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A photoelectrochemical (PEC) aptasensor us reported based on W6+-doped carbon nitride with carbon-rich structure (WCCN). WCCN exhibited excellent photoelectric conversion performance owing to the carbon-rich structure and W6+ doping. C atoms can replace the center N/edge N atoms to form a carbon-rich structure, improving the insufficient light absorption of CN in the visible region. Also, W6+ doping forms a directional electron transfer channel, achieving the efficient separation and transport of carriers. W6+ doping and carbon-rich structure can promote the generation, transfer, and separation of photogenerated carriers, further enhancing PEC performance. The fabricated PEC aptasensor based on WCCN demonstrated a wide detection range (3.92 ~ 588 pg L−1), a low detection limit (1.31 pg L−1, S/N = 3), good reproducibility, selectivity, stability, and practical application in actual water samples. This work explores the modification strategy of element doping for carbon nitride with high photoelectric property and offers a cost-effective and simplified method for the detection of pesticide residues. [ABSTRACT FROM AUTHOR]

Eighty milk samples, comprising raw cow's milk, pasteurised milk, ultra-high temperature milk, and camel milk, were collected randomly from supply centres from December 2022 to March 2023 in Gilan province, Iran. Aldrin, diazinon, and dichlorodiphenyltrichloroethane (DDT) were determined using high-performance liquid chromatography. Aldrin and diazinon were observed in all samples. Furthermore, 87.5% of the milk samples were contaminated with DDT. The raw milk sample showed the greatest concentration of aldrin, measuring 9.31 ± 0.80 µg L−1, and there was no significant difference with the camel milk. The samples of camel milk, raw milk, and ultra-high temperature milk demonstrated the greatest levels of DDT, whereas the lowest concentration was detected in pasteurised milk. In all samples, the maximum residue level (MRL) of Codex Alimentarius and the national Iran standard (20 µg L−1 for DDT) was only exceeded by 1.25% of the milk samples. [ABSTRACT FROM AUTHOR]

In accordance with Article 43 of Regulation (EC) No 396/2005, the European Commission has requested the European Food Safety Authority (EFSA) to organise a stakeholder consultation on the reasoned opinions for the following active substances, non‐approved for use as plant protection products in the European Union: azocyclotin, bifenthrin, chlorfenapyr, cyhexatin, diazinon, dicofol, endosulfan, fenarimol, fenpropathrin and profenofos. This technical report presents the outcome of the consultation, an appraisal of the data received and a conclusion on whether a reconsideration of the previous assessments will be needed based on the additional data collected. [ABSTRACT FROM AUTHOR]

[Display omitted] A single semiconductor-based photoelectrochemical (PEC) aptasensor usually faces a challenge of low sensitivity due to poor solar energy utilization and a high photogenerated carrier recombination rate. Herein, an ultra-thin carbon nitride nanosheet-coated In 2 O 3 (In 2 O 3 /CNS) S-type heterojunction-based PEC aptasensor has been established to achieve highly sensitive detection of diazinon (DZN) pesticide in water environment. Construction of S-type heterojunction induces a band shift and an electric field effect, enhancing light utilization and accelerating directional transmission of carriers, leading to outstanding PEC performance. The creation of internal electric field at interface ensures stable carrier transport. Additionally, ultrathin CNS structure can effectively shorten the transport path of carriers. The close coating of In 2 O 3 and CNS promotes the transfer of charge. The synergistic effects amplify the sensor's response, ultimately enabling the effective detection of DZN residue over a wide detection range (0.98 ∼ 980.0 pg mL−1), a low detection limit (0.33 pg mL−1, S/N = 3) and excellent accuracy in practical application (RSD < 5 %). This work provides a reference for the construction of a new S-type heterojunction-based PEC sensor. [ABSTRACT FROM AUTHOR]

In this study, a cheap, novel, ecofriendly and effective nanosorbent was synthesised with natural materials such as sand beach and eggshell for diazinon determination in natural water. The synthesised nanosorbent was successfully characterised using Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), field emission scanning- electron microscopy (SEM), vibrating sample magnetometer (VSM) and Brunauer–Emmett–Teller (BET) methods. Effective parameters were optimised for the extraction of diazinon and determination was done by UV-Vis spectroscopy at 248 nm. The method was linear in the range of 50–400 µg L−1 and the limit of detection was 6.9 µg L−1. Adsorption kinetic and isotherm studies were performed. Also, for measurement of diazinon in water samples of Gilan province, sampling was performed from important points such as river water, Anzali lagoon, well water, agricultural streams, and tap water. The results shows good spiked recovery (97.6–103.4%) in all samples. The accuracy of the method was also confirmed by the student's t -test with HPLC analysis of real samples. [ABSTRACT FROM AUTHOR]

Abstract MPs have raised significant public concern due to their role as carriers of organic contaminants in aqueous solutions. DZN is a non-systemic organophosphorus pesticide that poses risks to human and environmental health. This study aimed to investigate the adsorption of DZN onto PE MPs by examining factors such as PE dose, reaction time, pesticide concentration, and pH through experimental runs based on the Box‒Behnken model. According to the Langmuir model, the maximum adsorption capacity of PE for DZN was 0.35 mg/g. The results indicated that the highest adsorption rate of DZN (92%) was observed in distilled water, while the lowest adsorption rate (57%) was observed in municipal wastewater. The ΔH° and ΔS° values were obtained as − 0.16 kJ/mol and 54.41 J/(mol K), respectively. Therefore, regarding negative ΔG° values, it can be concluded that the adsorption of DZN onto PE MPs is an exothermic, highly disordered, and spontaneous process. The findings indicate a reduction in the adsorption rate of DZN as the concentrations of interfering compounds increase. These findings offer understanding of the interaction between MPs and organic contaminants, emphasizing the need for further studies and approaches to reduce their harmful impact on human health and the environment.

The present work discusses the removal of diazinon pesticide on the surface of magnetic graphene oxide composite via two different complementary methods specifically adsorption and Photo-Fenton degradation. Nanomagnetite (NG), graphene oxide (GO), and nanomagnetite/graphene oxide composite (NGO) were prepared as three solid materials. Developing TGA, nitrogen adsorption/desorption analysis, XRD, DRS, FTIR, pHpzc, and TEM, the morphological and physicochemical characteristics of the solid samples were examined. Characterization techniques proved that GO showed a higher specific surface area (505.5 m2/g) while NGO is characterized by a lower energy band gap (2.69 eV) and relatively high surface area (380.2 m2/g) in comparison with NG (2.90 eV and 103.5 m2/g). Both of GO and NGO are distinguished by the presence of different surface chemical functional groups. The main experimental application conditions were considered such as the effect of sample dose, pH, time, initial diazinon concentration, UV light power, and temperature. The results of the experiments showed that NGO adsorption capacity reached 149.54 mg/g at 25 °C orrelation coefficient values served as evidence that all generated solid samples follow nonlinear pseudo-second-order, Elovich, and Langmuir isotherm models. Using 1.5 g/L of catalyst mass and an initial diazinon concentration of 20 mg/L, the greatest percentage of diazinon Photo-Fenton degradation at 35 °C by NGO composite (99%) was reached after 50 min. Diazinon Photo-Fenton degradation is nonspontaneous, endothermic, fitting well the PFO kinetic model, Arrhenius models, and Eyring-Polanyi models. [ABSTRACT FROM AUTHOR]

This study's gaol is to ascertain the impact of diazinon about the condition of common carp, a significant fish species used for food in aquaculture (Cyprinus carpio). The LC50 of diazinon after 96 h was 9.5 mg/L in C. carpio (78.8 ± 5 g in weight). The fish were divided into six tanks as two treatments in order to ascertain the long-term effects of diazinon (three tanks per treatment). They were subjected to diazinon (2.37 mg/L; 25% LC50-96 h concentration) and 0 (control) for 4 days, 14 days, and 28 days before blood biochemical assays were performed on samples taken. Dry-chemistry analyzer was used to determination the Liver Function enzyme, also SOD and CAT was estimated by use spectrophotometer. At day four and day fourteen, the plasma SOD activity of the diazinonexposed fish did not significantly decrease in comparison to the control group; however, after day twenty-eight, the plasma SOD activity of the diazinon-exposed fish significantly increased in comparison to the control group. Diazinon exposure and control report a significant increase in serum CAT activity. Diazinon exposure increased significantly in serum ALT, AST and ALP activity compared to the control group. [ABSTRACT FROM AUTHOR]

