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At least 199 records · Page 11Linked to original sources
PubMed1991

Development of environmentally compatible controlled release formulations of a mosquito larvicide.

A new controlled release system of a mosquito larvicide, fenthion has been developed by the chemical modification of sodium carboxymethylcellulose into a hydrophobic gel of copper carboxymethylcellulose. Four formulations having a slab geometry were developed with two concentrations of the larvicide and two extents of cross-linking. The release profile of the larvicide from the formulations was studied under laboratory conditions. The formulation with a cross-linking period for 48 h and a 20 per cent larvicide concentration with respect to the dry weight of the formulation has been found to be stable with a sustained release of the active ingredient for a period of 25 wk. The release profile of the formulation followed zero order release kinetics after three weeks in water. The concentration of fenthion ranged between 0.07 and 0.21 mg/l at the application rate of one slab per five litres of water with an average release rate of 6.38 mg/wk during the period of study.

Animals↗
PubMed1985

Laboratory evaluation of four organophosphate compounds as larvicides against field collected salt marsh Culicoides spp. (Diptera: Ceratopogonidae).

The relative effectiveness of 4 organophosphate compounds was tested in the laboratory against Culicoides spp. larvae obtained from salt marsh areas on the Gulf coast of Florida. Larvae were exposed to the insecticide either in estuarine water or in a combination of estuarine water and dried substrate from the salt marsh habitat. The relative potency of the 4 chemicals varied greatly, with chlorpyrifos being the most toxic. Nine times as much temephos, 22 times as much fenthion, and 176 times as much malathion were required to achieve the 50% mortality level compared to chloryprifos (LC50, 0.5 ppb) in water. Addition of habitat soil did not change the order of effectiveness, but 9 times as much chlorpyrifos, 2.3 times as much temephos, and 1.3 times as much fenthion or malathion were required to cause the same mortality as in estuarine water alone.

Animals↗
PubMed1984

Correction of organophosphate-induced neuromuscular blockade by diphenhydramine.

Dogs exposed to topical organophosphate (fenthion) developed decreased plasma and muscle cholinesterase activities. After 2 doses were applied (1 week between doses), plasma concentrations declined 80% and muscle cholinesterase activity was reduced by 56%. Decremental responses to repetitive nerve stimulation developed after fenthion administration. Diphenhydramine, but not placebo, corrected the electrical abnormalities caused by organophosphate application, but without altering plasma or muscle cholinesterase activity. Control dogs housed in the same kennel demonstrated a slight decrease (18%) of plasma cholinesterase, which indicates that there may be potential cross contamination. Diphenydramine may be effective in treating organophosphate-induced neuromuscular weakness which is refractory to other forms of therapy.

Animals↗
PubMed1976

Laboratory insecticide susceptibility tests against Mansonia larvae.

Insecticides Abate, DDT, Dowco-214, Dursban, fenitrothion, fenthion, gamma-HCH, and malathion were tested against the field collected fourth instars larvae of Mansonia from Penang Island, Malaysia. The larvae appeared to be highly susceptible to Dursban and Abate with LC50 values of 1.54 and 1.92 parts per billion respectively. Other chemicals, in decreasing degree of effectiveness, were gamma-HCH, fenthion, P,P'-DDT, Dowco-214, fenithrothion and malathion. The potential use of these chemicals in Mansonia control was discussed. A simple method for collecting and testing Mansonia larvae was also described.

Animals↗
PubMed1995

Resistance in some Caribbean populations of Aedes aegypti to several insecticides.

Thirty-four strains of Aedes aegypti larvae from 17 Caribbean countries were bioassayed for sensitivity to temephos, malathion, fenitrothion, fenthion, and chlorpyrifos. There were fairly high levels of resistance in Tortola (10-12-fold resistance) and Antigua (6-9-fold resistance) strains to temephos and to fenthion (Tortola, 7-10-fold; Antigua, 6-10-fold resistance). Most other strains showed some resistance to malathion, fenitrothion, and chlorpyrifos, but only moderate levels. Adult populations of Ae. aegypti--Aruba, Jamaica, Trinidad, Puerto Rico, St. Lucia, and Antigua strains--also showed moderate resistance to malathion. Mosquito control field data supported the laboratory findings. Doubling the diagnostic dosage of temephos for larval Ae. aegypti was only partially effective against a more resistant strain, and even so, the chemical lost its limited efficacy over a short period of time. Integrated strategies for Ae. aegypti control to mitigate the negative effects of insecticide resistance in the Caribbean strains are suggested.

Aedes↗
PubMed1994

A study of cognitive functions and event related potentials following organophosphate exposure.

