ABSTRACT
BACKGROUND: The topical veterinary drug product containing fipronil and permethrin provides an effective repellent protection and high insecticidal efficacy for dogs. OBJECTIVE: The objective of this study was to develop a stability-indicating high-performance liquid chromatography (HPLC) method for simultaneous detection and quantification of fipronil, permethrin, their key degradation products, and butylated hydroxytoluene (BHT) in a topical drug product. METHOD: The two active ingredients, their degradation products, and the antioxidant (BHT) were separated by a gradient elution on a Phenomenex Kinetex C18 column (150 × 3 mm, 2.6 µm particle size) maintained at 37°C with H2O acetonitrile isopropyl alcohol 85% H3PO4 (65.5 + 32.5 + 4/0.0053, v/v/v/v) as mobile phase A and acetonitrile (100%) as mobile phase B. The flow rate was 0.9 mL/min, and analytes were detected and quantified at 235 nm. RESULTS: The specificity of the method was demonstrated by adequate separation of fipronil, permethrin, their degradation products, and BHT in the forced degraded finished product. The linearity of the method was demonstrated in the range of 0.2% to 150% of target analytical concentration of both active ingredients and 50% to 150% for BHT. Excellent recoveries of fipronil, permethrin, and BHT in placebo spiked active ingredient solutions in the linearity range showed sufficient accuracy of the method. The LOQ and LOD of the method were determined to be 0.2% and 0.07% of the analytical concentration. A robustness study did not identify any critical parameter that adversely affected the separation and quantification. CONCLUSIONS: Here, we report the development and validation of a robust, stability-indicating HPLC method for identification and assay of fipronil, permethrin, and BHT, including estimation of fipronil's and permethrin's degradation products in a topical drug product for dogs. HIGHLIGHTS: The new HPLC method permits the acquisition of data for all analytes of interest for a topical finished drug product containing fipronil, permethrin, and BHT.
Subject(s)
Permethrin , Pyrazoles , Permethrin/analysis , Permethrin/chemistry , Chromatography, High Pressure Liquid/methods , Pyrazoles/analysis , Pyrazoles/chemistry , Insecticides/analysis , Drug Stability , Veterinary Drugs/analysis , Administration, Topical , Limit of Detection , AnimalsABSTRACT
Pyrethroid, a pesticide widely used worldwide, could mimic, block, or synergize the effects of endogenous hormones in humans or mammals after entering into the atmosphere and after being sprayed and applied in large quantities. This research aims to study the mechanism, kinetics, and eco-toxicity evaluation of the ozonolysis of permethrin (PER)-one of the typical pyrethroid (type I) pesticides. Existing experimental studies only predicted that ozonolysis of PER could generate a cycloperoxy analogue of PER (IM13-1-11), and the reaction mechanism has not yet been completed. To make up for the lack of experimental results, the 13 primary reaction pathways of PER and ozone, as well as the subsequent reactions of Criegee intermediates with small molecules such as NOx, COx, SO2, and O2, have been studied to propose new reaction paths by quantum chemical calculations in this work. We calculated the total reaction rate constant of PER and ozone at 298 K and 1 atm based on the calculated thermodynamic data and the transition state theory (TST), which was compared with the experimental values to prove the reliability of our results. Based on the quantitative structure and activity relationship, we predicted the acute and chronic toxicity of PER and its products of ozonolysis to three representative organisms-fish, daphnia, and green algae to avoid animal experiments. The results show that ozonolysis products of PER are still extremely harmful to the environment and should be taken seriously, although the products have less toxicity than PER.
Subject(s)
Atmosphere/chemistry , Ozone/chemistry , Permethrin/chemistry , Permethrin/toxicity , Humans , Kinetics , Reproducibility of Results , ThermodynamicsABSTRACT
Permethrin (PM) is one of the chiral insecticides most widely used around the world. The significant differential toxicity of its four enantiomers and its important adverse effects on human health highlights the need for determination of PM enantiomers. The aim of this work was to develop the first enantioselective method for quantification of PM in fruits and vegetables. The method is based on the extraction of PM enantiomers in supramolecular solvents with restricted access properties (SUPRAS-RAM) and their separation/detection by chiral liquid chromatography-tandem mass spectrometry (LC-MS/MS) which is first reported in this article. SUPRAS-RAM-based extraction is proposed as an innovative treatment approach that drastically reduces solvent consumption and avoids the need for sample cleanup. Extraction of PM enantiomers is quick (vortexing for 5 min) and efficient (recoveries 93-107%). The method is sensitive (quantification limits from 1.0 to 1.2 µg kg-1) and suitable for control of PM enantiomers in agri-food products.