Background: Ticks are the second most common vector of human infectious diseases after mosquitoes. Their transovarial transmission contributes to the maintenance of environmental diseases. This study evaluates the phytochemical screening and in vitro efficacy of Calpurnia aurea against the adult survival and egg hatchability of two transovarial transmission vectors: Amblyomma variegatum and Rhipicephalus microplus. Methods: Plant material was extracted using maceration techniques, and concentrated solutions of 12.5, 25, 50, 100, 200, and 400 ppm were prepared. Distilled water and diazinon were used as negative and positive controls, respectively. Ten adult ticks were exposed for 10 minutes, and dead ticks were counted after 24 hours of recovery. Twenty 15-day-old eggs were immersed for 10 minutes, and after 15 days of incubation, hatched and unhatched eggs were tallied. Preliminary phytochemical constituents were screened. A one-way analysis of variance and the probit regression model determined mean mortality and hatchability and estimated lethal and inhibitory concentrations, respectively. Results: The ethanolic and aqueous leaf extracts caused 10± 0.0% mortality in adult A. variegatum and R. microplus. The effective dose was LC50 of 27 and 29 ppm and LC50 of 37 and 41 ppm, respectively. At 400 ppm, the leaf ethanolic and aqueous extracts showed 18.7± 0.9% and 18.3± 1.7%; 18.3± 1.2% and 19.7± 0.3% egg hatching inhibition, respectively. The effective dose had an IC50 of 50 ppm and IC50s of 91 and 79 ppm, respectively. Flavonoids and saponins were found in both leaf and pod extracts. Conclusion: C. aurea extracts showed a more promising effect on tick survival and hatchability than synthetic diazinon. The susceptibility test indicated that the leaf extract could control vectors and contribute to environmental disease maintenance. Complex phytochemicals, especially phenolic compounds, are additional evidence of effectiveness in vector control. Further investigation of in vivo efficacy and advanced fractionation of phytochemicals is needed. [ABSTRACT FROM AUTHOR]

MPs have raised significant public concern due to their role as carriers of organic contaminants in aqueous solutions. DZN is a non-systemic organophosphorus pesticide that poses risks to human and environmental health. This study aimed to investigate the adsorption of DZN onto PE MPs by examining factors such as PE dose, reaction time, pesticide concentration, and pH through experimental runs based on the Box‒Behnken model. According to the Langmuir model, the maximum adsorption capacity of PE for DZN was 0.35 mg/g. The results indicated that the highest adsorption rate of DZN (92%) was observed in distilled water, while the lowest adsorption rate (57%) was observed in municipal wastewater. The ΔH° and ΔS° values were obtained as − 0.16 kJ/mol and 54.41 J/(mol K), respectively. Therefore, regarding negative ΔG° values, it can be concluded that the adsorption of DZN onto PE MPs is an exothermic, highly disordered, and spontaneous process. The findings indicate a reduction in the adsorption rate of DZN as the concentrations of interfering compounds increase. These findings offer understanding of the interaction between MPs and organic contaminants, emphasizing the need for further studies and approaches to reduce their harmful impact on human health and the environment. [ABSTRACT FROM AUTHOR]

The excessive and irrational use of organophosphate insecticides in our lives has resulted in a serious environmental problem, necessitating the proposal of novel and cost-effective plans to remove these organophosphate insecticides from agricultural or industrial wastewater. In this approach, we investigated the use of phyllosilicate clay as a low-cost and environmentally friendly adsorbent to eliminate an organophosphate insecticide (Diazinon DZN) from an aqueous medium. To achieve an adequate elimination of this insecticide from contaminated water, three main parameters including clay dose ( D c ) (0.1–1.5 g L−1), medium pH (5–9), and initial DZN concentrations ( C DZN ) (55–40 mg L−1) were optimized using a multivariable optimization based on Box-Behnken Design (BBD). The response surface method (RSM) and composite desirability function technique were used to find the ideal conditions for the three input variables and the adsorption amount ( Q e ) was selected as the output variable. The higher adsorption amount ( Q max ) was achieved with an adsorbent amount of 1.5 g L−1 in an acidic medium (pH = 5) at room temperature and a Diazinon initial dose of 25.85 mg L−1, with a maximum adsorbent loading of 12.20 mg g−1. The nonlinear modeling study showed that the adsorption kinetics of Diazinon follows the pseudo-second-order model. The thermodynamic study shows that the DZN removal process is exothermic, spontaneous, and of a stable configuration. [ABSTRACT FROM AUTHOR]

Background and purpose: Pesticides are well-known for their carcinogenic, mutagenic, and teratogenic properties, and they exhibit resistance to environmental degradation. Organophosphorus compounds represent one of the largest and most diverse groups of pesticides globally. Diazinon, an organophosphorus pesticide widely used in agriculture, was selected as the target pollutant for the present study. Materials and methods: The co-precipitation method was employed to synthesize zinc oxide nanocomposites coated on polyethylene terephthalate (PET). Subsequently, the nanoparticle structure was analyzed using XRD, FT-IR, SEM, and EDX analyses. The efficiency of diazinon sonocatalytic removal by zinc oxide nanocomposites coated on PET was investigated, and the impact of various parameters, including pH (3-11), nanocomposite dosage (0.2-2.5 g/L), initial diazinon concentration (5-50 mg/L), contact time (5-60 min), hydrogen peroxide concentration (2-50 mM), different gases (oxygen and nitrogen gas (2 L/min)), organic compounds (folic acid, citric acid, humic acid, EDTA, oxalate acid, phenol), radical scavengers (ammonium oxalate as h+ scavenger, benzoquinone as scavenger, tert-butyl alcohol as •OH scavengers), various processes (PET, US, PET/US, ZnO, ZnO-PET, ZnO/US, ZnO-PET/US), and recycled experiment, was evaluated. Firstly, the pH optimum was acquired to be 5, with changing pH and constant nanocatalyst dosage and initial diazinon concentration. The effects of different parameters on the removal of diazinon were investigated at the constant value of pH. Diazinon residual concentration was measured by a spectrophotometer (UV/VIS, DR5000) at a wavelength of 295 nm. Results: FT-IR and XRD analyses confirmed the coating of ZnO nanorods onto PET. Under optimal conditions, initial diazinon concentration of 20 mg/L, pH of 5, and nanocomposite dosage of 2.5 g/L for 60 minutes the sonocatalytic removal efficiency of diazinon reached 99.81%. The removal efficiency decreased from 100 to 40.15% as the diazinon concentration increased from 5 to 100 mg/L. The first-order rate constant (kobs) decreased from 0.123 to 0.0086 min-1, while R2 decreased from 0.985 to 0.9152, and electrical energy per order (EEo) increased from 181.073 to 2589.77 kWh.m-3 with increasing diazinon concentration. The sonocatalytic removal of diazinon increased with rising H2O2 concentration up to 5 mM. However, the addition of organic compounds and nitrogen gas led to a decrease in diazinon removal efficiency. The effectiveness of processes for pesticide removal from drinking water decreased due to anions scavenger activity. Examination of radical scavengers revealed that •OH radicals were the most active in diazinon removal. Notably, proper sonocatalytic activity in diazinon removal was observed even after six successive cycles. Intermediate products identified by GC-MS in the sonocatalytic removal process included diazoxon, IMP, hydroxy-diazinon, and diazinon-methyl-ketone. Conclusion: The findings suggest that zinc oxide coated on polyethylene terephthalate, as an affordable, practical, and environmentally friendly material, exhibits satisfactory efficiency for the sonocatalytic removal of diazinon from water environments.

