely, the fluctuations in DHA were notably reduced across various types of antibiotics and exposure concentrations in the bottom sediment layers. Within the top sediment layers, as the concentration of OTC exposure increased, there was a corresponding elevation in POA levels. However, the response of POA initially ascended and subsequently descended with rising SD exposure concentration, although it consistently exceeded the control levels. In contrast, the response of DHA displayed an inverse correlation with OTC exposure concentration but a direct correlation with SD exposure concentration. At the watershed scale, under antibiotic exposure, UA and DHA exhibited significantly higher levels upstream compared to downstream. Conversely, APA and POA appeared relatively stable across the watershed following the reintroduction of antibiotics. Moreover, DHA demonstrated a noticeable decreasing trend with increasing concentrations of OTC exposure. Environmental factors had a predominant influence, exceeding 40%, on enzyme activities during antibiotic reintroduction. Specifically, particle size significantly inhibited enzyme activity, while sediment nutrient conditions, including total carbon, nitrogen, and sulfur content, significantly enhanced enzyme activities. The study suggests that enzyme activities associated with antibiotic reintroduction in watershed sediments are established during stable stages in the bottom sediment layer or downstream sediment environment as part of sedimentary and transport processes. More research is required to explore the maintenance and evolution of antibiotic resistance profiles in the presence of long-term antibiotic residues. [ABSTRACT FROM AUTHOR]

Production and evaluation of the kinetic stability of the amorphous forms of active pharmaceutical ingredients are among the current challenges of modern pharmaceutical science. In the present work, amorphous forms of several sulfonamides were produced for the first time using Fast Scanning calorimetry. The parameters, characterizing the glass-forming ability of the compounds, i.e. the critical cooling rate of the melt and the kinetic fragility, were determined. The cold crystallization kinetics was studied using both isothermal and non-isothermal approaches. The results of the present study will contribute to the development of approaches for producing amorphous forms of rapidly crystallizing active pharmaceutical ingredients. [Display omitted] • The key parameters characterizing the glass-forming ability of these rapidly crystallizing sulfonamides were determined for the first time. • The critical cooling rates were found to be 3 K/s for sulfamethoxazole, 350 K/s for sulfamerazine, and 2000 K/s for sulfadiazine. • The kinetic fragility values of the sulfadiazine, sulfamerazine and sulfamethoxazole are 44, 38 and 40. • The best agreement between the predictions based on the non-isothermal kinetic data and the experimental isothermal crystallization halftimes was achieved based on the Nakamura crystallization model. [ABSTRACT FROM AUTHOR]

OBJECTIVE To investigate the role of curcumin in the regulation of P-glycoprotein (P-gp) and its influence on the pharmacokinetics of P-gp substrates. SAMPLE 39 broiler chicken and chicken embryonic primary hepatocytes. METHODS Chicken embryonic primary hepatocytes were treated with curcumin, after which cell viability, P-gp expression, and transport were assessed. Broiler chickens were pretreated with curcumin, after which P-gp expression and the pharmacokinetic behavior of orally administered sulfadiazine (a substrate of P-gp) were measured. RESULTS The preliminary results showed that the viability of chicken embryonic primary hepatocytes was enhanced by pretreatment with 40, 60, and 100 μM curcumin. Curcumin inhibits the expression and transport of P-gp. In vivo experiments showed that curcumin decreased the expression of P-gp in the broiler chicken liver, kidney, and small intestine. Pretreatment with curcumin changed the pharmacokinetic behavior of orally administered sulfadiazine by increasing the area under the curve (47.36 vs 70.35 h·mg/L, P < .01) and peak concentration (10.1 vs 14.53 μg/mL, P < .01). CLINICAL RELEVANCE Curcumin inhibited the expression and efflux of chicken P-gp, thereby improving the oral bioavailability of P-gp substrate drugs. These findings provide a rationale for exploiting herbal-drug interactions in veterinary practice to improve the absorption of drugs. [ABSTRACT FROM AUTHOR]

