Search results for "Propoxur"

showing 7 items of 7 documents

Clean analytical method for the determination of propoxur

1995

Abstract A method has been developed for the determination of propoxur, a carbamate pesticide, by means of its reaction with p-aminophenol (PAP). The method involves the reaction, in the presence of KIO4, between the quinoneimine form of PAP and the deprotonated form of 2-isopropoxyphenol, obtained by the alkaline hydrolysis of propoxur, to provide an indophenol dye which absorbs at 600 nm. The analysis is carried out in a flow system and, after the measurement step, the waste, the reaction product and the unreacted derivatising agent is detoxified in a UV-irradiated coil placed after the measurement flow-cell and after mixing the waste with a TiO2(anatase) catalyst slurry, which can be reu…

AnataseChromatographymedicine.diagnostic_testPropoxurAlkaline hydrolysis (body disposal)BiochemistryAnalytical ChemistryCatalysischemistry.chemical_compoundchemistrySpectrophotometrySlurrymedicineEnvironmental ChemistryIndophenolDerivatizationSpectroscopyAnalytica Chimica Acta
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Comparison of basal cytotoxicity of seven carbamates in CHO-K1 cells

2006

The cytotoxic effects of seven carbamate pesticides, aldicarb, aldicarb sulfone, aldicarb sulfoxide, benfuracarb, pirimicarb, propoxur and thiobencarb, were compared in Chinese hamster ovary (CHO-K1) cell line of Circetulus griseus. The endpoints evaluated were lysosomal function by neutral red assay and mitochondrial integrity by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT assay). The carbamates tested were evaluated in both serum-free medium and in serum-containing medium. Results demonstrate that CHO-K1 lysosomes appeared more susceptible to propoxur, aldicarb and its metabolites than mitochondria. Aldicarb was the most toxic carbamate pesticide tested on CHO-K1 cel…

CarbamateNeutral redAldicarbHealth Toxicology and Mutagenesismedicine.medical_treatmentChinese hamster ovary cellPropoxurBiologyPirimicarbPollutionchemistry.chemical_compoundchemistryBiochemistrymedicineEnvironmental ChemistryMTT assayCytotoxicityToxicological & Environmental Chemistry
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Simultaneous Kinetic Determination of Carbamate Pesticides after Derivatization withp-Aminophenol by Using Partial Least Squares

1996

Abstract A method has been developed for the fast spectrophotometric determination of propoxur, carbaryl, and ethiofencarb in water samples using injection analysis in the stopped-flow mode. The method is based on the reaction between p -aminophenol and the phenolic compounds obtained from the pesticides, after a previous hydrolysis with 0.05 M NaOH at room temperature for 15 min. The partial least-squares treatment of the spectrophotometry kinetic data provides a simultaneous determination of the three carbamate pesticides assayed with a relative accuracy error lower than 5% in complex mixtures also containing formetanate, which is only partially hydrolyzed under the experimental condition…

Chromatographymedicine.diagnostic_testPropoxurAnalytical Chemistrychemistry.chemical_compoundHydrolysischemistryFormetanateEthiofencarbSpectrophotometryCarbarylPartial least squares regressionmedicineDerivatizationSpectroscopyMicrochemical Journal
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Flow-injection spectrophometric determination of propoxur with p-aminophenol

1992

Abstract The spectrophotomeric determination of propoxur [2-(1-methyxlthoxy)phenyl methyl carbamate] was carried out with p -aminophenol (PAP) in a flow system. The method involves the on-line hydrolysis with NaOH of propoxur to 2-isopropoxyphenol and the oxidation of PAP to its relative quinone imine with KIO 4 and the reaction between the phenolate and the quinone imine. A four-channel flow manifold was employed to carry out all the different steps of the reaction considered, monitoring the indo dye formed at 600 nm. The developed procedure provides a typical calibration line of A = 0.000 7 + 1.8 × 10 3 C ( A = absorbance; C = concentration in M) with a regression coefficient of 0.9998 an…

Detection limitChromatographyP-AminophenolIminePropoxurBiochemistryAnalytical ChemistryMethyl carbamateQuinoneAbsorbanceHydrolysischemistry.chemical_compoundchemistryEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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Effects of aldicarb and propoxur on cytotoxicity and lipid peroxidation in CHO-K1 cells

