Penconazole Research Articles

Elicitor-enhanced steroidal sapogenin accumulation in hairy root cultures of Trigonella foenum-graecum

In current work, we studied hairy root induction in Trigonella foenum graecum, which is an important medicinal plant, and examined the impact of different elicitors on some phytochemical characteristics and metabolites production in hairy root cultures. Accordingly, some factors such as five strain types of Agrobacterium rhizogenes (1724, 15834, A4, A13 and MSU) and three different explants, namely leaf, cotyledon and hypocotyl were studied. The results showed that different A. rhizogenes strains exhibited different infection efficiency. MSU and 15834 had highest efficiency of hairy root induction than other strains. Also, hairy root induction frequency in leaf explants was higher than in other explants. Salicylic acid (SA), nitric oxide (NO), CaCl2 and penconazole (PEN) were used in elicitation process. Hairy roots were treated with SA (0.1 and 0.5 mM), NO (10 and 50 µM), CaCl2 (5 and 10 mM) and PEN (5 and 10 mg/L). Applied elicitors enhanced antioxidant enzymes activities and reduced oxidative stress markers; this observation might be ascribed to regulation of the oxidative status of the elicited cells. Significant increase of antioxidant metabolites (total phenol, flavonoid and anthocyanin) in PEN-treated hairy roots was associated to phenylalanine ammonia lyase activity, indicating an up-regulation of phenylpropanoid/flavonoid metabolism. PEN and CaCl2 treatment enhanced steroidal sapogenin in hairy root cultures. These results suggested that use of elicitors can enhance the production of secondary metabolites in transformed hairy roots. Among the elicitors applied, CaCl2 and PEN were the most effective in increasing secondary metabolite production in transformed hairy roots of T. foenum graecum.

Neuroprotective effect of Withania somnifera leaves extract nanoemulsion against penconazole-induced neurotoxicity in albino rats via modulating TGF-β1/Smad2 signaling pathway

Penconazole (PEN) is a systemic triazole fungicide used to control various fungal diseases on grapes, stone fruits, cucurbits, and strawberries. Still, it leaves residues on treated crops after collection with many hazardous effects on population including neurotoxicity. Withania somnifera leaves extract (WSLE) is known for its memory and brain function enhancing ability. To evoke such action efficiently, WSLE bioactive metabolites are needed to cross the blood–brain barrier, that could limit the availability of such compounds to be localized within the brain. Therefore, in the present study, the association between PEN exposure and neurotoxicity was evaluated, and formulated WSLE nanoemulsion was investigated for improving the permeability of the plant extract across the blood–brain barrier. The rats were divided into five groups (n = 6). The control group was administered distilled water, group II was treated with W. somnifera leaves extract nanoemulsion (WSLE NE), group III received PEN, group IV received PEN and WSLE, and group V received PEN and WSLE NE. All rats were gavaged daily for 6 weeks. Characterization of compounds in WSLE using LC–MS/MS analysis was estimated. Neurobehavioral disorders were evaluated in all groups. Oxidative stress biomarkers, antioxidant enzyme activities, and inflammatory cytokines were measured in brain tissue. Furthermore, the gene expression patterns of GFAP, APP, vimentin, TGF-β1, Smad2 and Bax were measured. Histopathological changes and immunohistochemical expression in the peripheral sciatic nerve and cerebral cortex were evaluated. A total of 91 compounds of different chemo-types were detected and identified in WSLE in both ionization modes. Our data showed behavioral impairment in the PEN-treated group, with significant elevation of oxidative stress biomarkers, proinflammatory cytokines, neuronal damage, and apoptosis. In contrast, the PEN-treated group with WSLE NE showed marked improvement in behavioral performance and histopathological alteration with a significant increase in antioxidant enzyme activity and anti-inflammatory cytokines compared to the group administered WSLE alone. The PEN-treated group with WSLE NE in turn significantly downregulated the expression levels of GFAP, APP, vimentin, TGF-β1, Smad2 and Bax in brain tissue. In conclusion, WSLE NE markedly enhanced the permeability of plant extract constituents through the blood brain barrier to boost its neuroprotective effect against PEN-induced neurotoxicity.