Subject(s)
Chromatography, High Pressure Liquid/methods , Food Contamination/analysis , Fruit/chemistry , Insecticides/chemistry , Permethrin/chemistry , Tandem Mass Spectrometry/methods , Vegetables/chemistry , Sensitivity and Specificity , StereoisomerismABSTRACT
Environmental factors, including high temperature and humidity, can influence dermal absorption of chemicals. Soldiers can be dermally exposed to permethrin while wearing permethrin-treated uniforms. This study aimed at examining the effects of high temperature and a combined high temperature and humid environment on permethrin absorption compared with ambient conditions when wearing a permethrin-treated uniform. Twenty-seven male enlisted soldiers wore study-issued permethrin-treated army uniforms for 33 consecutive hours in three different environments: 1) simulated high temperature (35°C, 40% relative humidity [rh]) (n = 10), 2) simulated high temperature and humidity (30°C, 70% rh) (n = 10), and 3) ambient conditions (13°C, 60% rh) (n = 7). Spot urine samples, collected at 21 scheduled time points before, during, and after wearing the study uniforms, were analyzed for permethrin exposure biomarkers (3-phenoxybenzoic acid, cis- and trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylic acid) and creatinine. Biomarker concentrations were 60-90% higher in the heat and combined heat/humidity groups (P < 0.001-0.022) than the ambient group. Also, the average daily permethrin dose, calculated 12 hours after removing the treated uniforms, was significantly higher in the heat (P = 0.01) and the heat/humidity (P = 0.03) groups than the ambient group. There were no significant differences in biomarker concentrations or computed average daily dose between the heat and the heat/humidity groups. Both hot and combined hot and humid environmental conditions significantly increased permethrin absorption in soldiers wearing permethrin-treated uniforms.
Subject(s)
Humidity , Insecticides/urine , Military Personnel , Permethrin/urine , Protective Clothing , Temperature , Adolescent , Biomarkers/urine , Humans , Insecticides/chemistry , Insecticides/pharmacokinetics , Male , Occupational Exposure , Permethrin/chemistry , Permethrin/pharmacokinetics , Time Factors , United States , Young AdultABSTRACT
We developed a method to quantify cis-permethrin and trans-permethrin and their metabolites in several biological matrices in pregnant rats and foetuses using liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS). The objective was to quantify cis-permethrin and trans-permethrin in faeces, kidney, mammary gland, fat and placenta in mothers and in both maternal and foetal blood, brain and liver. The metabolites cis-3-(2,2-dichlorovinyl)-2,2-dimethyl-(1-cyclopropane) carboxylic acid (cis-DCCA), trans-3-(2,2-dichlorovinyl)-2,2-dimethyl-(1-cyclopropane) carboxylic acid (trans-DCCA) and 3-phenoxybenzoic acid (3-PBA) were measured in blood, liver and urine. Sample preparation was performed by liquid-liquid extraction. A purification step was not carried out except for the more complex biological samples (fat, mammary glands and faeces). Validation parameters including specificity, linearity, matrix effect, limits of quantification (LOQs), accuracy and precision were evaluated. The recoveries of target compounds ranged from 47 to 136%. LOQs were in the range 4 to 80 ng/mL for permethrin isomers and 4 to 800 ng/mL for their respective metabolites. Intra- and inter-batch precision and accuracy in matrix were better than 15%. The validated method was applied in a preliminary toxicokinetic study in pregnant rats with oral dosing of 50 mg/kg permethrin. In pregnant rats, permethrin isomers and their metabolites were quantified in all requested matrices except maternal liver and blood for trans-permethrin and cis-DCCA respectively. In foetuses, cis- and trans-permethrin were also quantified, demonstrating that the method is suitable for the analysis of foetal distribution of permethrin in toxicokinetic studies.