Heterogeneous catalyst-mediated sulfate radical-based advanced oxidation processes (SR-AOPs) showed excellent performance during antibiotics degradation. Spinel was a promising catalyst for SR-AOPs, but the secondary contamination due to metal ions leaching needed to be addressed. And the destruction of catalyst structure could lead to the reduction of catalytic activity and the difficulty of recovery. Thus, a novel nitrogen-doped carbon (NC)-supported CoFe2O4 (CoFe2O4@NC) was synthesized as the activator of PMS for sulfadiazine (SDZ) degradation under low Co leaching conditions. The consequences indicated that the CoFe2O4@NC/PMS system exhibited higher PMS decomposition efficiency and reaction stoichiometry efficiency than the bare CoFe2O4/PMS systems (CoFe2O4-180 and CoFe2O4-800), which in turn demonstrated a better SDZ removal performance. Under the condition of CoFe2O4@NC dosage 0.1 g/L, PMS concentration 0.5 mM, solution pH 6.8 and temperature 25°C, SDZ (20 mg/L) was almost completely degraded within 60 min. XPS analysis showed that the NC not only protected and stabilized CoFe2O4, but also provided additional active sites for PMS activation. During SDZ degradation, SO4•−, HO•, •O2− and 1O2 were involved in the reaction, among which SO4• and HO• made the main contribution. Meanwhile, CoFe2O4@NC could be recovered by magnetic separation, and showed great stability (Co leaching 0.852 mg/L) and reusability. In the fifth cycle experiment, 85.02 % SDZ degradation was obtained. Based on the detected intermediates (12 intermediates were identified) and DFT calculations, possible degradation pathways for SDZ in CoFe2O4@NC/PMS were proposed. The condensed dual descriptor indicated that the N7, N11, and C15 atoms on SDZ molecule were the main sites of electrophilic attack, which was consistent with the detected intermediates. The degradation of SDZ involved hydroxylation of NH2, cleavage of S−N and extrusion of SO2. This study explored the improvements made in NC support material to catalytic performance and resistance to dissolution of spinel, providing new insights for subsequent researches.

Piezocatalysis, a heterogeneous catalytic technique, leverages the periodic electric field changes generated by piezoelectric materials under external forces to drive carriers for the advanced oxidation of organic pollutants. Antibiotics, as emerging trace organic pollutants in water sources, pose a potential threat to animals and drinking water safety. Thus, piezoelectric catalysis can be used to degrade trace organic pollutants in water. In this work, BaTiO3 and La-doped BaTiO3 were synthesized using an improved sol–gel–hydrothermal method and used as piezocatalytic materials to degrade sulfadiazine (SDZ) with ultrasound activation. High-crystallinity products with nano cubic and spherical morphologies were successfully synthesized. An initial concentration of SDZ ranging from 1 to 10 mg/L, a catalysis dosage range from 1 to 2.5 mg/mL, pH, and the background ions in the water were considered as influencing factors and tested. The reaction rate constant was 0.0378 min−1 under the optimum working conditions, and the degradation efficiency achieved was 89.06% in 60 min. La-doped BaTiO3 had a better degradation efficiency, at 14.98% on average, compared to undoped BaTiO3. Further investigations into scavengers revealed a partially piezocatalytic process for the degradation of SDZ. In summary, our work provides an idea for green environmental protection in dealing with new types of environmental pollution. [ABSTRACT FROM AUTHOR]

The Schiff base was synthesized and characterized with Infrared, Raman, UV, fluorescence, and NMR studies. The present work is theoretically investigated using DFT/WB97XD/cc-pVTZ basis set. The local energy decomposition (LED) has been performed using PBE0-D3/deft-TZVP basis set and DLPNO-CCSD(T) coupled cluster level. The DFT was used to define the molecular structure and geometry of the compound. To identify the primary binding sites and weak interactions, compound was subjected to a series of topological analyses, including ELF, LOL, ALIE, and RDG. The UV-Visible spectrum was analyzed using the TD-SCF method. The DFT/WB97XD/cc-pVTZ was used to measure the HOMO-LUMO, MEP, and NLO. The NBO calculations investigate the intermolecular and intramolecular movement of charges, as well as the molecule stability. To determine whether the 4CLBDA molecule has the potential to become a drug, computational drug-likeness studies were conducted. The docking study done against the 6X7Q protein is performed and reported. [ABSTRACT FROM AUTHOR]