To study the cognitive changes following chronic occupational exposure to organophosphate (OP) pesticides, a clinical and neurophysiological study was performed on 31 workers engaged in spraying fenthion, an OP pesticide. The mean age of the workers was 32.1 years (range 19-55) and mean duration of exposure 10.5 years (range 1-14). The workers reported mild transient symptoms after spraying. There was no clinical evidence suggestive of excessive cholinergic activity. Clinical psychometry revealed significant changes in Benton visual retention test, memory quotient, and Alexander's Passalong Test. Serum AChE level was 27% less in the exposed group compared to the controls. P3 of event related potentials were elicited in 28 subjects, P3 latency though was prolonged in one subject only but the group difference was significant. The amplitude of P3 however did not show significant difference. The results suggest subtle subclinical effect of chronic fenthion exposure on the cognitive functions and event related potentials.

Acetylcholinesterase↗
PubMed1981

Recovery of brain and plasma cholinesterase activities in ducklings exposed to organophosphorus pesticides.

Brain and plasma cholinesterase (ChE) activities were determined for mallard ducklings (Anas platyrhynchos) exposed to dicrotophos and fenthion. Recovery rates of brain ChE did not differ between ducklings administered a single oral dose vs. a 2-week dietary dose of these organophosphates. Exposure to the organophosphates, followed by recovery of brain ChE, did not significantly affect the degree of brain ChE inhibition or the recovery of ChE activity at a subsequent exposure. Recovery of brain ChE activity followed the general model Y = a + b(logX) with rapid recovery to about 50% of normal, followed by a slower rate of recovery until normal ChE activity levels were attained. Fenthion and dicrotophos-inhibited brain ChE were only slightly reactivated in vitro by pyridine-2-aldoxime methiodide, which suggested that spontaneous reactivation was not a primary method of recovery of ChE activity. Recovery of brain ChE activity can be modeled for interpretation of sublethal inhibition of brain ChE activities in wild birds following environmental applications of organophosphates. Plasma ChE activity is inferior to brain ChE activity for environmental monitoring, because of its rapid recovery and large degree of variation among individuals.

Animals↗
PubMed1995

Determination of organophosphorus pesticides and their transformation products in river waters by automated on-line solid-phase extraction followed by thermospray liquid chromatography-mass spectrometry.

The trace-level determination of ten priority organophosphorus (OP) pesticides (e.g., chlorpyrifos-methyl, diazinon, disulfoton, fenthion, fenamiphos) and various transformation products (TPs; e.g., disulfoton sulfoxide, fenthion sulfoxide etc.) using automated on-line solid-phase extraction (SPE) with C18 precolumns followed by LC-MS and thermospray interface with time-scheduled selected-ion monitoring (SIM) was developed. Two main ions (usually [M+H]+ and [M+NH4]+ or [M+CH3CN]+) were used for each pesticide in the positive ion (PI) detection mode, while [M-H]- and [M+HCOO]- ions were used in the negative ion (NI) mode. The proposed method requires 100 ml of sample for a limit of detection (LOD) of 0.01-0.1 microgram/l. Calibration graphs were constructed by preconcentrating 100 ml of water spiked with the pesticide mixture at various concentrations (from 0.025 to 2 microgram/l). Good linearity was observed for most of the analytes studied. The experimental setup described in this paper was applied to study the kinetics of degradation of ten organophosphorus pesticides in spiked river water samples. The different samples were first analyzed by an automated on-line precolumn exchange system (OSP-2) followed by LC with diode array detection. To confirm the identity of the organophosphorus pesticides detected, the samples were then analyzed by automated on-line SPE-LC-MS. The method permitted unequivocal identification of many of the TPs formed during the experiments, e.g., the oxo-derivatives of chlorpyrifos-methyl, temephos and pyridafenthion, fenamiphos sulfoxide. Many of these TPs are here reported for the first time since previously used MS-based techniques were not sensitive enough.

Biodegradation, Environmental↗
PubMed1991

The effect of detergents on the purified flavin-containing monooxygenase of mouse liver, kidney and lungs.

