-
Environmental Monitoring and Assessment May 2023In this study, the degradation of two organophosphate pesticides, namely, propetamphos and azamethiphos, in the presence of Ag at different mole ratios was investigated....
In this study, the degradation of two organophosphate pesticides, namely, propetamphos and azamethiphos, in the presence of Ag at different mole ratios was investigated. Moreover, the kinetic and degradation pathways of both chemicals in the range of 0-60 min were explored. Gas chromatography equipped with a thermionic specific detector was used to investigate the pesticide degradation kinetics and mechanism. The results show that the degradation rate of both pesticides follows first-order kinetic. The first-order rate constant and the half-life of reaction were in the range of 0.002-0.143 min, 187-2.1 min, and 0.005-0.164 min and 60-1.8 min, for propetamphos and azamethiphos, respectively, at ambient temperature (25 ºC). Because group containing sulfur atom is a better leaving group than group containing nitrogen, the rate of degradation of azamethiphos is higher than propetamphos. In a higher mole ratio of Ag to pesticides, the degradation rate was increased, and it is possible to predict the rate of degradation of pesticides according to the chemical composition of leaving group.
Topics: Silver; Environmental Monitoring; Pesticides
PubMed: 37249693
DOI: 10.1007/s10661-023-11356-w -
Food and Chemical Toxicology : An... Jul 2010The present study was conducted to investigate the effectiveness of propolis in alleviating the toxicity of propetamphos on haematological and biochemical parameters in...
The present study was conducted to investigate the effectiveness of propolis in alleviating the toxicity of propetamphos on haematological and biochemical parameters in rats. Twenty-four female Wistar-Albino rats (200-250 g) were randomly divided into four equal groups of six rats each. As normal drinking water was given to the control group, propolis (100 mg/kg bw/day), propetamphos (15 mg/kg bw/day), and propolis (100 mg/kg bw/day) with propetamphos (15 mg/kg bw/day) combinations were given to the other three groups by adding to drinking water for 28 days, respectively. The levels of glucose and triglyceride, and the activities of aspartate aminotransferase (AST), alkaline phosphatase (ALP), and alanine aminotransferase (ALT) were increased, and total protein was decreased in serum of rats treated with propetamphos. Lymphocyte percentage was increased, while neutrophil percentage and total leukocyte counts were decreased due to propetamphos administration. In conclusion, propetamphos was determined to cause harmful effects in rats, and the administration of propolis to these animals alleviated the harmful effects of propetamphos.
Topics: Animals; Blood Chemical Analysis; Female; Gas Chromatography-Mass Spectrometry; Insecticides; Leukocyte Count; Liver Function Tests; Organothiophosphorus Compounds; Propolis; Protective Agents; Rats; Rats, Wistar
PubMed: 20385195
DOI: 10.1016/j.fct.2010.04.010 -
Journal of Biochemical Toxicology 1992Propetamphos [(E)-1-methylethyl 3-[[(ethylamino)methoxyphosphinothioyl]oxy]-2-butenoate], the active ingredient in Safrotin, is an organophosphate developed by Sandoz,... (Comparative Study)
Comparative Study
Propetamphos [(E)-1-methylethyl 3-[[(ethylamino)methoxyphosphinothioyl]oxy]-2-butenoate], the active ingredient in Safrotin, is an organophosphate developed by Sandoz, Ltd. (Switzerland) as an insecticide (1). Although metabolism of propetamphos has been previously investigated (2,3), there is no pharmacokinetic data available in the literature. The current studies were undertaken to investigate the pharmacokinetics of propetamphos following intravenous administration in male and female Fischer 344 (F344) rats. Rats were dosed via an indwelling jugular cannula at a dose of 12 mg/kg (one-tenth the oral LD-50). Blood samples were withdrawn via the cannula at predetermined timepoints to quantitate plasma concentrations of propetamphos over time. Propetamphos is highly bound to plasma proteins (free fraction = 0.06). Free propetamphos concentration in plasma vs. time data were analyzed by noncompartmental methods. The terminal elimination rate constant, lambda, was significantly different for males versus females (0.015 min-1 for males and 0.037 min-1 for females, p = 0.001). Plasma was cleared of unbound propetamphos at rates of 0.559 +/- 0.069 and 0.828 +/- 0.181 L/min/kg for males and females (mean +/- standard error). Mean residence times (MRTs) for propetamphos in the body for males and females were 28.3 +/- 5.7 and 14.4 +/- 3.5 min, and the volume of distribution at steady state (Vss) was 14.7 +/- 2.6 and 12.3 +/- 4.5 L/kg. The differences in these parameters, clearance (CI), MRT, and Vss, were not statistically significant at the p < 0.05 level for males versus females, but MRT was nearly significantly different (p = 0.08).(ABSTRACT TRUNCATED AT 250 WORDS)
Topics: Animals; Blood Proteins; Female; Injections, Intravenous; Insecticides; Male; Organothiophosphorus Compounds; Protein Binding; Rats; Rats, Inbred F344; Sex Factors
PubMed: 1293308
DOI: 10.1002/jbt.2570070402 -
Drug and Chemical Toxicology Nov 2022The aim of this study was to investigate the protective efficacy of chrysin against propetamphos exposure. For this purpose, 2 to 3-month-old 40 male Wistar Albino rats...