Protective effects of N-acetyl-l-cysteine against penconazole-triggered hepatorenal toxicity in adult rats.

Penconazole (PEN) is a widely applied triazole fungicide. This study sought to define the efficacy of N-acetyl-l-cysteine (NAC) in mitigating PEN-triggered hepatorenal toxicity in rats. Twenty-eight adult male albino Wistar rats were assigned to four groups: a normal control (NC), a PEN group, a NAC group and a PEN+NAC group. Administration of PEN (50 mg/kg body weight (b.w.) every 2 days) and NAC (150 mg/kg b.w., daily) took place via oral gavage for 10 days. Effective amelioration by NAC of PEN-induced liver and kidney dysfunction was indicated by a significant reduction in the circulating liver and kidney markers (aspartate aminotransferase, alanine aminotransferase, urea and creatinine). Attenuation of PEN-induced oxidative stress and lipid peroxidation in liver and kidney tissues was evident in a significant reduction in malondialdehyde and enhanced total antioxidant capacity. Moreover, NAC significantly reduced the histopathological alterations and the expression of tumour necrosis factor α in liver and kidney tissue. Furthermore, NAC maintained the messenger RNA levels of nuclear factor erythroid 2-related factor 2 (Nrf2), haem oxygenase 1, and Kelch-like erythroid cell-derived protein 1 and prevented nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) protein upregulation caused by PEN. N-acetyl-1-cysteine protected against PEN-induced hepatorenal oxidative damage and inflammatory response via activation of Nrf2 and inhibition of NF-κB pathways.

The study of the removal of penconazole fungicide from surface water using carboxymethyl tragacanth-based hydrogel grafted with poly (acrylic acid-co-acrylamide)

In this study, a polymeric adsorbent based on carboxymethyl tragacanth (CMT) grafted by poly acrylic acid-co-acrylamide (AAc-co-AAm) synthesized by radical polymerization for the first time was used to remove the fungicide penconazole (PEN) or Topas 20% from surface water. The parameters of solution pH, adsorption isotherm, and adsorption kinetics of PEN were studied by the synthetic adsorbent. The surface morphology and functional groups of CMT-g-poly (AAc-co-AAm) were confirmed by XRD, SEM and FT-IR techniques. Adsorption of PEN on CMT-g-poly (AAc-co-AAm) follows the Freundlich and pseudo-second-order models. The significant maximum adsorption capacity of the synthesized polymer was found to be 196.08 mg/g. The synthetic adsorbent had good reproducibility in PEN removal for up to 5 cycles. CMT-g-poly (AAc-co-AAm) is a cost-effective and non-toxic adsorbent for the decontamination of surface water from pesticides.

Application of catalytic hydrodechlorination for the fast removal of chlorinated azole pesticides in drinking water

Catalytic hydrodechlorination (HDC) is regarded as a promising purifying technology for drinking water treatment. So far, it has proved to be highly effective for the removal of different groups of chlorinated micropollutants including pharmaceuticals, neonicotinoid pesticides, personal care products or chloroacetic acids. The azole pesticides, recently included in the EU Watch Lists (Decisions 2020/1161 and 2022/1307), are a group of micropollutants of particular concern for drinking water given their high toxicity, persistence, and bioaccumulation potential. In this work, the feasibility of HDC for the removal of a representative group of chlorinated azole pesticides tebuconazole (TEB), tetraconazole (TET), prochloraz (PCZ), penconazole (PEN), metconazole (MET) and imazalil (IMZ)) is demonstrated, and their reactivity is compared with that observed for other halogenated micropollutant groups. Notably, all the pesticides investigated in this work (100 μg L−1) were completely dechlorinated within 30 min under ambient conditions using a 1 wt% Pd/Al2O3 catalyst concentration of 0.25 g L−1 and a H2 feeding of 50 mL N min−1. The experimental data were accurately described by a pseudo-first order kinetic equation and rate constant values in the range from 1.08 to 2.60 L gcat−1 min−1 were obtained. These values are quite close to those achieved for the most reactive neonicotinoid pesticides and significantly higher than the obtained for chloroacetic acids and most pharmaceuticals (e.g. diclofenac, sertraline or chlorpromazine). From the identification of the generated reaction intermediates and the final non-chlorinated products, sequential reaction pathways were proposed for each pollutant. Remarkably, despite the high toxicity exhibited by the azole pesticides tested, with LC50 values within the 0.4–7.0 mg L−1 range using A. salina, HDC effluents were non-toxic in all cases. Furthermore, the catalyst showed a remarkable stability upon three consecutive runs. Finally, the versatility of the process was demonstrated in the treatment of real aqueous matrices such as DWTP and tap water, where no significant differences were found either in terms of activity or stability.