1. The effect of various commonly used membrane solubilizing detergents on the activity of the microsomal xenobiotic metabolizing enzyme, the flavin-containing monooxygenase (FMO) purified from mouse liver, kidney and lungs was determined. 2. Regardless of the type of detergent used, the effect on the enzyme activity was variable depending on the type of substrate used. 3. Emulgen 911 concentrations of up to 10% had very little effect on thiobenzamide-S-oxidation by liver, kidney or lung FMO. 4. While Emulgen 911 increased substrate dependent NADPH oxidation rate by thiourea and thioacetamide, it drastically reduced the activity toward the organophosphorous compounds, disulfoton, fenthion, fonofos and phorate at low concentrations. 5. Activities of fenthion, phorate and fonofos were decreased by 80, 65 and 55% by the inclusion of 0.25% Emulgen 911 in the assay mixture. 6. This decline in FMO activity for phorate was evident regardless of the type of detergent used. In contrast, thiourea dependent NADPH oxidation rate in the presence of various detergents was variable. 7. Thiourea oxidation rate was decreased by cholate and Zwittergent 3-12, whereas it was increased in the presence of Emulgen 911, Triton X-100 and Tween 20. 8. This study shows that before FMO activity is determined in the presence of detergents their effects should be carefully evaluated.

Animals↗
PubMed2005

Electrochemical detoxification of four phosphorothioate obsolete pesticides stocks.

The phosphorothioate pesticides are widely used for crop production and fruit tree treatment, but their disposal causes serious environmental problems. Four commercial phosphorothioate pesticides (Demeton-S-methyl, Metamidophos, Fenthion and Diazinon) were treated by an electrolysis system using Ti/Pt as anode and stainless steel 304 as cathode. A number of experiments were run in a laboratory scale pilot plant and the results are presented. For Fenthion the achieved reduction was over 60%, while for Demeton-S-methyl, Metamidophos and Diazinon was more than 50%. Diazinon had the lowest energy demand. The COD/BOD5 ratio was improved considerably after electrolysis for all four pesticides examined. As a conclusion, electrochemical oxidation could be used as a pretreatment method of the pesticides detoxification.

Electrochemistry↗
PubMed2000

Efficacy and safety of selamectin against fleas and heartworms in dogs and cats presented as veterinary patients in North America.

A series of randomized, controlled, masked field studies was conducted to assess the efficacy and safety of selamectin in the treatment of flea infestations on dogs and cats, and in the prevention of heartworm infection in dogs. In addition, observations were made on the beneficial effect of selamectin treatment on dogs and cats showing signs of flea allergy dermatitis (FAD). In all studies selamectin was applied topically, once per month, in unit doses providing a minimum dosage of 6mgkg(-1). Dogs and cats with naturally occurring flea infestations, some of which also had signs associated with FAD, were assigned randomly to receive three months of topical treatment with selamectin (220 dogs, 189 cats) or a positive-control product (dogs: fenthion, n=81; cats: pyrethrins, n=66). Selamectin was administered on days 0, 30, and 60. Day 0 was defined as the day that the animal first received treatment. Flea burdens were assessed by flea comb counts and clinical evaluations of FAD were performed before treatment, and on days 14, 30, 60, and 90. On days 30, 60, and 90, mean flea counts in selamectin-treated dogs were reduced by 92.1, 99.0, and 99.8%, and mean flea counts in fenthion-treated dogs were reduced by 81.5, 86.8, and 86.1%, respectively, compared with day 0 counts. Also, on days 30, 60, and 90, mean flea counts in selamectin-treated cats were reduced by 92.5, 98.3, and 99.3%, and mean flea counts in pyrethrin-treated cats were reduced by 66.4, 73.9, and 81.3%, respectively, compared with day 0 counts. Selamectin also was beneficial in alleviating signs in dogs and cats diagnosed clinically with FAD. A total of 397 dogs free of adult heartworm infection from four heartworm-endemic areas of the USA were allocated randomly to six months of treatment with selamectin (n=298) or ivermectin (n=99). Selamectin achieved a heartworm prevention rate of 100%, with all dogs testing negative for microfilariae and adult heartworm antigen on days 180 and 300. Selamectin was administered to a total of 673 dogs and 347 cats having an age range of 6 weeks to 19 years (3954 doses). The animals included 19 purebred or crossbred Collies (Bearded, Border, and unspecified). There were no serious adverse events. Results of these studies indicated that selamectin was highly effective in the control of flea infestations in dogs and cats without the need for simultaneous treatment of the environment or of in-contact animals and also was beneficial in alleviating signs associated with FAD. Selamectin also was 100% effective in preventing the development of canine heartworms and was safe for topical use in dogs and cats.

Animals↗
PubMed1997

Comparative in vitro and in vivo protein kinase C activation by selected pesticides and transition metal salts.