Subject(s)
Chromatography, Liquid/methods , Fetus/metabolism , Insecticides/pharmacokinetics , Permethrin/pharmacokinetics , Tandem Mass Spectrometry/methods , Animals , Female , Isomerism , Male , Permethrin/chemistry , Pregnancy , Rats , Rats, Sprague-DawleyABSTRACT
The majority of residents of the United States, Canada, and Europe are exposed to pyrethroids, the most commonly used class of insecticides. Surprisingly little is known about key aspects of their pharmacokinetics, including their mode of transport in the systemic circulation. This study tested the hypothesis that pyrethroids are transported by both plasma lipoproteins and proteins, similarly to other highly lipophilic environmental contaminants. Other aims were to characterize the binding of representative type I and II pyrethroids, and to compare their binding to rat versus human plasma. Binding of 14C-labeled cis-permethrin (CIS), trans-permethrin (TRANS) and deltamethrin (DLM) to proteins and lipoproteins was measured by sequential extraction of spiked plasma with isooctane, 2-octanol, and acetonitrile. Binding of DLM, CIS, and TRANS to plasma proteins and lipoproteins was linear from 250 to 750 nM; concentrations present in the plasma of orally dosed rats. Binding of DLM to high-density lipoprotein was twice that to low-density lipoprotein. Binding of DLM, CIS, and TRANS was â¼2-fold greater to proteins than to lipoproteins of rat and human plasma; albumin was primarily responsible for protein binding. Higher total binding of each pyrethroid to human (â¼90%) than to rat (â¼80%) plasma resulted from higher protein binding in human plasma. This was attributable in part to the higher albumin/protein content of human plasma. Rat albumin exhibited lower pyrethroid binding capacity than did human albumin. The results of this investigation indicate that albumin and lipoproteins play a major role in binding and transport of pyrethroids in the systemic circulation of both rats and humans.
Subject(s)
Blood Proteins/metabolism , Environmental Pollutants/pharmacokinetics , Insecticides/pharmacokinetics , Lipoproteins/metabolism , Administration, Oral , Adult , Animals , Brain/metabolism , Environmental Pollutants/administration & dosage , Environmental Pollutants/chemistry , Environmental Pollutants/toxicity , Humans , Insecticides/administration & dosage , Insecticides/chemistry , Insecticides/toxicity , Male , Nitriles/administration & dosage , Nitriles/chemistry , Nitriles/pharmacokinetics , Nitriles/toxicity , Permethrin/administration & dosage , Permethrin/chemistry , Permethrin/pharmacokinetics , Permethrin/toxicity , Protein Binding , Pyrethrins/administration & dosage , Pyrethrins/chemistry , Pyrethrins/pharmacokinetics , Pyrethrins/toxicity , Rats , Stereoisomerism , Tissue Distribution , Toxicity Tests, AcuteABSTRACT
The rising threat of vector-borne diseases and environmental pollution has instigated the investigation of nanotechnology-based applications. The current study deals with a nanotechnological application involving the usage of nanometric pesticides such as permethrin nanoemulsion. The mean droplet diameter and zeta potential of the prepared permethrin nanoemulsion were found to be 12.4⯱â¯1.13â¯nm and -20.4⯱â¯0.56â¯mV, respectively. The temporal stability of permethrin nanoemulsion was found to be 4 days when checked in the external environment. The permethrin nanoemulsion exhibited LC50 values of 0.038 and 0.047â¯mgL-1 and 0.049 and 0.063â¯mgL-1 against larval and pupal stages of Culex tritaeniorhynchus and Aedes aegypti, respectively. The results obtained from the larvicidal and pupicidal assay were corroborated with the histopathological and biochemical profiles of hosts upon treatment with nanometric pesticide. Further, the biosafety studies of the nanopesticide were carried out against different non-target species like freshwater algae (Closterium), Cicer arietinum (Chickpea) and Danio rerio (Zebrafish), and the mosquitocidal concentration of nanopesticide was found to be non-toxic. The following study, therefore, describes the mosquitocidal efficacy of nanometric pesticide formulated in a greener approach, which can become a substitute for conventional pesticide application in an eco-benign manner.