Diazinon is an organophosphate pesticide commonly used by farmers. The use of diazinon can leave residues on agricultural products. Consumption of these products in the long term will cause health problems through oxidative stress mechanisms. Onion skin (Allium et al.) has a high content of flavonoids, which can neutralize oxidative stress. This study aims to determine the effectiveness of onion peel ethanol extract (OPEE) in reducing the plasma MDA level in diazinon-induced Wistar rats. Method This study is true experimental with a posttest-only control group design in vivo, using 28 samples divided based on a simple random sampling technique into four groups, i.e. the control group (K0), diazinon group (K1), OPEE groups P1 (300 mg/kgBW), P2 (600 mg/kgBW), P3 (900 mg/kgBW), P4 (1200 mg/kgBW), and P5 (2400 mg/kg BW). The examination of plasma MDA levels was carried out using the TBARS method. OPEE at doses of 300 mg/kgBW/day, 600 mg/kgBW/day, 900 mg/kgBW/day, 1200 mg/kgBW/day, and 2400 mg/kgBW/day significantly reduced the plasma MDA levels in diazinon-induced Wistar rats (p

The present research amid to investigate the toxic effect of diazinon (DZN) and assess the modulatory role of chitosan nanoparticle (ChNP), orange peel extract (OPE), spirulina platensis (SP) and curcumin nanoparticles (CNP) as feed additives in O. niloticus fish. A total of 900 fish were divided into six equal groups, each with 3 replicates by random distribution. The 1st group was kept as the control group which was fed a basal diet. The 2nd group (DZN) was given a basic diet and exposed to 1/10th of the 96-hour LC50 of DZN. The 3rd group (DZN+ChNP) was exposed to DZN (0.28 mg/L) + 1 gm ChNP/kg diet. The 4th group (DZN+OPE) was exposed to DZN (0.28 mg/L) + 2 gm OPE/kg diet. The 5th group (DZN+SP) was exposed to DZN (0.28 mg/L) + 5 gm SP/kg diet, while, the 6th group (DZN+SP) was exposed to DZN (0.28 mg/L) + 150 mg CNP/kg diet. Apart from feed conversion, DZN decreased fish's growth performance parameters as compared to the control, while these values were modulated with ChNP, SP or CNP supplement to fish with DZN exposure. Fish exposed to DZN had the lowest values Hb, RBCs WBCs, total protein, albumin and globulin and the highest values of ALT, AST and uric acid while dietary supplementation with ChNP, OPE, SP and CNP to DZN exposed fish restored their levels to the control values. Fish group fed diet supplemented with DZN+OPE or DZN+ChNP recorded the lowest value of ALT among all studied groups. DZN altered the lipid profile of exposed fish while the DZN+SP group had the best values of all lipid profile among all groups followed by DZN+CNP group. Fish exposed to DZN had lower serum lysozyme activity, immunoglobulin (M, A and G) levels and antioxidant parameters (SOD, GSH, CAT and TAC) while dietary supplementation of ChNP or OPE to DZN exposed fish had higher values for these traits but still under control values. The highest level of lipid peroxidation marker malondialdehyde (MDA) was observed in DZN group while dietary supplementation of ChNP or OPE to DZN exposed fish decreased the MDA level. According to the genetic distance and dendrogram for the analysis of genetic diversity between treatments, compared to control; it is clear that the highest genetic diversity was found with DZN group samples (4.80) while dietary treatments with ChNP, OPE or SP to DZN exposed fish showed the lowest diversity of (3.00, 3.32 and 3.87), respectively. It could be concluded that long-term exposure to a sub-lethal DZN dose resulted in growth retardation, haemato-biochemical alteration, immune depression, oxidative stress and genetic material damage of Nile tilapia. Furthermore, the antioxidant and protective properties of ChNP, OPE, SP, and CNP induced nearly total protection in fish exposed to DZN through diet.

Background and objectives: Diazinon (DZN) is a cholinesterase inhibitor widely used to relieve agricultural pests and upgrade the productivity of crops. Resveratrol (Res), as a phenolic plant compound, has a protective role against free radicals. This study intended to evaluate the impacts of Res on homeostatic disturbances induced by DZN in rats. Method: Twenty-four Wistar rats (4 weeks) were randomly distributed into four groups of six animals each. The first group (control group) received corn oil. The second group (Res group) received orally Res (20 mg/kg. The third group (DZN group) received the oral DZN (70 mg/kg); the fourth group (Res plus DZN group) was treated simultaneously with DZN (70 mg/kg) and Res (20 mg/kg); for a period of 5 weeks. The serum, liver, kidney, and heart levels of the Copper (Cu), zinc (Zn), iron (Fe), selenium (Se), and magnesium (Mg) as main trace elements are measured. Results: DZN treatment decreased significantly serum, liver, kidney, and heart levels of Cu, Zn, Fe, Se, and Mg in comparison with the control group. Res administration enhanced serum, liver, kidney, and content of heart elements compared to the DZN group. Conclusions: These results suggested that Res could ameliorate the homeostatic imbalance induced by DZN. Res had a protective effect against DZN-provoking heart, renal, and hepatic toxicity in animal models.

BackgroundPesticide exposure has been associated with adverse health effects. We evaluated relationships between proximity to agricultural insecticide applications and insecticides in household dust, accounting for land use and wind direction.MethodsWe measured concentrations (ng/g) of nine insecticides in carpet-dust samples collected from 598 California homes. Using a geographic information system (GIS), we integrated the California Pesticide Use Reporting (CPUR) database to estimate agricultural use within residential buffers with radii of 0.5 to 4 km. We calculated the density of use (kg/km2) during 30-, 60-, 180-, and 365-day periods prior to dust collection and evaluated relationships between three density metrics (CPUR unit-based, agricultural land area adjusted, and average daily wind direction adjusted) and dust concentrations. We modeled natural-log transformed concentrations using Tobit regression for carbaryl, chlorpyrifos, cypermethrin, diazinon, and permethrin. Odds of detection were modeled with logistic regression for azinphos-methyl, cyfluthrin, malathion, and phosmet. We adjusted for season, year, occupation, and home/garden uses.ResultsChlorpyrifos use within 1-4 km was associated with 1 to 2-times higher dust concentrations in both the 60- and 365-day periods. Carbaryl applications within 2-4 km of homes 60-days prior to dust collection were associated with 3 to 7-times higher concentrations and the 4 km trend was strongest using the wind-adjusted metric (p-trend = 0.04). For diazinon, there were 2-times higher concentrations for the 60-day metrics in the 2 km buffer and for the CPUR and wind-adjusted metrics within 4 km. Cyfluthrin, phosmet, and azinphos-methyl applications within 4 km in the prior 365-days were associated with 2-, 6-, and 3-fold higher odds of detection, respectively.ConclusionsAgricultural use of six of the nine insecticides within 4 km is an important determinant of indoor contamination. Our findings demonstrated that GIS-based metrics for quantifying potential exposure to fugitive emissions from agriculture should incorporate tailored distances and time periods and support wind-adjustment for some, but not all insecticides.