Various pesticides and transition metals induce oxidative deterioration of biological macromolecules. Protein kinase C (PKC) may mediate these effects. However, no information is available regarding whether these xenobiotics can modulate PKC which is a critical event signaling the increase in endothelial permeability and cell proliferation. Female Sprague-Dawley rats were treated p.o. with two 0.25 LD50 doses of selected pesticides and transition metal salts at 0 and 21 h, and killed at 24 h. PKC activities were measured in liver and brain tissues. Cultured PC-12 cells were incubated for 24 h with 50, 100 or 200 nM concentrations of these pesticides, while 0.20, 0.40 or 0.60 microM concentrations of cadmium chloride (Cd(II)) and sodium dichromate (Cr(VI)) salts were employed. PKC activations were observed in the hepatic and brain cytosol fractions by all xenobiotics. Approximately 1.4- to 2.0-fold and 1.6- to 3.5-fold increases in PKC activity in the hepatic and brain cytosol fractions were observed, respectively. In the hepatic tissues, the greatest increases in activities were observed with TCDD, chlorpyrifos, endrin and Cd(II), while chlorpyrifos and fenthion exerted the greatest increases in the brain tissues. In cultured PC-12 cells, the greatest activation of PKC was observed primarily with 100-nM concentrations of the pesticides. The maximum effects were induced by chlorpyrifos, fenthion, Cd(II) and Cr(VI) salt. The results clearly indicate that pesticides as well as Cd(II) and Cr(VI) salts can modulate a vital component of the cell signaling pathway, namely PKC activity. PKC may be a target of free radicals and oxidative stress, leading to altered cell proliferation and differentiation.

Animals↗
PubMed2000

Pesticide residues in grapes, wine, and their processing products.

In this review the results obtained in the 1990s from research on the behavior of pesticide residues on grapes, from treatment to harvest, and their fate in drying, wine-making, and alcoholic beverage processing are reported. The fungicide residues on grapes (cyproconazole, hexaconazole, kresoxim-methyl, myclobutanil, penconazole, tetraconazole, and triadimenol), the application rates of which were of a few tens of grams per hectare, were very low after treatment and were not detectable at harvest. Pyrimethanil residues were constant up to harvest, whereas fluazinam, cyprodinil, mepanipyrim, azoxystrobin, and fludioxonil showed different disappearance rates (t(1/2) = 4.3, 12, 12.8, 15.2, and 24 days, respectively). The decay rate of the organophosphorus insecticides was very fast with t(1/2) ranging between 0.97 and 3.84 days. The drying process determined a fruit concentration of 4 times. Despite this, the residue levels of benalaxyl, phosalone, metalaxyl, and procymidone on sun-dried grapes equalled those on the fresh grape, whereas they were higher for iprodione (1.6 times) and lower for vinclozolin and dimethoate (one-third and one-fifth, respectively). In the oven-drying process, benalaxyl, metalaxyl, and vinclozolin showed the same residue value in the fresh and dried fruit, whereas iprodione and procymidone resides were lower in raisins than in the fresh fruit. The wine-making process begins with the pressing of grapes. From this moment onward, because the pesticide on the grape surface comes into contact with the must, it is in a biphasic system, made up of a liquid phase (the must) and a solid phase (cake and lees), and will be apportioned between the two phases. The new fungicides have shown no effect on alcoholic or malolactic fermentation. In some cases the presence of pesticides has also stimulated the yeasts, especially Kloeckera apiculata, to produce more alcohol. After fermentation, pesticide residues in wine were always smaller than those on the grapes and in the must, except for those pesticides that did not have a preferential partition between liquid and solid phase (azoxystrobin, dimethoate, and pyrimethanil) and were present in wine at the same concentration as on the grapes. In some cases (mepanipyrim, fluazinam, and chlorpyrifos) no detectable residues were found in the wines at the end of fermentation. From a comparison of residues in wine obtained by vinification with and without skins, it can be seen that their values were generally not different. Among the clarifying substances commonly used in wine (bentonite, charcoal, gelatin, polyvinylpolypyrrolidone, potassium caseinate, and colloidal silicon dioxide), charcoal allowed the complete elimination of most pesticides, especially at low levels, whereas the other clarifying substances were ineffective. Wine and its byproducts (cake and lees) are used in the industry to produce alcohol and alcoholic beverages. Fenthion, quinalphos, and vinclozolin pass into the distillate from the lees only if present at very high concentrations, but with a very low transfer percantage (2, 1, and 0.1%, respectively). No residue passed from the cake into the distillate, whereas fenthion and vinclozolin pass from the wine, but only at low transfer percentages (13 and 5%, respectively).

Food Handling↗
PubMed1998

Genetically engineered broad-spectrum disease resistance in tomato.