A dual-state-emission chalcone-based supramolecular probe for ratiometric detection of penconazole in environmental samples

Penconazole (PEN) is a systemic triazole fungicide widely pulverized on fruits and vegetables to control powdery mildew disease. PEN has various hazardous effects on mammalians primarily through PEN-induced excessive generation of reactive oxygen species, which may cause metabolic disorders, cancer, etc. Therefore, development of an effective analytical method for PEN is of great importance for the environmental safety and human health. In the present work, we report a supramolecular fluorescent probe OPyCH@ALB constructed by selecting of a dual-state-emission chalcone as the indicator and albumin as the host, for the first time, successfully realizing the ratiometric detection of PEN. This probe is capable of detecting PEN with rapid response (10 s), high sensitivity (LOD = 0.28 μM, 76 ppb), high selectivity, and a visible fluorescence color change from green to red. Based on this probe, the portable paper-based test strips, which enable the on-site monitoring of PEN without the involvement of any complicated testing apparatus, were fabricated. Furthermore, this probe was used to realize the qualitative and quantitative analysis of PEN in ground water and soil with high accuracy, and successful achieved on-site recognition of PEN on the surface of grapes. We expect that this method will be applied as a convenient and affordable tool for the rapid monitoring of PEN at the point-of-use, such as in residential, agricultural, and food production settings.

Emerging Contaminants Decontamination of WWTP Effluents by BDD Anodic Oxidation: A Way towards Its Regeneration

Electrochemical oxidation using a boron-doped diamond anode (EO-BDD) was tested to remove emerging contaminants commonly present in wastewater treatment plant effluents (WWTPe). The main objective of the work was the regeneration of this water for its possible reuse in high-quality demanding uses. In the first part of the work, we investigated the potential of this technique for removing a group of neonicotinoid pesticides (thiamethoxam (TMX), imidacloprid (ICP), acetamiprid (ACP), and thiacloprid (TCP)) in a WWTP effluent. The influence of operating variables, such as current density, the conductivity of media, supporting electrolyte type (Na2SO4, NaCl or NaNO3), or the natural aqueous matrix on target variables were fully established. Selected target variables were: (1) the percentage of pollutant removal, (2) the kinetics (apparent pseudo-first-order kinetic rate constant), (3) total organic carbon (TOC) removal, and (4) the specific energy consumption (SEC). A response surface methodology (RSM) was applied to model the results for all cases. In the paper’s final part, this technology was tested with a more broad group of common emerging pollutants, including some azole pesticides (such as fluconazole (FLZ), imazalil (IMZ), tebuconazole (TBZ), or penconazole (PNZ)), antibiotics (amoxicillin (AMX), trimethoprim (TMP), and sulfamethoxazole (SMX)), and an antidepressant (desvenlafaxine (DVF)). The results confirm the power of this technology to remove this emerging contamination in WWTP effluents which supposes an interesting way towards its regeneration.

Resveratrol ameliorates penconazole-induced cardiotoxicity by inhibition of oxidative stress and apoptosis in zebrafish larvae