Subject(s)
Aedes/drug effects , Culex/drug effects , Insecticides/chemistry , Mosquito Vectors/drug effects , Nanostructures/chemistry , Permethrin/chemistry , Animals , Colloids , Emulsions , Insecticides/pharmacology , Insecticides/toxicity , Larva/drug effects , Lethal Dose 50 , Nanostructures/toxicity , Permethrin/pharmacology , Permethrin/toxicity , Plant ExtractsABSTRACT
Permethrin (PER), a type I pyrethroid, is the most widely used insecticide in domestic settings in the United States. The overall objective of this study was to assess the efficiency of the blood-brain barrier (BBB) as an obstacle to the 14C-cis-permethrin (CIS) and 14C-trans-permethrin (TRANS) isomers of PER, and to determine whether its barrier function changes during maturation of the rat. Experiments were conducted to quantify brain uptake of CIS and TRANS in postnatal day 145, 21, and 90 Sprague-Dawley rats. The common carotid artery of anesthetized rats was perfused for 2 or 4 minutes with 1, 10, or 50 µM 14C-CIS or 14C-TRANS in 4% albumin. Brain deposition of each isomer was inversely related to age, with levels in the youngest animals >5 times those in adults. Brain uptake was linear over the 50-fold range of pyrethroid concentrations, indicative of passive, nonsaturable BBB permeation. The extent of uptake of toxicologically relevant concentrations of CIS and TRANS was quite similar. Thus, dissimilar BBB permeation does not contribute to the greater acute neurotoxic potency of CIS, but greater permeability of the immature BBB to CIS and TRANS may contribute to the increased susceptibility of preweanling rodents to the insecticides.
Subject(s)
Blood-Brain Barrier/metabolism , Insecticides/pharmacokinetics , Permethrin/pharmacokinetics , Age Factors , Animals , Animals, Newborn , Dose-Response Relationship, Drug , Female , Insecticides/chemistry , Insecticides/toxicity , Male , Models, Animal , Permeability , Permethrin/chemistry , Permethrin/toxicity , Rats , Rats, Sprague-Dawley , Stereoisomerism , Toxicity Tests, AcuteABSTRACT
The metabolism of the pyrethroids deltamethrin (DLM), cis-permethrin (CPM) and trans-permethrin (TPM) was studied in human expressed cytochrome P450 (CYP) and carboxylesterase (CES) enzymes. DLM, CPM and TPM were metabolised by human CYP2B6 and CYP2C19, with the highest apparent intrinsic clearance (CLint) values for pyrethroid metabolism being observed with CYP2C19. Other CYP enzymes contributing to the metabolism of one or more of the three pyrethroids were CYP1A2, CYP2C8, CYP2C9*1, CYP2D6*1, CYP3A4 and CYP3A5. None of the pyrethroids were metabolised by CYP2A6, CYP2E1, CYP3A7 or CYP4A11. DLM, CPM and TPM were metabolised by both human CES1 and CES2 enzymes. Apparent CLint values for pyrethroid metabolism by CYP and CES enzymes were scaled to per gram of adult human liver using abundance values for microsomal CYP enzymes and for CES enzymes in liver microsomes and cytosol. TPM had the highest and CPM the lowest apparent CLint values for total metabolism (CYP and CES enzymes) per gram of adult human liver. Due to their higher abundance, all three pyrethroids were extensively metabolised by CES enzymes in adult human liver, with CYP enzymes only accounting for 2%, 10% and 1% of total metabolism for DLM, CPM and TPM, respectively.
Subject(s)
Carboxylesterase/chemistry , Cytochrome P-450 Enzyme System/chemistry , Nitriles/chemistry , Permethrin/chemistry , Pyrethrins/chemistry , Carboxylesterase/metabolism , Cytochrome P-450 Enzyme System/metabolism , Humans , Nitriles/pharmacokinetics , Permethrin/pharmacokinetics , Pyrethrins/pharmacokinetics , StereoisomerismABSTRACT
BACKGROUND: In a recent article in The Lancet, Protopopoff et al. stated that insecticide resistance must be tackled and concluded that adding the insecticide synergist piperonyl butoxide (PBO) to a bed net with a pyrethroid as principal insecticide might be a part of the response. MAIN TEXT: The study in Tanzania compares malaria prevalence between users of two different nets with the principal insecticide permethrin: Olyset and Olyset Plus (Olyset+), the latter also holding the synergist molecule PBO, the first not. The article is based on randomized cluster trial of very high quality, but Olyset+ exposes much more permethrin at the surface so the higher efficacy may not be because of the added PBO. CONCLUSION: Data published by the World Health Organization (WHO) when evaluating Olyset+ as well of the study of Protopopoff et al. showed that much more permethrin is available on the surface of Olyset+ than on the surface of Olyset and the relatively small and rapidly dwindling dosage of PBO may have nothing to do with the superior effect of Olyset+. The WHO should not change politics for "PBO nets" based on this study alone.