This work is focused on the development of a sensitive voltammetric electrode for sulfadiazine using nanoparticles of Tb2(WO4)3 to modify a carbon paste electrode (CPE). The behavior of the modified CPE was evaluated through cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and fast Fourier transform square wave voltammetry (FFTSWV). The results revealed an irreversible sulfadiazine oxidation peak around 0.85 V vs. the Ag/AgCl reference electrode. The physicochemical properties of the nano-material were investigated using scanning electron microscopy (SEM), and X-ray powder diffraction (XRD). Some effective parameters such as, pH, percentage of modifier, amplitude, and frequency on sensor sensitivity were studied and optimized. The analytical curve was then obtained in the concentration ranges of 0.01-1.0 μM and 1.0-100 μM (with different sensitivity) with a detection limit of 4.10 nM by fast Fourier transform square wave voltammetry. Also, the electron transfer coefficient (α) was determined as a value of 0.66 for the sulfadiazine oxidation. The drug analysis in the pharmaceutical formulation was also carried out and recovery percentages in the range of 97-102% were recorded. The sensor presented good reproducibility and repeatability with acceptable RSD values (3.8%, 1.02% respectively) and long-term stability (almost one month). [ABSTRACT FROM AUTHOR]

Antibiotic contamination in soil has become a major concern worldwide. At present, it is not clear how two co-existed antibiotics with environmentally relevant concentrations would affect soil bacterial community structure, the abundances of antibiotic resistance genes (ARGs) and functional genes, and whether the effects of antibiotics would differ between rhizosphere and bulk soil. We conducted a greenhouse pot experiment to grow maize in a loess soil treated with oxytetracycline (OTC) or sulfadiazine (SDZ) or both at an environmentally relevant concentration (1 mg kg−1) to investigate the effects of OTC and SDZ on the rhizosphere and bulk soil bacterial communities, abundances of ARGs and carbon (C)-, nitrogen (N)-, and phosphorus (P)-cycling functional genes, and on plant growth and plant N and P nutrition. The results show that the effects of environmentally relevant concentrations of OTC and SDZ on bacterial communities and abundances of ARGs and functional genes differ between maize rhizosphere and bulk soil. The effects of two antibiotics resulted in a higher absolute abundances of accA, tet(34), tnpA-04, and sul2 in the rhizosphere soil than in the bulk soil and different bacterial community compositions and biomarkers in the rhizosphere soil and the bulk soil. However, OTC had a stronger inhibitory effect on the abundances of a few functional genes in the bulk soil than SDZ did, and their combination had no synergistic effect on plant growth, ARGs, and functional genes. The role of co-existed OTC and SDZ decreased shoot height and increased root N concentration. The results demonstrate that environmentally relevant concentrations of antibiotics shift soil microbial community structure, increase the abundances of ARGs, and reduce the abundances of functional genes. Furthermore, soil contamination with antibiotics can diminish agricultural production via phytotoxic effects on crops, and combined effects of antibiotics on plant growth and nutrient uptake should be considered. [ABSTRACT FROM AUTHOR]

Background: Burns are a serious public health problem worldwide, causing high morbidity and mortality. This study aimed to compare two forms of treatment for partial skin burns and to determine whether one is superior to the other in terms of efficacy and benefits through a meta-analysis of randomized controlled trials. This article highlights the efficacy of tilapia skin in the treatment of burns. We performed a meta-analysis of 199 patients and highlighted the promising results that indicate the clinical relevance of this resource when we compared the cost of dressings with the daily need for dressing changes, healing potential, and reduction in pain level according to the VAS scale and reduced frequency of dressing changes. Methods: A search of PubMed, Cochrane Central, and LILACS was performed to identify randomized controlled trials comparing tilapia skin and silver-based dressings for treating burns. Studies involving overlapping populations and animals were excluded. The outcomes of interest were complete re-epithelialization, decreased pain level, and dressing change. Results: Summarize the article's main findings. Conclusions: Four randomized trials were included with a total of 199 patients with partial-thickness burns between the ages of 2 and 70 years. A total of 99 (49.74%) patients were treated with tilapia skin, and conventional treatment was used on 100 (50.25%) of the patients. Differences were found between the tilapia and silver-based treatments concerning re-epithelialization (MD −0.48; CI 95% −0.71 to −0.24; p < 0.01; I2 = 0%), decreased pain level (MD −0.79; CI 95% −1.10 to −0.47; p < 0.01; I2 = 0%), and dressing change outcome (MD −3.54; 95% CI −5.81 to −1.26; p = 0.02; I2 = 97%). [ABSTRACT FROM AUTHOR]