This study addresses water pollution challenges by employing photocatalysis as an effective solution. Titanium dioxide (TiO2) with unique characteristics is widely utilized in this approach. However, the design of nanosized TiO2 particles is crucial for enhancing photocatalytic performance during diazinon's photodegradation. As such, the TiO2 nanoparticles (NPs) were synthesized via the green sol‐gel method in this study, exhibit a mixed anatase‐brookite phase, a small particle size of 11.17 nm, and lower bandgap energy (3.00 eV) than pure anatase TiO2 of 3.20 eV, rendering them active under visible light. DFTB calculation was deployed to investigate the role of oxygen vacancies in reducing the bandgap energy. Experimentally measured (3.00 eV) and computationally (2.812 eV) determined bandgap energies align well. The TiO2 NPs demonstrate significant photocatalytic efficacy, degrading 73.3 % of diazinon within 210 min under sunlight, with a mineralization degree of 43.50 %, and 2‐isopropyl‐6‐methylpyrimidin‐4‐ol (IMP) was detected as the intermediate product. The photodegradation follows first‐order kinetics, and adsorption isotherm analysis fits the Langmuir model. ⋅O2− is identified as the predominant reactive oxygen species in the diazinon's photodegradation. Hence, the synthesized TiO2 NPs offer good reusability, maintaining a degradation efficiency of 67.4 % even after five cycles, showing good potential for wastewater treatment applications. [ABSTRACT FROM AUTHOR]

In accordance with Article 43 of Regulation (EC) 396/2005, EFSA received a request from the European Commission to propose fall‐back maximum residue levels (MRLs) for recently revoked Codex MRLs that have been previously implemented in the EU legislation. Overall, MRLs for 12 a.s. are concerned, i.e. chlormequat, diazinon, bifenthrin, fludioxonil, indoxacarb, difenoconazole, famoxadone, azoxystrobin, mandipropamid, emamectin benzoate, flutriafol and afidopyropen. In addition, EFSA was requested to evaluate the toxicological data assessed by JMPR related to pyrasulfotole, pyraziflumid, spiropidion and tetraniliprole. These are active substances have not been assessed previously at EU level. The assessment should allow to take a decision, if the CXLs adopted for these four a.s. can be implemented in the EU MRL legislation. [ABSTRACT FROM AUTHOR]

Background and purpose: Pesticides are well-known for their carcinogenic, mutagenic, and teratogenic properties, and they exhibit resistance to environmental degradation. Organophosphorus compounds represent one of the largest and most diverse groups of pesticides globally. Diazinon, an organophosphorus pesticide widely used in agriculture, was selected as the target pollutant for the present study. Materials and methods: The co-precipitation method was employed to synthesize zinc oxide nanocomposites coated on polyethylene terephthalate (PET). Subsequently, the nanoparticle structure was analyzed using XRD, FT-IR, SEM, and EDX analyses. The efficiency of diazinon sonocatalytic removal by zinc oxide nanocomposites coated on PET was investigated, and the impact of various parameters, including pH (3-11), nanocomposite dosage (0.2-2.5 g/L), initial diazinon concentration (5-50 mg/L), contact time (5-60 min), hydrogen peroxide concentration (2-50 mM), different gases (oxygen and nitrogen gas (2 L/min)), organic compounds (folic acid, citric acid, humic acid, EDTA, oxalate acid, phenol), radical scavengers (ammonium oxalate as h+ scavenger, benzoquinone as O2·- scavenger, tert-butyl alcohol as •OH scavengers), various processes (PET, US, PET/US, ZnO, ZnO-PET, ZnO/US, ZnO-PET/US), and recycled experiment, was evaluated. Firstly, the pHoptimum was acquired to be 5, with changing pH and constant nanocatalyst dosage and initial diazinon concentration. The effects of different parameters on the removal of diazinon were investigated at the constant value of pH. Diazinon residual concentration was measured by a spectrophotometer (UV/VIS, DR5000) at a wavelength of 295 nm. Results: FT-IR and XRD analyses confirmed the coating of ZnO nanorods onto PET. Under optimal conditions, initial diazinon concentration of 20 mg/L, pH of 5, and nanocomposite dosage of 2.5 g/L for 60 minutes the sonocatalytic removal efficiency of diazinon reached 99.81%. The removal efficiency decreased from 100 to 40.15% as the diazinon concentration increased from 5 to 100 mg/L. The first-order rate constant (kobs) decreased from 0.123 to 0.0086 min-1, while R² decreased from 0.985 to 0.9152, and electrical energy per order (EEo) increased from 181.073 to 2589.77 kWh.m-3 with increasing diazinon concentration. The sonocatalytic removal of diazinon increased with rising H2O2 concentration up to 5 mM. However, the addition of organic compounds and nitrogen gas led to a decrease in diazinon removal efficiency. The effectiveness of processes for pesticide removal from drinking water decreased due to anions scavenger activity. Examination of radical scavengers revealed that •OH radicals were the most active in diazinon removal. Notably, proper sonocatalytic activity in diazinon removal was observed even after six successive cycles. Intermediate products identified by GC-MS in the sonocatalytic removal process included diazoxon, IMP, hydroxy-diazinon, and diazinon-methyl-ketone. Conclusion: The findings suggest that zinc oxide coated on polyethylene terephthalate, as an affordable, practical, and environmentally friendly material, exhibits satisfactory efficiency for the sonocatalytic removal of diazinon from water environments. [ABSTRACT FROM AUTHOR]

The kinetics of diazinon degradation in soils as affected by the presence of potentially toxic elements was studied. Metal (Zn2+, Cd2+, V3+ and Mn2+) treated soils as well as the control soils were spiked with diazinon at two concentrations of 10, and 50 mg kg-1. The residual diazinon concentrations were measured by corona discharge-ion mobility spectrometry at 0, 1, 10, 30, and 60 d. Degradation time (DT50) was calculated using three kinetic models. At 10 and 50 mg kg-1 of diazinon, no residual concentration could be detected at the day 30 and 60, respectively. In the Shervedan soil, the DT50 values for 10 and 50 mg kg-1 spiked diazinon concentration ranged from 0.51 to 2.3 d and 2.87 to 5.31 d, respectively. The greatest and the lowest DT50 values were consistently obtained in the control and V-treated soil. In the Lavark and Chamaseman soil, the pattern was similar to that of the Shervedan soil, except that Zn was more stimulatory than V in the Lavark soil. In general, metal-treated soils revealed lower diazinon concentrations. For the first time, it is reported that V can enhance the rate of diazinon degradation in soils. Overall, it is concluded that V and Zn are the most stimulatory potentially toxic elements for enhancing diazinon degradation in the soils. Therefore diazinon degradation time in the metal polluted soils is generally shorter. [ABSTRACT FROM AUTHOR]

Controlling the structure of cerium dioxide (CeO2)-based photocatalysts for the removal of organic contaminants in water is essential. Herein, GO/Fe3O4/CeO2 heterojunction photocatalyst is designed by a clear and simple method for photodegradation of diazinon under visible-light excitation. SEM, EDS, XRD, FTIR, VSM, and UV–vis were used to analyze the crystallinity and morphology of the GO/Fe3O4/CeO2 heterojunction. The UV–Vis analysis revealed a bandgap value of 3.19, 3.08, and 2.98 eV, respectively, for GO, GO@Fe3O4, and GO@Fe3O4@CeO2. The effects of important parameters such as pH (2.0–9.0), photocatalyst dose (10–40 mg), and contact time (0–180 min) were also investigated. The maximum diazinon degradation rate was found to be 97.9% in 60 min. In conclusion, the results indicated that GO@Fe3O4@CeO2 nanocomposite could be used as an efficient photocatalyst for the degradation of organic contaminants from water medium. [ABSTRACT FROM AUTHOR]

Increasing water consumption and its pollutants threatens primary water supply sources due to the growth of various industries and production of wastewater including agriculture. Scientists attempt to remove water pollution using recyclable materials, especially composites and recyclable polymer nanocomposites. Diazinon is a phosphorus pesticide being widely used as a pesticide in agriculture, and its residues are found in aquatic ecosystems. In this study, the efficiency of nanocomposites prepared from rice husk to remove diazinon from water was investigated. Residual diazinon concentrations were determined by high performance liquid chromatography (HPLC) instrument. The nanocomposite properties were characterized using FESEM, FTIR, XRD, DLS, zeta potential, CHN and EDX techniques. The parameters including pH, contact time, adsorbent dose, and diazinon concentration were investigated on the removal rate by nanocomposites. Isotherm models were used to study adsorption capacity of the nanocomposite. FTIR and FESEM analyses showed uniform distribution of particles in the polymer composite. The average particle size of nanocomposite was 63.57 ± 13.47 nm, and C appeared to be the most abundant atom (53.35%) in particles. The best removal conditions included pH=7 and the crossing time of 20 minutes. The removal efficacy was highest at 20 ppm of diazinon and 0.1 g of nanocomposite. The adsorption process of the nanocomposite was more consistent with the Langmuir isotherm (R2>0.98), which signifies the homogeneous adsorption of the adsorbent. The results of this study revealed that nanocomposites prepared from rice husk can be considered as a suitable adsorbent to remove diazinon from aqueous media. [ABSTRACT FROM AUTHOR]