The aim of this study was to investigate the protective efficacy of chrysin against propetamphos exposure. For this purpose, 2 to 3-month-old 40 male Wistar Albino rats were used. These animals were randomly assigned to four groups. The animals in the control group received the vehicle substance (corn oil) alone. Groups 2, 3 and 4 were administered with 50 mg/kg.bw/day of chrysin (in corn oil), 10 mg/kg.bw/day of propetamphos (in corn oil), and 10 mg/kg.bw/day of propetamphos plus 50 mg/kg.bw/day of chrysin, respectively, for 28 days. Some oxidative stress/lipid peroxidation parameters (MDA, SOD, CAT, GSH-Px, NO, glutathione) and serum biochemical parameters (triglyceride, cholesterol, creatinine, BUN, creatine phosphokinase, ALT, ALP and pseudocholinesterase) were analyzed in tissue/blood samples. Also, histopathological findings were observed. According to the data obtained, no significant alteration had occurred in these parameters and the histological findings in the group given chrysin alone, when compared to the control group. Significant unfavorable alterations were detected in the oxidative stress/lipid peroxidation/antioxidant status parameters, all biochemical parameters and histopathological findings of the group that received propetamphos alone. In the group that was given both chrysin and propetamphos, remedial/recovery alterations were observed in the oxidative stress/lipid peroxidation/antioxidant status values, serum biochemical parameters and histopathological findings, such that the values and histopathological findings showed partly similarity to those of the control group. In result, it is suggested that chrysin may provide protection against propetamphos exposure and propetamphos-induced organ damage in rats at a certain level.
Topics: Animals; Male; Rats; Antioxidants; Butyrylcholinesterase; Corn Oil; Creatine Kinase; Creatinine; Glutathione; Lipid Peroxidation; Liver; Oxidative Stress; Rats, Wistar; Superoxide Dismutase; Triglycerides
PubMed: 34587847
DOI: 10.1080/01480545.2021.1981479 -
Environmental Toxicology and... Mar 2011The present study aimed at defining the testicular toxicity of propetamphos. Mature male albino rats (5-6 months old) were treated with propetamphos orally at doses of...
The present study aimed at defining the testicular toxicity of propetamphos. Mature male albino rats (5-6 months old) were treated with propetamphos orally at doses of 0, 0.18, 0.38, 0.75, 1.5 and 3mg/kg/day for 60 consecutive days. Propetamphos at a dose of 0.38 mg/kg/day significantly reduced the sperm motility only. At 0.75 mg/kg/day sperm count, sperm motility, plasma testosterone level and activity of sorbiol dehydrogenase (SDH) were significantly reduced and sperm morphological abnormalities were significantly increased. At 1.5mg/kg/day weight of testes, seminal vesicle and epididymis were reduced dose dependently whereas, at 3mg/kg/day, weight of prostate gland and activities of acid phosphatase (ACP) and glucose-6-P-dehydrogenase (G6PDH) were decreased significantly. On histopathological examination indicated toxicity of propetamphos on testes depending on dose and observed at doses higher than 0.38 mg/kg/day. These results indicate testicular toxicity of propetamphos at dose of 0.38 mg/kg/day or higher in male albino rats.
Topics: Acid Phosphatase; Animals; Body Weight; Genitalia, Male; Glucosephosphate Dehydrogenase; Insecticides; L-Iditol 2-Dehydrogenase; Male; Organ Size; Organothiophosphorus Compounds; Rats; Sperm Count; Sperm Motility; Spermatozoa
PubMed: 21787702
DOI: 10.1016/j.etap.2011.01.001 -
Veterinary Parasitology May 2009Hard tick infestation is an important problem in both traditional and industrial animal husbandry as well as in veterinary and public health. Several acaricides have...