Subject(s)
Insecticide-Treated Bednets , Malaria/prevention & control , Humans , Insecticides/analysis , Insecticides/chemistry , Permethrin/analysis , Permethrin/chemistry , Randomized Controlled Trials as Topic , Tanzania , World Health OrganizationABSTRACT
While most hair care formulations are developed on the basis of surfactants or polymers, we introduce self-assembly coating of micro and nanoparticles as the underlying principle for hair modification, protection and enhancement. Halloysite clay nanotubes formed by rolled sheets of aluminosilicate kaolin assemble on the surface of hair forming a robust multilayer coverage. Prior to the application, clay nanotubes were loaded with selected dyes or drug allowing for hair coloring or medical treatment. This facile process is based on a 3-minute application of 1 wt% aqueous dispersion of color/drug loaded halloysite resulting in a ca. 3 µm thick uniform hair surface coating. This technique, which employs a very safe, biocompatible and inexpensive material, is ubiquitous with respect to the species of source of hair and additives in solvent, making it viable as an excipient for conventional medical and veterinarian formulations.
Subject(s)
Aluminum Silicates/chemistry , Cosmetics/chemistry , Hair/chemistry , Nanotubes/chemistry , Animals , Caenorhabditis elegans/anatomy & histology , Clay , Coloring Agents/chemistry , Drug Compounding , Drug Liberation , Hair/ultrastructure , Hydrophobic and Hydrophilic Interactions , Nanotubes/ultrastructure , Permethrin/chemistry , Permethrin/pharmacology , Toxicity TestsABSTRACT
Insecticides used in the agriculture and forestry have side effects on non-target organisms used as natural enemies. This study evaluated the histopathology and cytotoxicity of permethrin on the midgut of the non-target predatory bug, Podisus nigrispinus (Heteroptera: Pentatomidae) used in the biological control of pest insects. The toxicity and survival of this insect were determined using six concentrations of permethrin via ingestion. Histological and ultraestutural changes of the midgut of P. nigrispinus were analyzed after exposure to permethrin. The insecticide caused toxicity in P. nigrispinus with LC50â¯=â¯0.46⯵gâ¯L-1 and survival of 47% after 72â¯h of exposure. The histological changes in the midgut were irregularly bordered epithelium, cytoplasmic vacuolization and apocrine secretions in the lumen after 6â¯h following exposure to the insecticide. Cytotoxic effects such as granules and vacuoles secreted into the lumen, presence of autophagosomes, and dilatation of infolds of the basal plasma membrane were observed in the three regions of the midgut. Cells of the midgut in apoptosis occurred after 12â¯h of exposure. Permethrin causes toxic effects, inhibits survival, and produces changes in the histology and cytology of the midgut in P. nigrispinus, suggesting that the cell stress induced by this insecticide can disrupt physiological processes such as digestion, compromising the potential of the predator as a biological control agent of pests. The low selectivity of permethrin to a non-target organism such as the predatory bug, P. nigrispinus indicates that the associated use of this insecticide in biological control should be better evaluated.
Subject(s)
Digestive System/drug effects , Permethrin/chemistry , Animals , HeteropteraABSTRACT
Permethrin is a type I (noncyano) pyrethroid that induces tremors at high concentrations and increases acoustic startle responses (ASRs) in adult rodents, however its effects in young rats have been investigated to a limited extent. ASR and tremor were assessed in adult and postnatal day (P)15 Sprague-Dawley rats at oral doses of 60, 90, or 120 mg/kg over an 8 h period. Permethrin increased ASR in adults, regardless of dose, and 20% of the high-dose rats showed tremor at later time points. For the P15 rats all doses induced tremor at all time points, and ASR was increased at 2 h in the 90 and 120 mg/kg groups with a trend in the 60 mg/kg group compared with controls. The 60 mg/kg group showed increased ASR at 4 and 6 h, whereas the 90 mg/kg group showed no differences from the controls at these times. The 120 mg/kg group showed decreased ASR from 4- to 8-h posttreatment. P15 and adult rats both showed plasma and brain cis- and trans-permethrin increases after dosing. After the same dose of permethrin, P15 rats had greater cis- and trans-permethrin in brain and plasma compared with adults. P15 rats had an increased tremor response compared with adults even at comparable brain permethrin concentrations. For ASR, P15 rats responded sooner and showed a biphasic pattern ranging from increased to decreased response as a function of dose and time, unlike adults that only showed increases. Overall, young rats showed greater effects from permethrin compared with adults.