A quantitative method based on quick, easy, cheap, effective, rugged, and safe technique (QuEChERS) sample extraction and ultra-performance liquid chromatography/tandem mass spectrometry (UHPLC-MS/MS) was evolved for the determination of 47 pesticide residues in fresh Mazafati date fruits from Bam City of Kerman Province, Iran. The recoveries for selected pesticides ranged from 88 to 110% with a relative standard deviation (RSD) of less than 20% at concentrations of 0.05 and 0.1 mg kg−1. The proposed method had a linear range from the limit of quantification (LOQ) to 1.00 mg kg−1, and the LOQ of the 47 pesticides was ≤ 0.005 mg kg−1. The coefficients of determination (R2) were more than 0.99. This technique was used on 12 fresh date fruits samples, three water samples, and three soil samples with three replications per sample. Forty-seven pesticide were detected collectively, but only diazinon was detected in the date fruit samples. The mean value of diazinon residues was 0.037 mg kg−1, and the concentration of diazinon in most samples was below the national maximum residue limit (MRL) for date fruit (0.05 mg kg−1). Among the pesticides measured, diazinon residues were also detected in the water samples, but not in the soil samples. The dietary intake assessment showed no health risk to humans from the consumption of fresh date fruit concerning the pesticides investigated. [ABSTRACT FROM AUTHOR]

Background: Modern strategies to alleviate the harmful effects of organophosphate pesticide diazinon (DN) abnormalities were focused mainly on using natural compounds or their derivatives. DN is an organophosphate compound that causes many health abnormalities in humans due to its usage as an insecticide in agriculture. TQ is one of the beneficiary active principles derived from plant sources that has pharmacological benefits. Aim: This research reveals the therapeutic potential of thymoquinone (TQ) on DN-induced myocardial infarction (MI) in rats. Materials and Methods: Male Sprague–Dawley rats were procured, acclimatized, and divided into four groups of six animals each with feed and water ad libitum. MI was induced in rats with a dose of 25 mg/kg DN by oral gavage and TQ in a dose of 20 mg/kg p.o. for the treatment. After animal sacrifice at the end of the experimental period, serum and heart tissue samples were collected and processed appropriately for various analyses such as changes in the body weight, heart weight, marker enzymes, oxidative markers, non-enzymatic and enzymatic antioxidants, inflammatory cytokines, histopathological studies, and cardiac-specific markers. Results: DN-induced toxicity depicted decreased body weight (167.83 ± 4.62), heart weight (0.9 ± 0.06), and heart-to-body weight ratio (0.54 ± 0.03). Also, elevated marker enzymes (147.33 ± 20.85, 407.5 ± 31.3, and 110.67 ± 9.65 for CK-MB, AST, and ALT, respectively), elevated oxidative markers (12.87 ± 1.34, 125.17 ± 9.95, and 80.17 ± 5.78 for serum MDA, heart MDA, and heart GSSG, respectively), decreased enzymatic- and non-enzymatic antioxidants (3.15 ± 0.42, 12.23 ± 1.02, 5.75 ± 0.46, 2.02 ± 0.26, 0.72 ± 0.07, 18.05 ± 1.04, 8.62 ± 0.65, and 45.8 ± 2.43 for SOD, CAT, GST, GPx, heart GSH, serum GSH, vit.E, and vit.C, respectively), damaged cellular architecture, elevated inflammatory cytokines, and cardiac-specific markers were noticed. Discussion: TQ significantly reduced the toxicities produced by DN in almost all the above parameters. The beneficial effect of DN could be attributed to the influential effect of DN on cardiac-specific Nrf2/HO1-related pathways. Conclusion: These results suggest that TQ exerts protection against MI and could serve as a promising candidate for drug development. [ABSTRACT FROM AUTHOR]

In this study, the extraction of rare earth elements (REEs) from chloride solutions after leaching REE carbonate concentrate with solutions of the mixtures of P507 (2-ethylhexylphosphonic acid mono-2-ethylhexyl ester) and Cyanex 272 (bis(2,4,4-trimethylpentyl)phosphinic acid) (1:1) at various concentrations was experimentally studied. It was shown that the distribution ratios of all REEs decrease with the increasing concentration of these metals in the initial solution, which is associated with the loading of the organic phase. The most significant improvement in the extraction is observed for the heavy group of rare earth elements. The extractability of REEs increases with the increasing atomic number of the element, as is typical for the extraction of these metals with acidic organophosphorus extractants. The data obtained show that the separation factors of adjacent rare earth elements decrease slightly with the increasing concentration of metals in the initial aqueous solution. Increasing the concentration of the extractant mixture does not have a significant effect on the values of the adjacent REE separation factors. The data obtained on the distribution ratios and separation factors made it possible to propose a flow sheet for the separation of rare earth elements with the production of Y, Ho, Tb and Dy. [ABSTRACT FROM AUTHOR]

Diazinon, an organophosphorus insecticide, is predominantly removed through photodegradation and biodegradation in the environment. However, photodegradation can generate diazoxon, a highly toxic oxidation byproduct, while biodegradation is hard to complete mineralize diazinon, showing limitations in both methods. In this study, we provided an efficient strategy for the complete and harmless removal of diazinon by synergistically employing biodegradation and photodegradation. The diazinon-degrading strain X1 was capable of completely degrading 200 μM of diazinon into 2-isopropyl-6-methyl-4-pyrimidinol (IMP) within 6 h without producing the highly toxic diazoxon. IMP was the only intermediate metabolite in biodegradation process, which cannot be further degraded by strain X1. Through RT-qPCR and prokaryotic expression analyses, the hydrolase OpdB was pinpointed as the key enzyme for diazinon degradation in strain X1. Photodegradation was further used to degrade IMP and a pyridazine ring-opening product of IMP was identified via high resolution mass spectrometry. The acute toxicity of this product to aquatic organisms were 123 times and 6630 times lower than that of diazinon and IMP, respectively. The stepwise application of biodegradation and photodegradation was proved to be a successful approach for the remediation of diazinon and its metabolite IMP. This integrated method ensures the harmless and complete elimination of diazinon and IMP within only 6 h. The research provides a theoretical basis for the efficient and harmless remediation of organophosphorus insecticide residuals in the environment.

The high toxicity and bio-stability of organochlorine pesticides have made organophosphorus pesticides (OPPs) more preferred today. Diazinon is one of the most widely used insecticides in the group of OPPs, which has high stability in the environment and causes neurobehavioral side effects in case of long-term exposure to humans. The present study aims to fabricate the PbO2 electrocatalyst on a graphite sheet (G/PbO2) and use it as a non-active anode for diazinon degradation. The effect of independent variables such as solution pH, current applied to the electrodes, initial concentration of diazinon and reaction time on the removal efficiency of the pesticide was studied. SEM and XRD results showed that lead dioxide crystals in the β-PbO2 phase were formed as compact pyramidal clusters on the surface of the anode. At solution pH 8, diazinon removal efficiency was significantly improved. However, in mild operating conditions (solution pH = 5 and a current = 0.4 A), diazinon removal efficiency with initial concentrations of 20 and 100 mg/L after 90 min of reaction was 100% and 70%, respectively. After optimizing the independent variables effective in the diazinon removal, the mineralization pathway was proposed considering intermediates identified by LC-MS analysis. The results of the present study confirm that anodic oxidation with PbO2 electrocatalyst can be an effective method for the degradation and mineralization of diazinon pesticide.