Penconazole (PEN) is a typical systemic triazole fungicide with cardiac toxic effects. Resveratrol (RES) is a natural polyphenolic phytochemical with antioxidation properties. This study aimed to investigate if RES could protect against PEN-induced cardiotoxicity and to determine the underlying mechanisms. Zebrafish embryos were exposed to 0, 0.5, 1 and 2 mg/L of PEN from 4 to 96 h post fertilization (hpf) and cardiac developmental toxicity was assessed. Our results showed that PEN decreased hatching rate, survival rate, heart rate and body length, with increased malformation rate and spontaneous movement. PEN induced pericardial edema and abnormal cardiac structure in myl7:egfp transgenic zebrafish, as well as downregulation of cardiac development related genes (nkx2.5, tbx2.5, gata4, noto, and vmhc). In addition, PEN elevated oxidative stress via reactive oxygen species (ROS) accumulation and triggered cardiomyocytic apoptosis by upregulation of p53, bcl-2, bax and caspase 3. These adverse outcomes were counteracted by RES, indicating that RES ameliorated PEN-induced cardiotoxicity by inhibiting oxidative stress and apoptosis in zebrafish. Taken together, this study revealed the important role of oxidative stress in PEN-induced cardiotoxicity and identified dietary RES supplementation as a novel strategy to mitigate its toxicity.

PH-responsive release and washout resistance of chitosan-based nano-pesticides for sustainable control of plumeria rust

Controlled pesticide release in response to environmental stimuli by encapsulating pesticides in a carrier is a feasible approach to improve the effective utilization rate. In this study, pH-responsive release nanoparticles loaded with penconazole (PE) were prepared by ionic cross-linking of chitosan and carboxymethyl chitosan (PE@CS/CMCS-NPs). PE@CS/CMCS-NPs exhibited good washout resistance and wettability properties, increasing the washing resistance of the pesticide by approximately 20 times under continuous washing. The results of the release experiments showed that nanoparticles had adjustable controlled-release characteristics with the change in pH based on the swelling of nanoparticles. The results of spore germination experiments showed that PE@CS/CMCS-NPs enhanced the inhibitory effect under acidic conditions. The field experiment results showed that PE@CS/CMCS-NPs had a better control effect than PE-aqueous solution, extended the duration and slowed down the dissipation of PE. These results indicated that the CS/CMCS-NPs pH-responsive release system has great potential in the development of an effective pesticide formulation.

Gold-based lateral-flow strip for the detection of penconazole in watermelon and cucumber samples

Abstract As a typical triazole fungicide, penconazole (PEN) is widely used in agriculture but has been proven to be toxic. In this study, we designed a new hapten to prepare a highly sensitive and specific anti-PEN monoclonal antibody (mAb) and established a gold nanoparticle-based lateral-flow immunoassay (LFIA) for the detection of PEN residues in watermelon and cucumber. The 50% inhibitory concentration (IC50) of the mAb was 0.42 ng/mL and the LFIA strip had a visual limit of detection (vLOD) of 2.5 ng/g and a cut-off value of 10 ng/g in watermelon and cucumbers. The calculated limit of detection (LOD) of the LFIA strip was 0.36 ng/g for watermelon and 0.29 ng/g for cucumber. The LFIA strip also gave a recovery rate of 92.5%–109.0% for watermelon samples and 92.5%–106.7% for cucumber samples. These results using the LFIA strip are highly consistent with those seen using liquid chromatography–tandem mass spectrometry. Thus our developed LFIA strip represents a potentially reliable tool for the rapid on-site screening for PEN in watermelons and cucumbers.

Bioaccumulation and toxic effects of penconazole in earthworms (Eisenia fetida) following soil exposure.

As an agricultural fungicide, penconazole (PEN) is widely used and has adverse effects on various organisms. In order to evaluate the ecological safety risks of PEN, the bioaccumulation and toxic effects of PEN in earthworms were studied. Specifically, the results show that the biota-sediment accumulation factor (BSAF) of PEN in earthworms reaches its maximum within 1day, and then decreases slowly. It reached its lowest value after 14days of PEN exposure and then rose again. In addition, oxidative stress and metabolic disorder of the earthworm with PEN exposure were assessed. After PEN exposure, the related indicators of oxidative stress involved in the activities of SOD and CAT and the contents of GSH and MDA all changed significantly in earthworms. Moreover, metabolomics analysis of earthworms showed disturbed metabolic profiles following PEN exposure. Respectively, PEN exposure significantly altered the relative abundances of 14 metabolites in earthworms. In general, exposure to PEN caused oxidative stress and metabolic profile disorders of earthworms. The results of this study will be helpful for further evaluation of soil ecological security of PEN.