Subject(s)
Brain/drug effects , Insecticides/toxicity , Permethrin/toxicity , Reflex, Startle/drug effects , Acoustic Stimulation , Age Factors , Animals , Animals, Newborn , Brain/growth & development , Brain/metabolism , Dose-Response Relationship, Drug , Female , Insecticides/blood , Insecticides/chemistry , Male , Permethrin/blood , Permethrin/chemistry , Rats , Rats, Long-Evans , Rats, Sprague-Dawley , StereoisomerismABSTRACT
Glutathione S-transferases (GSTs) are a family of enzymes that function in the detoxification of variety of electrophilic substrates. In the present work, we report a novel zeta-like GST (designated as KKSG9) from the biphenyl/polychlorobiphenyl degrading organism Acidovorax sp. KKS102. KKSG9 possessed low sequence similarity but similar biochemical properties to zeta class GSTs. Functional analysis showed that the enzyme exhibits wider substrate specificity compared to most zeta class GSTs by reacting with 1-chloro-2,4-dinitrobenzene (CDNB), p-nitrobenzyl chloride (NBC), ethacrynic acid (EA), hydrogen peroxide, and cumene hydroperoxide. The enzyme also displayed dehalogenation function against dichloroacetate, permethrin, and dieldrin. The functional role of Tyr12 was also investigated by site-directed mutagenesis. The mutant (Y12C) displayed low catalytic activity and dehalogenation function against all the substrates when compared with the wild type. Kinetic analysis using NBC and GSH as substrates showed that the mutant (Y12C) displayed a higher affinity for NBC when compared with the wild type, however, no significant change in GSH affinity was observed. These findings suggest that the presence of tyrosine residue in the motif might represent an evolutionary trend toward improving the catalytic activity of the enzyme. The enzyme as well could be useful in the bioremediation of various types of organochlorine pollutants.
Subject(s)
Bacterial Proteins/chemistry , Comamonadaceae/enzymology , Glutathione Transferase/chemistry , Tyrosine/chemistry , Amino Acid Sequence , Bacterial Proteins/genetics , Catalysis , Dieldrin/chemistry , Enzyme Activation , Gene Expression , Glutathione Transferase/genetics , Kinetics , Molecular Docking Simulation , Mutagenesis, Site-Directed , Permethrin/chemistry , Pesticides/chemistry , Substrate SpecificityABSTRACT
A sensitive method for the simultaneous determination of cis-permethrin (cis-PERM) and trans-permethrin (trans-PERM) in small volumes (100µL) of rat plasma and brain homogenate was developed, using a liquid-liquid extraction for sample preparation and gas chromatography-negative chemical ionization mass spectrometry (GCNCI-MS) for detection. Quantitation of trace levels of the insecticide in small volumes of biological samples is essential to support toxicokinetic studies in small animals. There are currently no validated methods in the literature for determining cis-PERM and trans- PERM in volumes as low as 100µL of rat plasma or brain homogenate. The method provided a linear range of 0.2-150.0ng/mL for analytes in both matrices. The intra- and inter-batch precision (as% relative standard deviation, RSD) and accuracy (as relative error, RE) of the method were better than 20% at the limit of quantitation and better than 15% across the remaining linear range. The validated method was applied in a toxicokinetic study in adult rats with oral dosing of 10mg/kg (cis-PERM) and 100mg/kg (trans-PERM) in corn oil. cis-PERM and trans- PERM were monitored in rat plasma and brain tissue samples for 6h following dosing, and both analytes were detected in all plasma and brain samples.