Resistance in tomato to the bacterial pathogen Pseudomonas syringae pathovar tomato requires Pto and Prf. Mutations that eliminate Prf show a loss of both Pto resistance and sensitivity to the organophosphate insecticide fenthion, suggesting that Prf controls both phenotypes. Herein, we report that the overexpression of Prf leads to enhanced resistance to a number of normally virulent bacterial and viral pathogens and leads to increased sensitivity to fenthion. These plants express levels of salicylic acid comparable to plants induced for systemic acquired resistance (SAR) and constitutively express pathogenesis related genes. These results suggest that the overexpression of Prf activates the Pto and Fen pathways in a pathogen-independent manner and leads to the activation of SAR. Transgene-induced SAR has implications for the generation of broad spectrum disease resistance in agricultural crop plants.

Journal Article↗
PubMed1985

Toxicity of organophosphorus esters to laying hens after oral and dermal administration.

Fourteen organophosphorus esters (OPs) were evaluated for their potential to cause organophosphorus ester induced delayed neurotoxicity (OPIDN) when administered dermally and/or orally to white leghorn hens. The compounds were chlorpyrifos, DEF, dichlorvos, dimethoate, EPN, ethoprop, fenthion, isofenphos, leptophos, merphos, ronnel, tetrachlorvinphos, terbufos, and trichlorfon. DEF induced ataxia if given dermally or orally at over 21 mg/kg/day for up to 90 days. Hens treated with EPN developed irreversible ataxia after repeated exposure to as little as 1.3 mg/kg dermally or 5 mg/kg/day orally, while leptophos was neurotoxic at doses of 6-7 mg/kg/day dermally and 10 mg/kg/day orally. Multiple treatments of chlorpyrifos, terbufos, dichlorvos and dimethoate caused death after varying periods of increasing debility; although birds had difficulty walking, they did not display typical symptoms of OPIDN. Fenthion and isofenphos induced drastic weight loss in hens at low levels of treatment; Isofenphos treated hens developed OPIDN, but died soon afterwards. Dichlorvos given at greater than 6 mg/kg/day po or dermally at 1 mg/kg/day produced cholinergic symptoms and most hens died before the end of the treatment period. At lower levels, dichlorvos did not induce overt ataxia. None of the other compounds in this series induced consistent ataxia whether administered orally or dermally. Ethoprop, with an acute oral LD50 near 5 mg/kg and an acute dermal LD50 of approximately 3 mg/kg, was the most toxic compound tested and could not be fully evaluated for its potential to cause OPIDN.

Administration, Oral↗
PubMed1980

Bioconcentration of organophosphorus pesticides to hazardous levels by amphibians.

Organophosphorus pesticides have generally low persistence in the environment, but they may persist in water and accumulate in certain aquatic vertebrates. Frogs are resistant to cholinesterase inhibitors; thus it was suspected that they might accumulate the pesticides. Tadpoles concentrated pesticides from water up to 60 times; those exposed to 1 ppm parathion and 5 ppm fenthion were lethal when they were fed to mallard ducks. Dicrotophos, malathion, and acephate were not accumulated to levels such that they were lethal when consumed in a single meal by ducks. Brain cholinesterase levels were correlated with dose and effect. Metabolites of parathion and fenthion produced by the tadpoles were rapidly excreted and it was concluded that they play a small role in the toxicity of the larvae to ducks. Dangerous levels of some pesticides may be accumulated by amphibians in nature and may adversely affect carnivorous species.

Animals↗
PubMed2006

Vapor phase toxicity of plant essential oils to Cadra cautella (Lepidoptera: Pyralidae).

The toxicities of 44 plant essential oils against larvae of Cadra cautella (Walker) were examined using direct contact and vapor phase toxicity bioassays and compared with the lethal activity of chlorpyrifos-methyl, diazinon, dichlorvos, and fenthion, four widely used organophosphorus insecticides. Responses varied according to plant material used and exposure dose and time. In a filter paper contact toxicity bioassay, potent toxicity was produced from buchu leaf, niaouli, and rosemary oils at 2.4 mg/cm2 and armoise, cypress, galbanum, and mace oils at 4.7 mg/cm2. In vapor phase toxicity bioassays with larvae, cypress, galbanum, niaouli, and rosemary oils were much more effective in closed containers than in open containers, indicating that the lethal effects of these oils were largely because of action in the vapor phase. As judged by 24-h LC50 values, potent fumigant action was observed with niaouli oil (64.7 mg/liter air) and rosemary oil (64.6 mg liter/air). Cypress and galbanum oils exhibited weak fumigant activity. These essential oils were less active than dichlorvos (0.86 mg/liter air). Little or no fumigant action was observed with chlorpyrifos-methyl, diazinon, and fenthion. Essential oils described herein, particularly niaouli and rosemary oils, merit further study as potential larvicides for the control of C. cautella.

Animals↗