A new class of (N‐(pyrimidin‐2‐yl)‐4‐((1,7,7‐trimethylbicyclo [2.2.1] heptan‐2‐ylidene) amino) benzenesulfonamide (CDA) was synthesized from commercially available camphor and sulfadiazine. The synthesized Schiff‐base was characterized by FT‐IR, 1H and 13C NMR spectroscopic analyses. The HOMO, LUMO, MEP, chemical reactivity parameters, and NBO were calculated using the WB97XD/cc‐pVDZ basis set. For better understanding, the electronic absorption and emission of the compound were recorded using UV‐Vis and fluorescence spectra. Molecular docking simulations were investigated between ligand (compound) and target protein. The computational results correlate well with observed values. The frontier molecular orbital energy gap (3.78 eV) revealed that the studied molecule has higher polarizability and chemical reactivity with lower kinetic stability. In addition, compound showed the highest binding score −5.72 kcal/mol, which was confirmed by a molecular docking simulation. [ABSTRACT FROM AUTHOR]

The simple, economic, and conventional diazo-coupling method was developed for the synthesis of five different scaffolds of sulfadiazine incorporated azo dyes in acidic medium at chilled condition. The structural aspects of the prepared azo dyes were confirmed by various physical and spectroscopic techniques such as elemental analysis, electronic absorption studies, infrared, nuclear magnetic resonance (1H and 13C), and mass spectrometry. The electronic absorption study indicates that all the prepared azo dyes possess excellent coloring properties and it is supported by its molar absorptivity values. Further, these azo colorants were examined for different biological studies such as antimicrobial assay, radical scavenging, antituberculosis, anti-inflammatory, and DNA cleavage studies. From the results, all the studied azo dyes showed provoked and proficient biological efficacy against the tested assays. [ABSTRACT FROM AUTHOR]

Monomeric [Co(SDZ)2phen] (1) and [Co(SDZ)(bq)Cl] (2) complexes (SDZ = sulfadiazine, phen = 1,10-phenanthroline, and bq = 2,2′-biquinoline) have been synthesized and characterized. X-ray diffraction studies indicate that SDZ acts as a bidentate ligand coordinating through the sulfonamide and the pyrimidine N atoms in both compounds. In complex 1, the coordination sphere consists of two SDZ ligands and a bis-chelating phen ligand, giving rise to a CoN6 coordination sphere. On the other hand, 2 has a CoN4Cl core, with two N-atoms from SDZ and two from the bq ligand. Both compounds have been studied by dc and ac magnetometry and shown to display slow magnetic relaxation under an optimum external dc field (1 kOe) at low temperatures. Moreover, compound 2 displays long range magnetic ordering provided by spin-canted antiferromagnetism, which has been characterized by further field-dependent magnetic susceptibility measurements, FC/ZFC curves, hysteresis loops and frequency-independent ac curves. The signs of the calculated D parameters, positive in 1 and negative in 2, have been rationalized according to the two lowest-lying transitions in the orbital energy diagrams derived from ab initio ligand field theory (AILFT). In a subsequent attempt to reveal the possible hidden zero-field SMM behaviour, Ni(II)-based 3 and Co(II)-doped Ni(II)-based (with a Ni : Co ratio of 0.9 : 0.1) heterometallic compound 2Ni were synthesized. [ABSTRACT FROM AUTHOR]

Drug repurposing is a promising approach that has the potential to revolutionize the drug discovery and development process. By leveraging existing drugs, we can bring new treatments to patients more quickly and affordably. Anti-inflammatory drugs have been shown to target multiple pathways involved in cancer development and progression. This suggests that they may be more effective in treating cancer than drugs that target a single pathway. Cell viability was measured using the MTT assay. The expression of genes related to inflammation (TNFa, IL1b, COX-1, COX-2, and 5-LOX) was measured in HepG2, MCF7, and THLE-2 cells using qPCR. The levels of TNFα, IL1b, COX-1, COX-2, and 5-LOX were also measured in these cells using an ELISA kit. An enzyme binding assay revealed that sulfadiazine expressed weaker inhibitory activity against COX-2 (IC50 = 5.27 μM) in comparison with the COX-2 selective reference inhibitor celecoxib (COX-2 IC50 = 1.94 μM). However, a more balanced inhibitory effect was revealed for sulfadiazine against the COX/LOX pathway with greater affinity towards 5-LOX (IC50 = 19.1 μM) versus COX-1 (IC50 = 18.4 μM) as compared to celecoxib (5-LOX IC50 = 16.7 μM, and COX-1 IC50 = 5.9 μM). MTT assays revealed the IC50 values of 245.69 ± 4.1 µM and 215.68 ± 3.8 µM on HepG2 and MCF7 cell lines, respectively, compared to the standard drug cisplatin (66.92 ± 1.8 µM and 46.83 ± 1.3 µM, respectively). The anti-inflammatory effect of sulfadiazine was also depicted through its effect on the levels of inflammatory markers and inflammation-related genes (TNFα, IL1b, COX-1, COX-2, 5-LOX). Molecular simulation studies revealed key binding interactions that explain the difference in the activity profiles of sulfadiazine compared to celecoxib. The results suggest that sulfadiazine exhibited balanced inhibitory activity against the 5-LOX/COX-1 enzymes compared to the selective COX-2 inhibitor, celecoxib. These findings highlight the potential of sulfadiazine as a potential anticancer agent through balanced inhibitory activity against the COX/LOX pathway and reduction in the expression of inflammatory genes. [ABSTRACT FROM AUTHOR]