Hard tick infestation is an important problem in both traditional and industrial animal husbandry as well as in veterinary and public health. Several acaricides have been used to control tick infestation in Iran. Poor control has been attributed to acaricide resistance in tick populations although this has not been demonstrated experimentally. In this study, susceptibility status to propetamphos (Blotic) of 2-3-week-old larvae of Rhipicephalus bursa, one of the most common tick species in Iran, was evaluated using the FAO recommended larval packet test (LPT) method with some modifications. Log dosage probit analysis of propetamphos dose-response regression lines produced a resistance ratio based on LC(50) in the most resistant strain of approximately 103-fold. Biochemical assays suggested that the tick strains contained multiple insecticide resistance mechanisms involving elevation of esterases, GSTs, MFOs and alteration of acetylcholinesterase. In light of this data, practical implications for pest and pesticide resistance management strategies are discussed.
Topics: Animals; Insecticide Resistance; Insecticides; Iran; Organothiophosphorus Compounds; Rhipicephalus
PubMed: 19286323
DOI: 10.1016/j.vetpar.2009.02.005 -
Toxicology Letters Aug 2002Propetamphos ((E)-O-2-isopropylcarbonyl-1-methylvinyl-O-methylethyl phosphoramidothioate) is an organophosphate pesticide (OP) and has been used as an active ingredient...
Propetamphos ((E)-O-2-isopropylcarbonyl-1-methylvinyl-O-methylethyl phosphoramidothioate) is an organophosphate pesticide (OP) and has been used as an active ingredient in sheep dip where there is the potential for significant dermal exposure during dipping. Biological monitoring of exposure to propetamphos has until recently relied on the measurement of cholinesterase activity in plasma. Following the development of a novel method for the determination of propetamphos metabolites in urine, it is now possible to biologically monitor exposure using urine samples. This paper describes a human volunteer study involving oral and dermal exposure to propetamphos.
Topics: Administration, Cutaneous; Administration, Oral; Adult; Environmental Monitoring; Female; Humans; Insecticides; Male; Middle Aged; Occupational Exposure; Organothiophosphorus Compounds
PubMed: 12191868
DOI: 10.1016/s0378-4274(02)00179-0 -
Environmental Toxicology Nov 2016This study was aimed at determining the acute and chronic toxic effects of cypermethrin, propetamphos, and combined cypermethrin and propetamphos. Four groups, each...
This study was aimed at determining the acute and chronic toxic effects of cypermethrin, propetamphos, and combined cypermethrin and propetamphos. Four groups, each comprising 10 animals, were established for the acute (a) and chronic (b) toxicity trials, and in total, 80 male Wistar albino rats were used. In the acute toxicity trial, the first group was maintained for control purposes, and groups 2a, 3a, and 4a were administered only once with 80 mg/kg.bw of cypermethrin, 25 mg/kg.bw of propetamphos and 80 mg/kg.bw of cypermethrin combined with 25 mg/kg.bw of propetamphos, respectively, by gavage directly into the stomach. In the chronic toxicity trial, the first group was also maintained for control purposes, while groups 2b, 3b, and 4b were administered daily with 12 mg/kg.bw of cypermethrin, 4 mg/kg.bw of propetamphos, and 12 mg/kg.bw of cypermethrin combined with 4 mg/kg.bw of propetamphos respectively, by gavage directly into the stomach for 60 days. Blood and tissue (liver, kidney, brain, spleen, and testis) samples were taken 24 h after pesticide administration in the acute toxicity trial and at the end of day 60 in the chronic toxicity trial. Oxidative stress (MDA, NO, SOD, CAT, GSH-Px, and G6PD) parameters, serum biochemical parameters (glucose, triglyceride, cholesterol, HDL, LDL, BUN, creatinine, AST, ALT, ALP, protein, and albumin) and hepatic drug-metabolizing parameters (CYP2E1, CYPB5, CYTC, GST, and GSH) were investigated in the samples. When administered either alone or in combination, both pesticides inhibited the antioxidant enzymes and increased MDA and NO levels. For the drug-metabolizing parameters investigated, particularly in the chronic period, either increase (CYP2E1, CYPB5, and CYTC) or decrease (GST and GSH) was observed. Furthermore, some negative changes were detected in the serum biochemical parameters. In result, cypermethrin and propetamphos combinations and long-term exposure to these combinations produced a greater toxic effect than the administration of these insecticides alone. © 2015 Wiley Periodicals, Inc. Environ Toxicol 31: 1415-1429, 2016.