Introduction: Contamination of water sources with toxins is an environmental problem and a serious threat to the health of societies. This study aimed to ascertain the remaining levels of toxins in urban drinking water networks and compute the water quality index. Materials and Methods: To examine the residual concentration of diazinon, chlorpyrifos, and dichlorvos in urban drinking water distribution networks, 35 underground and surface water sources were sampled in Tiran-o-Karvan in Isfahan province, Iran. GC-ECD device was used to analyze the samples. Results: Diazinon was not observed in any of the sampling seasons. The maximum concentration of chlorpyrifos and dichlorvos was 61 and 100 ppb, respectively. Although chlorpyrifos was seen more in the hot season and dichlorvos in the cold season, the mean concentration of these toxins in different seasons was lower than the guidelines of Iran and the World Health Organization (WHO). The mean concentration of nitrate, and hardness, in wet and dry seasons was 46.23 and 46.42, and 343.7 and 338.8 mg/l, respectively. Conclusion: The mean and standard deviation of quality index of Iran's water resources (IRWQI) in wet and dry seasons were 52.16 ± 45.3 and 50.69 ± 15.8, respectively. The residual concentration of toxins in some water sources of this city exceeded the guidelines of Iran and the WHO in summer and spring.

The study aimed to analyze how variations in TiO2/NaOH mole ratio, stirring time, and washing pH affect the formation process of TiO2 nanotubes (TNT) through one-stage hydrothermal. TiO2 micro powder was mixed with 10M NaOH with the variation of TiO2/NaOH mole ratio (0.005:1, 0.015:1, and 0.025:1). The hydrothermal process was then conducted at 130 ℃ in an autoclave for 24 h with stirring time intervals of 10, 15, and 20 minutes/h. The samples underwent 1 M HCl washing to produce diverse pH variations (pH = 2, pH = 3, and pH = 4). Characterization of the synthesized TNT was conducted using SEM, TEM, XRD, SAA, and UV-Vis DRS. After analysis of the micrographs revealed the fiber shape of the particles, it was noted that TNT particle size increased due to smaller mole ratio variation, longer stirring, and lower pH. The synthesized TNT featured a tubular morphology with an inner diameter of 3.30 nm, an outer diameter of 6.15 nm, and a wall thickness of 1.64 nm. The increase in sodium titanate content of the sample results in an increase in surface area. Additionally, small pore size contributes towards an increase in both surface area and total pore size. The best result of the TNT photocatalytic test against diazinon can be observed in the fifth sample with a mole ratio of 0.025:1, stirring time of 20 minutes/h, and washing pH of 3. With an irradiation time of 210 min, diazinon degradation reached 90%. Copyright © 2023 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Organophosphorous (OP) pesticides can cause many human diseases. In this study, the separation and determination of two organophosphorous pesticides (diazinon and methyl-parathion) in biological samples using solid-phase extraction method prior to their measurements by high‐performance liquid chromatography (HPLC) were investigated. Herein, a new functionalized cerium-based metal–organic framework (MOF) bearing oxime moiety, denoted here UiO-66(Ce)-MO, was synthesized through two-synthetic steps from the pristine UiO-66(Ce) and then applied as an efficient porous adsorbent for the extraction of pesticides from biological samples. Various techniques including Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Brunauer–Emmett–Teller (BET) analysis were used for the description of adsorbent. The optimization of variables was performed by Box–Behnken design combined with response surface methodology. The factors' effects including pH, eluent volume (EV), sample flow rate (SF) and eluent flow rate (EF) were also examined. The optimum conditions for both compounds were pH 5.5, eluent volume 0.6 mL, SF 2 mL min−1, and EF 0.2 mL min−1, leading to 97.1% and 96.0% removal of diazinon and methyl-parathion, respectively. Under the optimum conditions, the maximum adsorption capacity was obtained 454.5 mg g−1 for methyl-parathion and 476.2 mg g−1 for diazinon. The limit of detection (LOD) was found to be 0.04 μgL−1 for diazinon and 0.06 μgL−1 for methyl-parathion. Sensitivity analysis showed that pH plays a significant role on the efficiency of both organic pollutants. Remarkably, the results showed that this adsorbent outperforms the other UiO-66(Ce) samples and is suitable for separation and determination of these organic materials from water and biological real samples (blood plasma and urine). A porous oxime-functionalized Ce-MOF, UiO-66(Ce)-MO, was synthesized and applied for efficient extraction and determination of trace amounts of methyl-parathion and diazinon from water and biological samples. [ABSTRACT FROM AUTHOR]

The WO3-Fe3O4/reduced graphene oxide (rGO) composite was synthesized with a hydrothermal method for the photocatalytic removal of diazinon (DZ) in visible light. The influence of catalyst concentration (0.5–1.5 g L−1), pH (5–9), and initial pollutant value (5–15 mg L−1) on the pesticide degradation was studied. The performance of the WO3-Fe3O4/rGO nanocomposite for DZ degradation under visible light shows 94% degradation of 5 mg L−1 DZ for 100 min with 1 g L−1 nanocomposite, and the degradation kinetic was modeled in pseudo-first order (PFO) and the maximum kobs was 0.0248 min−1. The photocatalytic mechanism and the intermediates of DZ degradation were identified. In addition, the WO3-Fe3O4/rGO catalyst showed reusability after 4 runs. The results of this work illustrate that the WO3-Fe3O4/rGO nanocomposite can be applied for real use owing to its high catalytic performance. [ABSTRACT FROM AUTHOR]

Background: Multiple pesticides are often used in combination for plant protection and public health. Therefore, it is important to analyze the physiological changes induced by multiple pesticides exposure. The objective of this study was to investigate the combined toxicity of the widely-used organophosphorus and pyrethroid pesticides diazinon, dimethoate, and cypermethrin. Methods: Male Wistar rats were administrated by gavage once daily with the three pesticides individual or in combination for consecutive 28 days. The metabolic components of serum and urine samples were detected by using 1H nuclear magnetic resonance (NMR)-based metabolomics method. Histopathological examination of liver and kidneys and serum biochemical determination were also carried out. Results: The results showed that after the 28-day subacute exposure, serum glutamic transaminase and albumin were significantly increased and blood urea nitrogen was significantly decreased in the rats exposed to the mixture of the pesticides compared with the control rats, suggesting that the co-exposure impaired liver and kidney function. Metabolomics analysis indicated that the indicators 14 metabolites were statistically significant altered in the rats after the exposure of the pesticides. The increase in 3-hydroxybutyric acid in urine or decrease of lactate and N-acetyl-L-cysteine in serum could be a potentially sensitive biomarker of the subchronic combined effects of the three insecticides. The reduction level of 2-oxoglutarate and creatinine in urine may be indicative of dysfunction of liver and kidneys. Conclusion: In summary, the exposure of rats to pesticides diazinon, dimethoate, and cypermethrin could cause disorder of lipid and amino acid metabolism, induction of oxidative stress, and dysfunction of liver and kidneys, which contributes to the understanding of combined toxic effects of the pesticides revealed by using the metabolomics analysis of the urine and serum profiles. [ABSTRACT FROM AUTHOR]

Pesticides are on the list of substances that are routinely monitored by agencies and organizations in various natural environments and habitats. Diazinon (DZN) is the active ingredient in more than 20 agricultural pesticides, it causes the most damage and has been prohibited in many countries around the world. The final product CoWO4/g-C3N4 Z-scheme heterojunction was successfully synthesized in this work, where CoWO4 nanoparticles were deposited on the surface of g-C3N4. CoWO4/g-C3N4 structure allowed for the efficient separation of photo-generated electron-hole pairs, with electrons at the CoWO4 CB migrating to the g-C3N4 VB and preserving the electrons at the g-C3N4 CB and holes in the CoWO4 VB. The photodegradation efficiency of DZN using CoWO4/g-C3N4 Z-scheme heterojunction was investigated, as compared with its precursors, such as CoWO4, and g-C3N4. CoWO4/g-C3N4 Z-scheme heterojunction demonstrated the highest degradation capacity for DZN removal. Based on the results, the photocatalysis of the CoWO4/g-C3N4 Z-scheme heterojunction can be recycled for the effective removal of DZN by simple washing after three runs, proving the heterojunction's stability and suggesting CoWO4 as a promising material for the removal of DZN from contaminated water sources. [ABSTRACT FROM AUTHOR]