In this work, a dual‐emission ratiometric fluorescence sensor was prepared and used for the detection of sulfadiazine (SDZ) drug. The hydrothermal method was used to synthesize carbon quantum dots (CQD) (fluorescence response signal) and sulfhydryl‐modified cadmium telluride quantum dots (fluorescence reference signal), and a molecularly imprinted polymer was subsequently synthesized. After eluting the template molecule SDZ, the blot recognition site remains on the surface of the imprinted polymer. During the process of detection, due to electron transfer between SDZ and CQDs, holes of stimulated electrons are filled. This leads to fluorescence quenching at around 430 nm, which greatly improves sensor selection performance. Compared with traditional single‐emission fluorescence sensors, ratiometric fluorescence sensors have a wider linear range and higher detection accuracy. Under the optimal conditions, the sensor exhibited excellent performance in terms of low detection limit (4.2 nmol L−1) and satisfactory linear range (2–20 μmol L−1). This intelligent response change mode also provides prospect for detection of other sulfonamide antibiotics and offers a reference to signal transform for other molecular imprinting technologies. © 2023 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

Copyright of Environmental Science & Technology (10036504) is the property of Editorial Board of Environmental Science & Technology and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The main goal of this article is to elucidate the SDZ and TN removal characteristics and mechanisms of a saline-resistant strain of Acinetobacter sp. RT-6. The SDZ and TN removal characteristics indicated that SDZ and TN removal were significantly affected by SDZ concentration and salinity. The removal curves and kinetics of different typical amounts of nitrogen showed the shortcut nitrification and denitrification present in the ammonia-N removal process; the nitrogen-containing compound was mainly transformed into N2, and approximately 19.05 ± 0.83 mM of the electrons was transferred to the nitrate respiratory chain. The intermediates of SDZ degradation were identified, and it was speculated that the main reaction sites for SDZ transformation were the N–C bond, N–S bond, pyrimidine ring, and benzene ring. [ABSTRACT FROM AUTHOR]

Antibiotic resistance genes (ARGs) can be easily promoted by antibiotics, however, the structural effects of antibiotics on the proliferation of ARGs dynamic and the associated mechanisms remain obscure in, especially, activated sludge sequencing batch reactors. In the present study, the effects of 9 sulfonamides (SAs) with different structures on the proliferation dynamic of sulfonamide resistance genes (Sul s) in the activated sludge sequencing batch reactors and the corresponding mechanisms were determined (30 days), and the results showed that the largest proliferation value (∆ A R) of Sul s dynamic for SAs (sulfachloropyridazine) was approximately 2.9 times than that of the smallest one (sulfadiazine). The proliferation of Suls was significantly related to the structural features (minHBint6, SssNH, SHBd and SpMax2_Bhm) that represent the biological activity of SAs. To interpret the phenomenon, a mechanistic model was developed and the results indicated that the biodegradation of SAs (T 1/2) rather than conjugative transfer frequency or mutation frequency tends to be the key process for affecting Sul s proliferation. T 1/2 was proved to be dependent on the interactions between SAs and receptors (E binding), the cleavage mode (bond dissociation energy), and the site of nucleophilic assault. Besides, the metagenomic analysis showed that SAs posed significant effect on antibiotic resistome and Tnp31 played a vital role in the proliferation of Suls. Overall, our findings provide important insight into a theoretical basis for understanding the structural effects of SAs on the proliferation of ARGs in SBR systems. [ABSTRACT FROM AUTHOR]