Subject(s)
Brain Chemistry/physiology , Gas Chromatography-Mass Spectrometry/methods , Permethrin/analysis , Animals , Linear Models , Liquid-Liquid Extraction/methods , Male , Permethrin/blood , Permethrin/chemistry , Rats , Rats, Sprague-Dawley , Reproducibility of Results , Sensitivity and SpecificityABSTRACT
Permethrin, the most widely used household insecticide in the United States, is marketed as a mixture of its cis (CIS) and trans (TRANS) isomers. The major objective of this investigation is to develop and utilize a reliable approach to determine in vivo partition coefficients (PCs) for CIS and TRANS in immature and adult Sprague-Dawley rats. Adult, postnatal day (PND) 21, and PND 15 rats were infused with environmentally relevant concentrations of CIS or TRANS via a subcutaneous osmotic pump for 48 or 72 h. The adult and PND 21 rats also received an oral loading dose. Systemic steady-state or equilibrium was attained in each age group within 72 h of the protocol. CIS and TRANS were both distributed to tissues according to their neutral lipid content, with adipose tissue exhibiting much higher tissue:plasma PCs than skeletal muscle, liver, or brain. Liver:plasma and brain:plasma PCs were consistently at or lower than unity. Tissue:plasma PCs were generally higher for CIS than for TRANS, although the isomers are of comparable lipophilicity. Significantly higher blood levels of CIS apparently saturate plasma binding, resulting in greater tissue deposition of the isomer. CIS and TRANS tissue:plasma PCs were found to be inversely related to the rats' age, although TRANS brain:plasma PCs were comparable in immature and mature animals. These data support the conclusion that age-dependent partitioning is an important determinant of the pharmacokinetics of permethrin. Such partitioning could influence the risk assessment of these insecticides in infants and children when incorporated into physiologically based pharmacokinetic models.
Subject(s)
Enzyme Inhibitors/pharmacokinetics , Insecticides/pharmacokinetics , Permethrin/pharmacokinetics , Animals , Enzyme Inhibitors/administration & dosage , Enzyme Inhibitors/blood , Enzyme Inhibitors/chemistry , Female , Insecticides/administration & dosage , Insecticides/blood , Insecticides/chemistry , Isomerism , Male , Permeability , Permethrin/administration & dosage , Permethrin/blood , Permethrin/chemistry , Rats, Sprague-Dawley , Tissue DistributionABSTRACT
The present work was designed to study the mechanisms associated with Nurr1 modulation following early life permethrin (PERM) treatment during rat's life span. Here we demonstrate that PERM exposure in rats, at a dose close to No Observed Adverse Effect Level (NOAEL) for 15days during neonatal brain development leads to its accumulation long after exposure. In striatum from adolescent rats we detected an increase in DNA methyltransferases (DNMTs) such as DNMT1, DNMT3a, Tyrosine hydroxylase, monomeric and aggregated α-synuclein protein levels. Adult rats showed enhanced DNMT3b and α-synuclein aggregation compared to the control group, while with aging a significant decrease in all biomarkers studied was observed. No changes in Nurr1 promoter methylation in adolescent, adult and old rats were found. In silico studies showed clear evidence of a strong binding interaction between PERM and its metabolite 3-phenoxybenzoic acid with the nuclear orphan receptor Nurr1. These findings suggest that an additional interference with the dopaminergic neuron pathway could occur in situ during PERM accumulation in brain. Therefore, Nurr1 modulation in early life PERM-treated rats, depends on age-related adaptive responses in animals.
Subject(s)
Corpus Striatum/drug effects , Corpus Striatum/diagnostic imaging , Nuclear Receptor Subfamily 4, Group A, Member 2/metabolism , Permethrin/toxicity , Aging/metabolism , Animals , Benzoates/chemistry , Benzoates/metabolism , Binding Sites , Corpus Striatum/metabolism , DNA Methylation/drug effects , DNA Modification Methylases/metabolism , Male , Molecular Docking Simulation , Molecular Dynamics Simulation , Nuclear Receptor Subfamily 4, Group A, Member 2/genetics , Permethrin/chemistry , Permethrin/metabolism , Promoter Regions, Genetic , Protein Multimerization , Rats, Wistar , alpha-Synuclein/metabolismABSTRACT
Nanopesticides such as nanopermethrin can serve as an alternative to conventional pesticides causing eco-toxicity. The nanoformulation of this pyrethroid pesticide was carried out by solvent evaporation of pesticide-loaded microemulsion. The Z average for the nanopermethrin dispersion in paddy field water was found to be 169.2 ± 0.75 nm with a polydispersity index of 0.371 that exhibits uniform dispersion. Further, the nanopermethrin (NP) dispersion exhibited an effective stability in the paddy field water for a duration of 48 h with a Z average of 177.3 ± 1.2 nm and a zeta potential of -30.7 ± 0.9 mV. The LC50 of the nanopermethrin against Culex tritaeniorhynchus in the field condition was found to be 0.051 µg/mL. In addition to the stability assessment, the biosafety of the nanopermethrin was commenced on the beneficial bacterial isolate Enterobacter ludwigii (VITSPR1) considered as plant growth-promoting rhizobacteria. The toxic effect of nanopesticide was compared to its bulk counterpart, i.e. bulk permethrin (BP) at a concentration of 100 µg/mL, and the nanopesticide was found to be potentially safe. The results of biomarker enzymatic assays (lipid peroxidase, glutathione reductase, lactate dehydrogenase) displayed insignificant (p < 0.05) toxicity of NP towards the bacterial cells compared to BP. The live-dead cell staining and SEM analysis illustrated negligible toxicity of NP towards the bacteria. The non-toxic behaviour of the NP towards the non-target species was studied which displayed the eco-safe property of NP.