Pesticides are on the list of substances that are routinely monitored by agencies and organizations in various natural environments and habitats. Diazinon (DZN) is the active ingredient in more than 20 agricultural pesticides, it causes the most damage and has been prohibited in many countries around the world. The final product CoWO4/g-C3N4 Z-scheme heterojunction was successfully synthesized in this work, where CoWO4 nanoparticles were deposited on the surface of g-C3N4. CoWO4/g-C3N4 structure allowed for the efficient separation of photo-generated electron-hole pairs, with electrons at the CoWO4 CB migrating to the g-C3N4 VB and preserving the electrons at the g-C3N4 CB and holes in the CoWO4 VB. The photodegradation efficiency of DZN using CoWO4/g-C3N4 Z-scheme heterojunction was investigated, as compared with its precursors, such as CoWO4, and g-C3N4. CoWO4/g-C3N4 Z-scheme heterojunction demonstrated the highest degradation capacity for DZN removal. Based on the results, the photocatalysis of the CoWO4/g-C3N4 Z-scheme heterojunction can be recycled for the effective removal of DZN by simple washing after three runs, proving the heterojunction's stability and suggesting CoWO4 as a promising material for the removal of DZN from contaminated water sources. [ABSTRACT FROM AUTHOR]

Diazinon has been popular neurotoxic organophosphate cholinesterase-inhibiting pesticide for decades because it reliably kills a broad spectrum of arthropods associated with human health hazards and agricultural economic losses. Diazinon does not only affect arthropods, however; it is also one of the most common long-lasting environmental contaminants of air, soil, and water, creating direct and indirect toxic threats to vertebrate populations including birds, fish, mammals, and humans. To minimize and eventually eliminate exposure of Iran's wildlife and human populations to diazinon, the Iran Plant Protection Organization banned the import of technical-grade diazinon on 23 September 2019, and regulated phasing out all domestic use by 23 September 2022. This regulation will lead to significant decrease in use of diazinon in Iran, facilitating wildlife-friendly farming, reducing threats to Iran's bird, fish, and wildlife populations, improving the quality of life for Iran's human population, and perhaps inspiring other countries in the region to also ban diazinon. [ABSTRACT FROM AUTHOR]

A two-step method comprising hydrothermal processing and photodeposition was used to synthesize core–shell nanocomposites of silver-coated silicon dioxide and titanium dioxide (Ag-SiO2@TiO2). The shape, identification of crystalline components, and substance of Ag-coated SiO2@TiO2 nanocomposites were examined using SEM, X-ray diffraction, and Fourier-transform infrared spectra. This research used a photocatalytic batch system to degrade diazinon from an aqueous solution using Ag nanoparticles photo-deposited on a SiO2@TiO2 core–shell structure at a mass concentration of 6%. The effect of five operating factors on pollutant oxidation (RSM) was studied using the central composite design (CCD) of response surface methodologies. Under optimal conditions of catalyst concentration (30 mg/L), diazinon concentration (10 mg/L), pH = 7, H2O2 (200 mg/L), and reaction time of 90 min, the Ag nanoparticle was shown to be very effective at treating diazinon-contaminated water, with a maximum removal efficiency of 99.74%. The anticipated R2 matched the modified R2 very well, indicating that the predictions and the experiments were in great agreement. The predictions made by the CCD modeling were correct, as evidenced by the lab data. [ABSTRACT FROM AUTHOR]

Graphene oxide/polydopamine-polyacrylamide nanocomposite as sorbent for dispersive micro-solid phase extraction of diazinon from environmental and food samples was synthesised and coupled with high-performance liquid chromatography-ultraviolet detector. The prepared sorbent was characterised by analytical techniques such as Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy–energy-dispersive spectroscopy and thermal gravimetric analysis. Main parameters affecting extraction efficiency of diazinon using dispersive micro-solid phase extraction such as sorbent amount, elution solvent and its volume, sorption and desorption times and pH of sample solution were investigated and optimised. The optimum values are as follow; sorbent amount, 0.2 g; elution solvent, methanol; elution solvent volume, 2.5 mL; sorption time, 10 min; desorption time, 4 min and pH of sample solution, 3. Under the optimised conditions, method detection limit and limit of quantitation values were 0.24 and 1.0 ng/mL, respectively. Relative recovery data for several real samples were obtained within the range of 82.0–98.0% with a relative standard deviation less than 6.5%. The proposed method was successfully applied to quantitative determination of diazinon in several environmental and food samples. [ABSTRACT FROM AUTHOR]

The aim of this study is to determine the effects of 50% of 96 h LC50 (5.25 ppm) diazinon on the expression of superoxide dismutase (SOD) enzyme genes (sod1, sod2, and sod3b) and SOD enzyme activity at the end of 24, 48, 72, and 96 h in platyfish liver and gill tissues. To this end, we determined the tissue-specific distribution of sod1, sod2, and sod3b genes and performed in silico analyses in platyfish (Xiphophorus maculatus). It was determined that malondialdehyde (MDA) level and SOD enzyme activity were increased in the liver [(43.90 EU mg protein−1 (control), 62.45 EU mg protein−1 (24 h), 73.17 EU mg protein−1 (48 h), 82.18 EU mg protein−1 (72 h), 92.93 EU mg protein−1 (96 h)] and gill [(16.44 EU mg protein−1 (control), 33.47 EU mg protein−1 (24 h), 50.38 EU mg protein−1 (48 h), 64.62 EU mg protein−1 (72 h), 74.04 EU mg protein−1 (96 h)] tissues of platyfish exposed to diazinon, while the expression of the sod genes was down-regulated. The tissue-specific distribution of the sod genes varied, with the tissues and the sod genes expression were being predominant in the liver (628.32 in sod1, 637.59 in sod2, 888.5 in sod3b). Thus, the liver was considered a suitable tissue for further gene expression studies. Based on the phylogenetic analyses, platyfish sod genes can be reported to be orthologs of sod/SOD genes from other vertebrates. Identity/similarity analyses supported this determination. Conserved gene synteny proved that there are conserved sod genes in platyfish, zebrafish, and humans. [ABSTRACT FROM AUTHOR]

The most prevalent component of the volatile oil found in Nigella sativa seeds is thymoquinone (TQ). As well as being used as food supplements, the seeds and oil are also utilized in traditional medicine to treat a variety of ailments. The purpose of this investigation was to determine whether TQ could protect rats from acute nephrotoxicity caused by diazinon (DZN). Six equal groups of thirty six adult male Wistar rats were created at random. Group 1 (G1) was maintained in typical control circumstances and given saline daily intragastric (IG) for 4 weeks; G2 was administered 0.1 mL olive oil IG for 4 weeks; G3 was administered 0.1 mL DMSO IG for 4 weeks; G4 was administered IG TQ at a dose of 10 mg/kg B.W. daily for 4 weeks; G5 was administered IG DZN at a dose of 15 mg/kg B.W. daily for 4 weeks; G6 was administered TQ intragastric (IG) daily, one hour before DZN at the same dose as in G4 and G5, for 4 weeks. The findings showed that TQ reduces the renal dysfunctions brought on by DZN by restoring urea and creatinine levels as well as oxidative indicators. Although the expression of Kelch-like ECH-associated protein 1 (Keap1) was also elevated, overexpression of nuclear factor erythroid 2-related factor 2 (Nrf2) also enhanced the expression of heme oxygenase-1 (HO-1), and Nuclear factor kappa B (NFκB) in renal tissue. Also, TQ increased antiapoptotic (BCL2) factors and decrease proapoptotic (BAX) factors. In conclusion, TQ is helpful in the prevention and management of acute nephrotoxicity brought on by DZN. [ABSTRACT FROM AUTHOR]