To improve the activation efficiency of PMS to efficiently degrade antibiotic sulfadiazine (SD), herein, a Co@MoS2 catalyst was prepared by a one-step hydrothermal process. The unique petal-like structure of MoS2 enables the transition metal Co to achieve high dispersion and avoid agglomeration. Mo(IV) and unsaturated S accelerate the electron transfer between Co 2 + and Co 3 + to improve the cycling efficiency and thus realize the efficient activation of PMS. The results of active substance quenching experiment and ESR analysis show that the main active substance for the efficient degradation of SD by Co@MoS2 is the non-radical 1O2, while the other three radicals ⋅ O 2 − , ⋅OH and SO 4 • − contribute significantly to the efficient degradation of SD. And after 5 cycles, the degradation could still be as high as 90%. The strong consolidation of Co on the petal-shaped sheet of MoS2 ensures the stability of Co@MoS2 catalyst. Co@MoS2 catalyst was prepared by one-step hydrothermal process. The unique petal-like structure of MoS2 enables the transition metal Co to achieve high dispersion and avoid agglomeration. Mo(IV) and unsaturated S accelerate the electron transfer between Co2+ and Co3+ to improve the cycling efficiency and thus realize the efficient activation of PMS. The main active substance for the efficient degradation of sulfadiazine by Co@MoS2 is the non-radical 1O2, while the other three radicals ⋅ O 2 − , ⋅OH and SO 4 • − contribute significantly to the efficient degradation of sulfadiazine. The strong consolidation of Co on the petal-shaped sheet of MoS2 ensures the stability of Co@MoS2 catalyst. [ABSTRACT FROM AUTHOR]

The eco-friendly techniques were utilized for the straightforward synthesis of new heterocyclic compounds bearing the sulfadiazine moiety by employing ultrasound irradiation techniques. Initially, sulfadiazine (1) was subjected to diazotization, followed by a coupling reaction with an activated methylene group (ethyl acetoacetate) to yield a hydrazone compound (3). Subsequently, the coupling adducts (3) were reacted with ethyl benzoylacetate, benzyl hydrazine, thiosemicarbazide, and guanidine under ultrasound irradiation, leading to the formation of pyridazine (4), pyrazolines (5, 6), and pyrimidine (7), respectively. Furthermore, when pyrazoline compound (6) was treated with chloroacetone and bromoaceophenone under ultrasound conditions, thiazole compounds (6a) and (6b) were formed, respectively. Additionally, new derivatives (10) and (11) were synthesized through diazotizing compound (7), followed by coupling reactions with an activated methylene group (acetylacetone) and reactions with urea and thiourea, respectively, all under ultrasound conditions. All the synthesized compounds were characterized using spectroscopic techniques such as FT IR, ¹H-NMR, and 13C-NMR spectra. The synthesized chemicals exhibited promising antimicrobial activities against human pathogenic bacteria strains (Escherichia coli and Staphylococcus aureus) and Candida albicans fungi, as assessed through the broth microdilution technique. [ABSTRACT FROM AUTHOR]

Magnetite-functionalized biochar (MBC) is a promising engineered material for remediation of antibiotic-contaminated fields. However, sorption mechanisms of ionizable organic compounds such as sulfonamide antibiotics (SAs) on MBC are still unclear. This study employed four representative SAs including sulfamethazine (SMT), sulfamerazine (SMR), sulfadiazine (SDZ), and sulfamethoxazole (SMX), to compare the difference in sorption on MBC. Results showed that the sorption capacities and affinities of the four SAs varied with their substituents, hydrophobic properties, and dissociation constants (pKa). Synergistic effect during co-pyrolysis with Fe3+ enhanced the sorption performance of MBC towards SAs compared to original BC. Spectral methods confirmed structural changes of MBC such as the variance in oxygen-containing groups and defective/graphitized phases. Results of modeling pH-dependent sorption revealed that H-bonding or π-bond assisted H-bonding determined the sorption affinities and capacities of SAs. In particular, the SAs with lower pKa were thermodynamically favorable to form H-bonding with MBC via proton exchange with water molecules. Quantum calculation results quantified the contributions of H-bonding strengths and found that the energies of H-bonding were correlated with affinities of SAs. Moreover, contributions of oxygen-containing groups instead of minerals dominated the H-bonding energies. Mechanistic insights from this study can be valuable in exploring engineered BC composites for practical application in field remediation. Highlights: Sorption capacity and affinity of four SAs varied with substituents, Kow, and pKa Copyrolyzed carbon matrix and Fe3+ synergistically enhanced SA sorption performance H-bonding or π-bond assisted H-bonding determined SA sorption affinity and capacity Contributions of O-containing groups instead of minerals dominated H-bonding energy [ABSTRACT FROM AUTHOR]