Subject(s)
Enterobacter/drug effects , Nanostructures/chemistry , Oryza/microbiology , Permethrin/pharmacology , Pesticides/pharmacology , Rhizome/microbiology , Animals , Culex/growth & development , Enterobacter/enzymology , Enterobacter/growth & development , Fresh Water/chemistry , Lethal Dose 50 , Lipid Peroxidation/drug effects , Oryza/growth & development , Oxidative Stress/drug effects , Particle Size , Permethrin/chemistry , Permethrin/toxicity , Pesticides/chemistry , Pesticides/toxicity , Rhizome/growth & development , Soil MicrobiologyABSTRACT
Pyrethroids and metals were simultaneously detected in aquatic environment and showed antagonistic lethality to the benthic invertebrate, Chironomus dilutus. Accelerated biotransformation of pyrethroids in organism by the presence of metals was proposed as the likely reason for the antagonism. Mechanistic explanation for the role of toxicokinetics of pyrethroids in the antagonistic interaction would help better understanding the reasons for the joint toxicity. The goal was achieved in the current study by evaluating the impact of cadmium on toxicokinetic parameters of permethrin in C. dilutus, and by explaining the interaction through quantifying the activity and gene expression of biotransformation-related enzymes. Toxicokinetic parameters were simulated using a first-order kinetic model. Bioconcentration factors and uptake and elimination rate constants for permethrin were not significantly changed with the addition of cadmium at sublethal level, neither did the activity of enzymes, including glutathione S-transferase (GST), carboxylesterase (CarE), catalase and lipid peroxidation. Yet, the activities of metabolism-related enzymes (GST and CarE) showed an elevating tendency with adding cadmium. Furthermore, the expression of metabolism-related genes, including cytochrome P450 and glutathione S-transferase genes were significantly up-regulated in C. dilutus exposed to a mixture of permethrin and cadmium compared with permethrin only. Although co-exposure to cadmium did not induce toxicokinetic changes of permethrin in C. dilutus, it did enhance the activity of metabolic enzymes which were encoded by the metabolism-related genes, suggesting an acceleration of biotransformation of permethrin to less toxic metabolites in the midges. This possibly explained the antagonistic interaction for permethrin and cadmium.
Subject(s)
Cadmium/chemistry , Cadmium/metabolism , Chironomidae/metabolism , Insecticides/pharmacology , Permethrin/chemistry , Permethrin/pharmacology , Water Pollutants, Chemical/metabolism , Animals , Biotransformation , Carboxylesterase/metabolism , Catalase/metabolism , Gene Expression/drug effects , Glutathione Transferase/metabolism , Lipid Peroxidation/physiology , ToxicokineticsABSTRACT
The heterogeneous reactions of gas-phase ozone and two pyrethroid pesticides, deltamethrin and permethrin, which are the most frequently applied insecticides today, has been investigated. Tentative identifications of heterogeneous ozonolysis products of both pesticides reveal that the reaction mechanisms differ and are mainly influenced by the presence of the cyano moiety at the α-position of deltamethrin (pyrethroid type II). The mechanism study also suggests the important role of water. Finally, several of the degradation products emerged from the ozonolysis of deltamethrin and permethrin may pose further health and environmental hazard due to their higher toxicity, such as phosgene for permethrin, and bromophosgene, 3-phenoxybenzaldehyde (3-PBA) and fulminic acid for deltamethrin. The results obtained in this study can contribute to better describe the atmospheric fate of pesticides in the particle phase.