About: Imiprothrin is a research topic. Over the lifetime, 6 publications have been published within this topic receiving 116 citations. The topic is also known as: Imiprothrin.
TL;DR: A new rapid and sensitive electron ionization gas chromatography-mass spectrometry method in selective ion monitoring mode (SIM) was developed for the determination of l3 synthetic pyrethroid insecticide molecules and their stereo isomers in whole blood.
TL;DR: It is indicated that repeated noncontinuous inhalation of a commonly utilized insecticide that contains imiprothrin and deltamethrin can cause a variety of immunotoxic effects in sites distal to the lungs.
Abstract: A commonly available aerosolized pyrethroid insecticide containing deltamethrin and imiprothrin is widely used for hygienic control in Egypt. The immunotoxic effects after inhalation exposures to the preparation of each for 2, 10, and 30 days were investigated in rats. For each exposure, the insecticide (containing 0.2% imiprothrin and 2.5% deltamethrin) was sprayed in all directions in a room (using a special attachment located in the ceiling in the center of the room) for 30 s each minute for 15 min; the room was then kept closed for 15 min. After each spray interval, the rats were introduced for 30 min and then removed to a clean room. The exposure process was repeated a total of three times on each day of the respective regimens. The interval between the 15-min spray/15-min pause/30-min rat exposure cycles was 120 min. Twenty-four hours after the final exposure in each particular regimen, the cohort rats in the regimen (air and exposed) were weighed, sacrificed, and their tissues were removed for analyses. Immunological tests performed included assessments of potential changes in immunopathology (determined from body and splenic weights), humoral-mediated immunity (based on plaque-forming activity of spleen cells), cell-mediated immunity (determined from splenic lymphocyte responsiveness to stimulation with phytohemagglutinin and immune cell (sub)type profile analyses), and nonspecific immunity (based on phagocytic activity of peritoneal macrophages). The results indicated that of all the endpoints examined, among the rats exposed over a 2-day period to the imiprothrin- and deltamethrin-containing insecticide aerosol, the only significant change noted (relative to values from time-matched controls) was in the levels of splenic CD4+CD8- and CD4+ CD8+ cells. In contrast, exposures on each day of a 10-day period led to significant decreases in several endpoints; exceptions to this were values for body and spleen weight (unaffected), splenic OX12-OX19+ levels (significant increase), and CD4+CD8- levels (unaffected, relative to control). Rats exposed for 30 days displayed significant decreases in each test applied, except for increases in both splenic OX12-OX19+ and CD4+CD8- cell levels relative to corresponding control rat values. The present study findings indicate that repeated noncontinuous inhalation of a commonly utilized insecticide that contains imiprothrin and deltamethrin can cause a variety of immunotoxic effects in sites distal to the lungs.
TL;DR: The proposed method was successfully applied for the determination of pyrethroids in mosquito coils and two aerosol products and the recovery of transallethrin in mosquito coil at three spiked levels was 96.8% with relative standard deviation less than 2.7%.
TL;DR: In this article, a unique type of pyrethroid having an imidazolidinyl ring in its alcohol moiety, was rapidly degraded in two aerobic U.S. soils.
Abstract: Imiprothrin, a unique type of pyrethroid having an imidazolidinyl ring in its alcohol moiety, was rapidly degraded in two aerobic U.S. soils. The half-lives of biologically active trans isomer were estimated by assuming the first-order kinetics to be 1.6–2.5 days, shorter than those of the cis isomer (3.3–12.5 days). The primary metabolic pathway was ester cleavage followed by instantaneous elimination of a hydroxylmethyl group from the alcohol moiety to form PGH (1-propargylimidazolidine-2,4-dione). The opening of the imidazolidinyl ring with subsequent release of the carbamoyl group resulted in the formation of PG (N-propargylglycine). The soil adsorption coefficients (Koc) of the trans isomer, the main component of imiprothrin (80%), to the two soils were determined to be 376 and 428 (ml/g o.c.) by the batch equilibrium method and these lower values as compared with other pyrethroids were likely to stem from the hydrophilic character of the alcohol moiety. Based on the metabolic half-lives and Koc values, the groundwater concentration of imiprothrin was calculated to be 0.039 μg/L by using the screening simulation model SCI-GROW known to give a conservative groundwater concentration. This significant lower concentration clearly indicates that imiprothrin is most unlikely to contaminate the groundwater, mainly due to its rapid degradation in soil.
TL;DR: In this article, the problem of providing a direct-hit type aerosol having an excellent control effect against insect pests is addressed, provided that the pyrethroid compound is one represented by the formula (I), and even more preferably one compound selected from the group consisting of imiprothrin, tetramethrin, prallethrin, transfluthrin, metofluthrin and dime fluthrin.
Abstract: PROBLEM TO BE SOLVED: To provide a direct hit type aerosol having an excellent control effect against insect pestsSOLUTION: Provided is a direct hit type aerosol comprising at least one pyrethroid compound, an organic solvent, and a propellant, wherein a value (β) calculated according to the following formula is in a range of 05 to 25 Preferably, the pyrethroid compound is one represented by the formula (I), and even more preferably at least one compound selected from the group consisting of imiprothrin, tetramethrin, prallethrin, transfluthrin, metofluthrin, dimefluthrin, 2,3,5,6-tetrafluoro-4-methylbenzyl 2,2-dimethyl-3-(1-propenyl) cyclopropanecarboxylate, and the like Formula) β=(spray arrival distance) (cm)×(spray quantity (g) per 1 second)÷(weight concentration (%) of pyrethroid compound)