Hydrothermal pretreatment (HTP) can be used to decompose the sulfadiazine (SDZ) during continuous anaerobic digestion (AD) of pig manure. This study aims to explore the effect of HTP on the SDZ degradation and performance of AD system. Pig manure with SDZ was taken as the research object. A comparison was made on the degradation regular, SDZ paths and products, as well as the gas production performance of pig manure with/without HTP during AD. The results showed that the HTP (150 °C) significantly increased the comprehensive removal rate of SDZ in the mesophilic continuous AD reactor (P <0.05), particularly from 40.5%~58.5% to 54.4%~75.2%. Moreover, the biodegradation paths of SDZ were inferred through intermediate degradation products, including SDZ hydrolysis, hydroxylation, thiodeoxidation, amino oxidation, nitroation, amidation and pyrimidine ring cleavage. HTP enhanced the degradation products and paths of SDZ, biodegrade SDZ from different degradation paths, and the removal rate of SDZ. There were four paths of degradation in pig manure with HTP, while there was only one degradation path without HTP. In terms of AD performance, the system was stabilized after 25 days, the daily gas production in the R0 reactor was stable at 5.14 L/d, and the cumulative VS gas production rate was 16.64 L/g; In the R0h reactor, the daily gas production was stable at 6.89 L/d, and the cumulative VS gas production rate was 22.31 L/g. The daily biogas yield of the reactor and the volume production rate increased by about 34.05% (P<0.05), and 34.00%, respectively, after stable operation with HTP. There was little difference in the methane content between the two reactors after two SRTs. The average contents of methane in R0 and R0h reactors were 61% and 59%, respectively. Thus, the AD process was stable in the two groups of reactors over the whole operation stage, according to the biogas production rate and methane content. The degradation of organic matter was also enhanced for the high concentration of VFAs after HTP. The substrate was provided for the subsequent stage of methane production, in which the acetic acid content accounted for 25.3%~46.1%. In addition, the microbial communities showed that Firmicutes and Bacteroidota were the dominant phylum bacteria in the reactors during anaerobic fermentation. Their relative abundance was beneficial to the degradation of antibiotics. A comparative analysis was also made on the microbial community at the class level. It was found that Clostridia and Bacteroidia were the main microorganisms in the two reactors. The relative abundance of Proteiniphilum increased after HTP. The full hydrolysis of pig manure was also realized for the better performance of methane production. Meanwhile, it was found that Syntrophomonas and Sedimentibacter were highly correlated with the degradation of SDZ, and the relative abundance of Sedimentibacter after HTP was significantly higher than that without HTP, indicating the better degradation of antibiotics. Therefore, the HTP coupled with the AD process can be expected to simultaneously improve the degradation of SDZ and AD performance, particularly for the ecological safety of biogas liquor. [ABSTRACT FROM AUTHOR]

In this work, two CdII-based coordination polymers, namely [Cd4(HL)2(H2O)5]n (1), and {[Cd2(HL)(2,2′-bpy)2(H2O)]·6H2O}n (2) (2,2′-bpy = 2,2′-bipyridine) have been designed and synthesized using 2,3-bis(3,5-dicarboxylphenxoy)benzoic acid (H5L). Coordination polymer 1 displays a layer structure, which was connected through C–H‧‧‧π interactions into 3D supramolecular network, while coordination polymer 2 shows a three-dimensional framework structure. In addition, the excellent fluorescence performance make them potential luminescent sensors for antibiotics. The results show that coordination polymer 1 exhibits high sensitivity for detecting of sulfadiazine (SDZ), while coordination polymer 2 can selectively detect nitrofurantoin (NFT). [ABSTRACT FROM AUTHOR]