Differential proteomics: Effect of growth regulators on salt stress responses in safflower seedlings

Productivity of safflower (Carthamus tinctorius L.) is markedly reduced by salt stress. This study is based on analysis of proteins profile of safflower plants treated with 200 mM NaCl, with exogenously applied salicylic acid (SA) and penconazole (PEN), as growth regulators. Plants were investigated through a gel-based proteomic approach, which resulted in the identification of 17 salt-responsive proteins related to different metabolic modifications. Of these, seven different proteins were up or down regulated by both SA and PEN, suggesting the synergistic and antagonistic effects of SA and PEN. The classification of differentially expressed proteins showed that salt-responsive proteins were mainly involved in photosynthesis, ion homeostasis, and oxidative stress response, as well as nitrogen, protein, and carbohydrate metabolism. The identified stress-responsive proteins in this study could pave the way to develop salt tolerance in safflower, thus sustaining its productivity under salinity. In addition, SA and PEN may be considered as a foliar application to ameliorate salinity effects, due to their low price and availability.

Toxicological potential of penconazole on early embryogenesis of white mice Mus musculus in either pre- or post-implantation exposure.

The present investigation was conducted to evaluate the effect of penconazole (PEN) fungicide on early embryogenesis of white mice. In the first experiment, 48 pregnant females were divided into different groups; the first group is control (G1). The second group (G2) was treated daily with PEN (30-, 20-, 10-, 5-mg/kg BW). The third group (G3) was treated with PEN (5-mg/kg BW; day after the other day). The fourth group (G4) was treated with PEN (2.5-mg/kg BW daily) during pre-implantation stage (from the 1st to the 4th day of gestation). The fifth group (G5) was treated with PEN (2.5-mg/kg BW daily) during post-implantation (from the 5th to the 8th day of gestation). The pregnant females were sacrificed at the 14th day of gestation. In the second experiment, 63 pregnant females were classified into control, PEN-treated during pre-implantation period (2.5-mg/kg BW), and PEN-administered during post-implantation period (2.5-mg/kg BW). Each group was sacrificed at stages E6.5, E7.5, E8.5, E9.5, E11.5, E14.5, and E18.5. The high doses of PEN in the first experiment showed failed pregnancy, foetoresorption, and embryo disorganization. High doses of PEN induce alterations in the uterus tissue at the level of histology and immunohistochemistry for the expression of TGFβ2, TNFR2, Caspase 10, and HSP70. The low doses of PEN in the second experiment showed upregulated expression of TGFβ2, TNFR2, Caspase 10, and HSP70 at stages E6.5 and E7.5. In conclusion, PEN was found to alter the suitable uterine environment for proper implantation and development at the levels of histological and immunohistochemical that could create a risk during the full course of embryogenesis.

Penconazole and calcium ameliorate drought stress in canola by upregulating the antioxidative enzymes.

The aim of this research was to gauge the alternations in the lipid peroxidation and antioxidative enzyme activity in two cultivars (cv. RGS003 and cv. Sarigol) of canola under drought stress and drought tolerance amelioration by penconazole (PEN) and calcium (Ca). Plants were treated with different polyethylene glycol (PEG) concentrations (0, 5, 10 and 15%) without or with PEN (15 mg L-1) and Ca (15 mM). The Ca treatment prevented the negative effects of drought on fresh weight (FW) in RGS003 and Sarigol at 5 and 15% PEG respectively. Ca and PEN/Ca treatments caused significant induction in the proline content in Sarigol at 15% PEG; the latter treatment was accompanied by higher glycine betaine (GB), lower malondialdehyde (MDA) and growth recovery. Hydrogen peroxide (HO2) content in Sarigol was proportional to the severity of drought stress and all PEN, Ca and PEN/Ca treatments significantly reduced the H2O2 content. PEN and PEN/Ca caused alleviation of the drought-induced oxidative stress in RGS003. RGS003 cultivar exhibited significantly higher antioxidative enzymes activity at most levels of drought, which could lead to its drought tolerance and lower MDA content. In contrast to that of Sarigol, the activity of catalase and superoxide dismutase (SOD) increased with Ca and PEN/Ca treatments in RGS003 under low stress. The application of PEN and Ca induced significantly P5CS and SOD expression in RGS003 under drought stress after 24 h. Overall, these data demonstrated that PEN and Ca have the ability to enhance the tolerance against the drought stress in canola plants.