2010

Abstract Cytotoxic effects of aldicarb, its sulfone and sulfoxide, and propoxur, lipid peroxidation and antioxidant parameters in Chinese Hamster Ovary (CHO-K1) cells were determined. d , l -buthionine-( S , R )-sulfoximine (BSO) was assayed to determine the role of GSH in the protection against carbamate cytotoxicity. Pre-treatment with 60 μM BSO, induced a significant decrease in the glutathione reductase (GR; 64–141%), the glutathione peroxidase (GPx; 10–30%) and the glutathione S-transferase (GST; 59–93%) activities, and its GSH levels (79–85%), while the oxidized glutathione (GSSG) levels significantly increased (64–78%) respect to experiment non-BSO-pretreated. Carbamates BSO pre-trea…

InsecticidesAntioxidantmedicine.medical_treatmentGlutathione reductaseCHO CellsPharmacologyPropoxurToxicologymedicine.disease_causeAntioxidantsLipid peroxidationchemistry.chemical_compoundCricetulusCricetinaemedicineAnimalschemistry.chemical_classificationGlutathione peroxidaseGeneral MedicineGlutathionePropoxurMalondialdehydeGlutathionechemistryBiochemistryLipid PeroxidationAldicarbOxidative stressFood ScienceFood and Chemical Toxicology
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Effects of four carbamate compounds on antioxidant parameters

2009

Abstract The effect of four carbamates, aldicarb and its metabolites (aldicarb sulfone and aldicarb sulfoxide) and propoxur on glutathione content and the activity of the enzymes involved in the sulfur-redox cycle in the mammalian cellular model CHO-K1 cells after 24-h exposure were determined. Carbamate exposure resulted in a depletion of intracellular reduced glutathione (GSH) content, no change was observed in oxidized glutathione (GSSG) and a decrease in GSH/GSSG ratio was detected. After carbamates exposition a GSH/GSSG decreases in ranged from 12.44% to 21.35% of control was observed. Depletion of GSH levels was accompanied by the induction of glutathione reductase (GR) after 24 h exp…

InsecticidesCarbamateAntioxidantAldicarbHealth Toxicology and Mutagenesismedicine.medical_treatmentGlutathione reductaseCHO CellsPropoxurmedicine.disease_causeAntioxidantschemistry.chemical_compoundCricetulusCricetinaemedicineAnimalschemistry.chemical_classificationGlutathione PeroxidaseGlutathione DisulfideGlutathione peroxidasePublic Health Environmental and Occupational HealthGeneral MedicineGlutathionePropoxurGlutathionePollutionOxidative StressGlutathione ReductasechemistryBiochemistryEnzyme InductionAldicarbOxidative stressEcotoxicology and Environmental Safety
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Use of semipermeable membrane devices for monitoring pesticides in indoor air.

2009

Abstract In this work, 40 pesticides from different categories were analyzed in the air of 20 indoor places that have an intensive use of pesticides. Passive sampling was carried out by using semipermeable membrane devices (SPMDs) deployed for 7 days. SPMDs were analyzed using microwave-assisted extraction and GC/MS. PCB-195 was used as an internal standard. Recoveries ranged between 81 and 108 for many compounds, with RSD values <11. Typical LOD values for 7 days of sampling were from 0.1 to 3.1 ng/m. Propamocarb, propoxur, carbosulfan, pirimicarb, metribuzin, metalaxyl, pendimethalin, oxadiazon, phenothrin, and permethrin were detected in 11 sampling sites, with air concentrations …

Time FactorsPirimicarbChemistry Techniques AnalyticalGas Chromatography-Mass SpectrometryPermeabilityAnalytical Chemistrychemistry.chemical_compoundmedicineEnvironmental ChemistryPesticidesPharmacologyAir PollutantsPesticide residueReproducibility of ResultsMembranes ArtificialEquipment DesignPesticidePropoxurModels TheoreticalchemistryEnvironmental chemistryAir Pollution IndoorCalibrationPropamocarbCarbosulfanPhenothrinAgronomy and Crop ScienceFood SciencePermethrinmedicine.drugEnvironmental MonitoringJournal of AOAC International
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