The present study analyzes the efficacy of N-acetyl cysteine (NAC) against diazinon (DZN)-induced nephrotoxicity in male Wistar rats. Rats were divided into five groups with six animals in each group: Group 1 (G1) was maintained in typical control circumstances and given saline once daily intragastric (IG) for 4 weeks; G2 was administered 0.1 mL olive oil IG for 4 weeks; G3 was administered IG NAC 150 mg/kg daily as an aqueous solution for 4 weeks; G4 was administered IG diazinon at a dose of 15 mg/kg daily for 4 weeks; and G5 was administered IG NAC daily one hour before diazinon at the same dose in G3 and G4 for 4 weeks. Sub-chronic exposure to DZN impairs the kidney structure and function, as evidenced by the histopathology, immunohistochemistry, and gene expression of NLRP3, NFκB, IKB, BCL2, BAX mRNA. Our findings showed that NAC reduces the renal dysfunctions induced by DZN by restoring urea and creatinine levels as well as oxidative indicators. Moreover, serum inflammatory markers (IL-1β and TNF-α) concentrations were ameliorated by NAC treatment. However, NAC has shown to play a beneficial role against nephrotoxicity by reversing the cytoarchitecture and downregulation of inflammatory (NLRP3, NFκB, IKB) and apoptotic (BAX) as well as upregulated BCL2 genes and proteins in kidney tissues, bringing them to near-normal levels. Moreover, IHC examination of renal tissue revealed the attenuation of expression of TNF-α. Therefore, NAC could be potentially used to protect the kidneys from pathological changes induced by DZN. [ABSTRACT FROM AUTHOR]

Diazinon (DNZ) is one of the most widely used organophosphorus poisons, which plays an important role in chemical pest control by controlling a wide range of chewing and sucking pests in gardens and fields. Diazinon causes death in living organisms by reducing cholinesterase and disrupting nerve cells. In this research, the effect of Rosa damascena extract against DNZ toxicity and oxidative damage induced by DZN in mice was studied. The mice toxified with DNZ (32.5 mg kg-1, intraperitoneally) and treated by pralidoxime (PM) (20 mg kg-1, intraperitoneally) or R. Damascena extract (50, 100, 200 mg kg-1, orally) daily for two weeks. In the end, the acetylcholinesterase (AchE), ferric-reducing antioxidant power (FRAP), Malondialdehyde (MDA), ALT, AST, ALP, and total bilirubin were assayed. DZN administration significantly lowered the AchE, and FRAP and increased the MDA (P < 0.05). However, R. Damascena extracts treatment caused a significant reduction in MDA level and restored the levels of AchE and FRAP as well as significantly prevented the DZN-induced increase in liver aminotransferases, ALP, and total bilirubin. We found that R. Damascena administration nearly eliminated DZN-induced toxicity by preventing oxidative stress in mice. [ABSTRACT FROM AUTHOR]

The study aimed to analyze how variations in TiO2/NaOH mole ratio, stirring time, and washing pH affect the formation process of TiO2 nanotubes (TNT) through one-stage hydrothermal. TiO2 micro powder was mixed with 10M NaOH with the variation of TiO2/NaOH mole ratio (0.005:1, 0.015:1, and 0.025:1). The hydrothermal process was then conducted at 130 °C in an autoclave for 24 h with stirring time intervals of 10, 15, and 20 minutes/h. The samples underwent 1 M HCl washing to produce diverse pH variations (pH = 2, pH = 3, and pH = 4). Characterization of the synthesized TNT was conducted using Scanning Electron Microscope (SEM), Transmission Electron Microscope (TEM), X-ray Diffraction (XRD), Surface Area Analyzer (SAA), and Ultra Violet Visible Diffuse Reflectance Spectroscopy (UV-Vis DRS). After analysis of the micrographs revealed the fiber shape of the particles, it was noted that TNT particle size increased due to smaller mole ratio variation, longer stirring, and lower pH. The synthesized TNT featured a tubular morphology with an inner diameter of 3.30 nm, an outer diameter of 6.15 nm, and a wall thickness of 1.64 nm. The increase in sodium titanate content of the sample results in an increase in surface area. Additionally, small pore size contributes towards an increase in both surface area and total pore size. The best result of the TNT photocatalytic test against diazinon can be observed in the fifth sample with a mole ratio of 0.025:1, stirring time of 20 minutes/h, and washing pH of 3. With an irradiation time of 210 min, diazinon degradation reached 90%. [ABSTRACT FROM AUTHOR]

Bioassays based on the determination of acetylcholinesterase (AChE) activity are used for the detection and neurotoxicity evaluation of organophosphate insecticides. However, AChE bioassays are convenient for oxo and iso forms, whereas the limits of detection (LODs) of thio forms, being used as commercial insecticide preparations are significantly higher. In this study various malathion concentrations (1 × 10–9–5 × 10–4 mol/L) were treated with the oxidizing agent, N-bromosuccinimide (NBS) in concentration ratios: 1 : 1, 1 : 2, 1 : 10, and 1 : 20 to find efficient oxidation resulting in as possible as lower LODs of the used assays based on electric eel AChE (20 min-preincubation) and immobilized AChE incorporated in flow-injection analysis (FIA) system. Malathion–NBS ratio of 1 : 10 was found as the most efficient and resulted in a decrease of LOD about 100 times for both AChE bioassays. In the case of free AChE the obtained LOD values after the NBS-induced oxidation of thioorganophosphates (1 : 10), malathion, diazinon, and chlorpyrifos were as follows: 1.0 × 10–8, 1.3 × 10–8, and 1.0 × 10–8 mol/L, respectively. In addition, LOD values for the FIA-AChE system involving a pre-step with NBS induced the following LOD values: 7.2 × 10–7, 1.3 × 10–6, and 1.8 × 10–7 for malathion, diazinon, and chlorpyrifos, respectively. Furthermore, IC50 values of the corresponding oxo forms were found to be similar to those for the studied thioorganophosphates, which indicates a potential stoichiometric conversion of the thio to oxo forms under the established oxidation conditions. [ABSTRACT FROM AUTHOR]

A new pretreatment method termed ultrasound-assisted extraction (UAE) which is combined with solid-phase extraction which is combined with dispersive liquid-liquid microextraction (SPE-DLLME) followed by gas chromatography-flame ionization detector (GC-FID) analysis has been developed for the determination of diazinon in garden parsley as vegetable samples. The analyte was extracted from garden parsley sample using ultrasound-assisted extraction followed by solid-phase extraction followed by dispersive liquid-liquid microextraction. Various parameters that affect the efficiency of the extraction techniques have been optimized. The calibration plot was linear in the range of 5.0–1,000 μg kg−1 with detection limit of 1.0 μg kg−1 for diazinon in garden parsley samples. The results confirm the suitability of the UAE-SPE-DLLME-GC-FID as a sensitive method for the analysis of the targeted analyte in garden parsley samples. [ABSTRACT FROM AUTHOR]

Background: Cholinesterase is a biomarker for poisonings by anticholinesterase agents, but its reference values are scarce, and possible interaction with collars containing parasiticides has not been studied. Objectives: We aimed to evaluate the serum cholinesterase activity of healthy dogs without a history of contact with anticholinesterase agents and healthy animals exposed to commercial collars containing organophosphate. Methods: Ninety‐nine dogs were used and included healthy animals without recent exposure to anticholinesterase agents and healthy animals previously exposed to diazinon collars. Serum quantification of the enzyme butyrylcholinesterase (BuchE) through spectrophotometry was conducted on all samples. In experiment 1, BuchE activity was quantified at time 0 and 7 days after, a time when the samples were kept at −18°C. In experiment 2, sampling times were 0, 7, 14, 21, 28, and 56 days. Results: Time 0 values were 4622.38 ± 1311.53 U/L. After 7 days, a significant decay was observed, with a mean of 3934.45 ± 1430.45 U/L. Spearman's test was performed, finding a weak correlation between ALT, creatinine, total plasma proteins, age, weight, red blood cells, platelets, leukocytes, and BuchE activities. In experiment 2, the mean at time 0 was 4753 ± 454.8 U/L. With exposure to the collar, there was a decay of up to 93% after 14 days. Conclusions: Normality values of serum BuchE in healthy dogs without a history of exposure to anticholinesterase agents were 4360.8–4883.96 U/L. Freezing serum caused a decrease in BuchE activity. Exposure to commercial collars containing diazinon also reduced BuchE activity without clinical signs, indicating that previously exposed animals should be evaluated carefully. [ABSTRACT FROM AUTHOR]