Role of Penconazole in salt stress amelioration in Sesamum indicum L.

ABSTRACT Sesame (Sesamum indicum L.) is one of the world’s important oil crops. The aim of the present study was to investigate the effects of salt stress on physiological and biochemical parameters of sesame and assess the improvement of salt tolerance by Penconazole (PEN). Plants were treated with various NaCl concentrations (0, 50, 100, and 200 mM) without or with PEN (15 mg L−1). Salt stress inhibited the growth in sesame. Our results showed sesame plant under salinity used of the enzymatic and non-enzymatic system and compatible osmolytes to overcome on oxidative and osmotic stress, respectively. PEN improved the growth and reduced the negative effects of salinity in sesame. In fact, PEN increased the resistance of this plant under salt stress by improving the antioxidant system and osmotic regulation. Thus, this compound can be used as stress-ameliorating agents in this crop plant.

Different effects of calcium and penconazole on primary and secondary metabolites of Brassica napus under drought

The effects of penconazole (PEN) and calcium (Ca2+) on physiological and biochemical parameters were investigated in two canola cultivars (RGS003 and Sarigol) under water stress. Drought increased protein content in RGS003, but PEN, Ca2+ and PEN-Ca2+ treatment induced protein content in Sarigol. PEN, Ca2+ and PEN-Ca2+ treatment enhanced soluble sugar content in RGS003. In contrast to Sarigol, drought and PEN treatment induced total phenol content in RGS003. Flavonoid content increased by drought, but Ca2+ and PEN-Ca2+ treatment decreased it in both cultivars. Ca2+ and PEN-Ca2+ treatment enhanced tocopherol content in both cultivars under drought stress. Drought stress increased Phenylalanine ammonia-lyase (PAL) activity in Sarigol. PEN-Ca2+ treatment increased relative expression of PAL and its activity in RGS003. Fatty acid composition was modified by drought, PEN and Ca2+. Saturated fatty acid (stearic acid) content declined but unsaturated fatty acid (oleic acid) content enhanced in both cultivars under drought. The application of PEN and Ca2+ decreased unsaturated fatty acids (linoleic and linolenic acid) in RGS003 under drought. According to our results, PEN and Ca2+ changed physiological and biochemical parameters and therefore these compounds are suggested for reductionof the negative effects of drought stress in canola.

Improving Salt Tolerance in Safflower Plants through Exogenous Application of Penconazole

Core Ideas Penconazole decreases the negative effects of salinity in safflower. Penconazole helps safflower to cope with salinity by the regulation of compatible solutes. Penconazole increases the expression of key genes responsible in defense system. Penconazole increases the activity of enzymatic and non‐enzymatic antioxidants. It has been shown that penconazole (PEN) acts as an endogenous signal molecule responsible for inducing stress tolerance in plants. The effect of PEN (15 mg L−1) and sodium chloride (0, 100, and 200 mM NaCl) on some biochemical and molecular responses of safflower (Carthamus tinctorius L.) were studied. Results revealed that K+ and Ca2+ contents, and some growth parameters decreased under salinity however, Na+ content, compatible solutes, H2O2 and malondialdehyde (MDA) levels, phenolic compounds, phenylalanine ammonia‐lyase (PAL) gene expression, and antioxidant enzyme activities increased. The exogenous PEN had a positive effect on K+ and Ca2+ contents, growth parameters, compatible solutes, antioxidant enzyme activities, and H2O2 content, but decreased Na+ and MDA contents. In addition, quantitative real‐time (qRT)‐polymerase chain reaction (PCR) analysis showed that exogenous PEN induced expression of PAL gene in both untreated and salt‐treated plants. Our data indicate that PEN helps safflower plants to better cope with salt stress. The results provide new insights to mechanisms that help regulate salinity resistance in safflower. Penconazole may be considered as a foliar application to ameliorate salinity effects, due to its low price and availability.