Topics: Animals; Drug Combinations; Insecticides; Kidney; Liver; Male; Organothiophosphorus Compounds; Oxidative Stress; Pyrethrins; Rats; Rats, Wistar; Testis; Toxicity Tests, Acute; Toxicity Tests, Chronic
PubMed: 25926273
DOI: 10.1002/tox.22147 -
The Science of the Total Environment Aug 2006To quantify the impact of organophosphate pesticides on aquatic ecosystems requires a mechanistic understanding of their behaviour in a range of environmental matrices.... (Comparative Study)
Comparative Study
To quantify the impact of organophosphate pesticides on aquatic ecosystems requires a mechanistic understanding of their behaviour in a range of environmental matrices. The objective of this study was to compare the sorption/desorption, biodegradation and toxic effects of the Pestanal grade and commercial formulation (Ectomort Centenary) of the organophosphate insecticide propetamphos in river and estuarine sediments. For both formulations, the sorption of propetamphos onto sediment was initially very rapid followed by a slower sorption phase. Similarly, the initial rate of desorption was rapid, followed by a much slower rate. In both sorption and desorption experiments, the level of sorbed propetamphos was considerably higher for the commercial formulation of propetamphos (Kd=7-11) than for the Pestanal grade (Kd=4-10). The rate of propetamphos biodegradation was sediment dependent but was most rapid where microbial activity and nutrients were the highest and sorption was the lowest. Propetamphos was more rapidly degraded in sediments under aerobic (t(1/2)=15 d) compared to anaerobic conditions (t(1/2)=19 d). However, no significant difference in the biodegradation rates of the Pestanal grade and commercial formulations of propetamphos were observed. The toxic effect of propetamphos on sediment microbial communities was significantly greater for the commercial formulation than for the Pestanal grade of propetamphos based on EC50 (21 versus 236 microg g(-1)) and EC10 values (0.3 versus 54 microg g(-1)). In conclusion, our results highlight the importance of using commercial pesticide formulations when carrying out ecotoxicological testing.
Topics: Adsorption; Bacteria; Biodegradation, Environmental; Geologic Sediments; Insecticides; Organothiophosphorus Compounds; Rivers; Seawater; Water Pollutants, Chemical
PubMed: 16171848
DOI: 10.1016/j.scitotenv.2005.08.008 -
Journal of Arthropod-borne Diseases Dec 2023Bedbugs are nocturnal ectoparasites that have made a comeback after 20 years and have become one of the main challenges for pest control methods worldwide. Monitoring...
BACKGROUND
Bedbugs are nocturnal ectoparasites that have made a comeback after 20 years and have become one of the main challenges for pest control methods worldwide. Monitoring chemical pesticide resistance is crucial for identifying the best bed bugs management strategies to effectively manage arthropods. This study aims to assess the susceptibility of (Hemiptera: Cimicidae) collected from different parts of Khorasan-Razavi Province, (northeast of Iran) to deltamethrin (pyrethroid), phoxim (organothiophosphate) and propetamphos (phosphoramidate).
METHODS
This study was conducted from Dec 2020 to May 2021. The efficacy of three insecticides (deltamethrin, phoxim, and propetamphos) on adult was assessed using a bioassay method recommended by the World Health Organization (WHO),. Concentrations of deltamethrin used were 10, 20, 40, 80, 160, 320, 640, 1280, and 2560 ppm, while concentrations of phoxim and propetamphos were 10, 40, 160, and 320 ppm. The bed bugs were continuously exposed to the insecticide for 24 hours, and mortality was assessed at regular intervals during the observation period. The concentration-response data were subjected to POLO-PC software and data were analyzed by the one-way and two-way ANOVA procedures.
RESULTS
The lethal concentration fifty values of deltamethrin, phoxim and propetamphos on the examined bed bugs were 0.551, 0.148 and 0.237 ppm, respectively. Insecticide effects of phoxim were significantly higher (P≤ 0.05) compared to each of either deltamethrin and propetamphos agents.
CONCLUSION
The insecticide effects of phoxim against bed bugs were significantly higher compared to each of either deltamethrin or propetamphosinsecticides.
PubMed: 38868674
DOI: 10.18502/jad.v17i4.15299