The composite material based on N-, S-, and Fe-doped TiO2 (NSFe-TiO2) synthesized by wet impregnation was used as a photocatalyst to rapidly degrade sulfadiazine. The photocatalytic degradation behavior and mechanism of sulfadiazine on NSFe-TiO2 were investigated for revealing the role of degradation under ultraviolet light. The results showed that compared with TiO2, NSFe-TiO2 markedly improved the efficiency in photocatalytic degradation of sulfadiazine: more than 90% of sulfadiazine could be removed within 120 min by NSFe-TiO2 dosage of 20 mg L−1. The process conformed to first-order reaction kinetics model. The parameters such as loaded amount of NSFe-TiO2, solution pH value, humic acid concentration and recycle numbers on removal efficiency were also studied. Compared to neutral and alkaline conditions, acidic condition was not conducive to the photocatalysis. HA, Ca2+, Cu2+ and Zn2+ in the actual water body had mild inhibition on sulfadiazine degradation in UV/NSFe-TiO2 system. Fragments screened by high-resolution mass spectrometry were conducted to explore the oxidation mechanism and pathways of sulfadiazine degradation. On the whole, UV/NSFe-TiO2 photocatalysis has a good effect on sulfadiazine removal. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Jilin University (Science Edition) / Jilin Daxue Xuebao (Lixue Ban) is the property of Zhongguo Xue shu qi Kan (Guang Pan Ban) Dian zi Za zhi She and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The continuous emergence of food additives and contaminants in edibles, especially confectioneries, demands advanced detection methods to ensure public health and safety. Vanillin (VAL) and sulfadiazine (SD) are of paramount concern due to their extensive application in various products. While VAL is favored for its flavoring attributes, SD, a common antibiotic, can inadvertently contaminate food items. For accurate and swift detection of these compounds, we introduced an innovative electrochemical sensor using cobalt oxide nanostructures. Notably, synthesizing these nanostructures through a green approach using glucose and starch is a significant advancement, offering both environmental benefits and enhanced material properties. The novelty of the material lies in its eco-friendly synthesis route and superior electrocatalytic performance. Preliminary results indicate a promising limit of detection (LOD) VAL= 0.003 µM & SD= 0.0055 µM and a broad linear range 0.02–209 µM emphasizing its potential for real-world food quality monitoring. This work, therefore, provides a crucial intersection of sustainable material synthesis and effective food contaminant detection, heralding a new era in food safety evaluation.

The eco-friendly techniques were utilized for the straightforward synthesis of new heterocyclic compounds bearing the sulfadiazine moiety by employing ultrasound irradiation techniques. Initially, sulfadiazine (1) was subjected to diazotization, followed by a coupling reaction with an activated methylene group (ethyl acetoacetate) to yield a hydrazone compound (3). Subsequently, the coupling adducts (3) were reacted with ethyl benzoylacetate, benzyl hydrazine, thiosemicarbazide, and guanidine under ultrasound irradiation, leading to the formation of pyridazine (4), pyrazolines (5, 6), and pyrimidine (7), respectively. Furthermore, when pyrazoline compound (6) was treated with chloroacetone and bromoaceophenone under ultrasound conditions, thiazole compounds (6a) and (6b) were formed, respectively. Additionally, new derivatives (10) and (11) were synthesized through diazotizing compound (7), followed by coupling reactions with an activated methylene group (acetylacetone) and reactions with urea and thiourea, respectively, all under ultrasound conditions. All the synthesized compounds were characterized using spectroscopic techniques such as FT IR, 1H-NMR, and 13C-NMR spectra. The synthesized chemicals exhibited promising antimicrobial activities against human pathogenic bacteria strains (Escherichia coli and Staphylococcus aureus) and Candida albicans fungi, as assessed through the broth microdilution technique.

Abstract Background Antibiotic resistance genes will spread via soil fertilized with animal manure to food products. Especially plants whose harvested products can be consumed freshly are of concern. The aim of this study was to assess the impact of sulfadiazine (SDZ)-manured soil on the occurrence of sulfonamide (SA) resistance genes in freshly consumable plants. Methods Sulfadiazine-containing manure was administered via soil to lettuce and leek plants. At harvest, the rhizosphere soil, roots and leaves were investigated on the presence of SDZ-resistant bacteria and sul1 and sul2 genes via qPCR. Further, the impact of SDZ in manure on bacterial community and antibiotic resistance gene composition via amplicon sequencing and shotgun metagenomics was investigated in rhizosphere soils. Results Amendment of SDZ to manure resulted in an increase in sul2 genes in manure. However, abundances of sul genes in rhizosphere soils was strongly determined by plant growth and not by soil treatments with SDZ-manure, which was also the case for the bacterial community composition. Effects of SDZ at low or undetectable levels in leek rhizosphere soil became evident by bacterial association network and resistome analyses, and also in roots and leaves by SDZ-selective bacterial cultivation. Conclusions Antibiotic residues present in animal manure can lead to an increase in antibiotic resistances in food products. Plants play an important role in selection of antibiotic resistance genes present in manured soil. Transmission of antibiotic resistances via manure to the soil–plant ecosystem must be placed into the context of soils as vast reservoirs of ARGs.