Assessment of penconazole exposure in winegrowers using urinary biomarkers

Penconazole (PEN) is a fungicide used in agriculture. The aim of this work was to evaluate the exposure to PEN in vineyard workers focusing on urinary biomarkers.Twenty-two agricultural workers were involved in the study; they were investigated during PEN applications and re-entry work, performed for 1–4 consecutive working days, for a total of 42 mixing and applications and 12 re-entries. Potential and actual dermal exposure, including hand exposure, were measured using pads and hand washes. Urine samples were collected starting before the first application, continuing during the work shift, and ending 48 h after the last shift. The determination of PEN in dermal samples and PEN metabolites in urine was performed by liquid chromatography tandem mass spectrometry.Dermal potential body exposure and actual total exposure showed median levels ranging from 18 to 3356µg and from 21 to 111 µg, respectively. Urinary monohydroxyl-derivative PEN-OH was the most abundant metabolite; its excretion rate peaked within 24 h after the work shift. In this period, median concentrations of PEN-OH and the carboxyl-derivative PEN-COOH ranged from 15.6 to 27.6 µg/L and from 2.5 to 10.2 µg/L, respectively. The concentration of PEN-OH during the work shift, in the 24 h after and in the 25–48 h after the work shift were correlated with actual body and total dermal exposure (Pearson's r from 0.279 to 0.562).Our results suggest that PEN-OH in the 24 h post-exposure urine is a promising candidate for biomonitoring PEN exposure in agricultural workers.

Penconazole and calcium improves drought stress tolerance and oil quality in canola

ABSTRACTIn this study, the effects of penconazole (PEN) and calcium (Ca) on growth amelioration and quality of seed oil in canola (Brassica napus L.) under drought stress were investigated. Drought stress reduced the growth parameters (fresh weight and dry weight) in canola; however the application of PEN and Ca improved these parameters under drought condition. Inducing effect of Ca on protein content was more prominent than PEN. Proline content increased under drought stress and PEN and Ca treatment caused more induction it under drought. PEN and Ca alleviated the negative effects of drought stress in canola by inducing antioxidant defense. The application of PEN and Ca caused a significant reduction in lipid peroxidation and hydrogen peroxide and mitigation of the drought induced oxidative stress. Drought stress induced protein content, total phenol, flavonol content, soluble sugar, palmitic acid and palmitoloic acid, and reduced flavonoid content, oleic acid, linolenic acid, and linolonoic acid in canola seed. PEN and Ca increased palmitic acid, linoleic acid (Omega-6), linolenic acid (Omega-3), oleic acid, protein, and soluble sugar. Our results indicated that application of PEN and Ca enables canola plants to withstand the deleterious impact of drought stress and caused improvement of antioxidant capacity, essential fatty acids (linolenic acid and linolonoic acid) and oil quality in canola seed.

Determination of tebuconazole and penconazole fungicides in rat and human hair by liquid chromatography/tandem mass spectrometry.

Tebuconazole (TEB) and penconazole (PEN) are widely applied fungicides and environmental contaminants; their toxicological properties include possible effects to the unborn child, therefore, the evaluation of human exposure is relevant to risk assessment. Hair is a non-invasive specimen that incorporates pollutants allowing an extended exposure window to be surveyed. The aim of this work was to develop and validate an assay for the determination of TEB and PEN in human hair. Under optimised conditions, analytes were extracted by soaking hair in acetonitrile, in the presence of deuterated analogues, under heating and agitation. Chemical separation was achieved using a C18 reversed-phase chromatographic column and detection and quantification were performed, after positive electrospray ionization, by triple quadrupole mass spectrometry operating in selected reaction monitoring mode. The assay validation showed a linear dynamic range up to 5μg/L or 200pg/mg hair, inter- and intra-run precisions <6%, and accuracies within 5% of spiked concentrations. Limits of quantification were 0.001μg/L or 1pg/mg hair for both TEB and PEN. Matrix effect experiments showed that the isotope dilution approach allowed for the control of bias sources. TEB and PEN were determined in hair of rats exposed to a low dose of TEB and in hair of agricultural workers exposed to TEB and/or PEN during the application season, indicating that both chemicals are incorporated into the hair upon exposure. The results of this study indicate that the developed assay is useful to evaluate the exposure to TEB and PEN in humans.