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Temephos (,,','-tetramethyl ,'-thiodi--phenylene bis(phosphorothioate)) is a larvicide belonging to the family of organophosphate pesticides used for the control of different vectors of diseases, such as dengue, Zika, chikungunya, and dracunculiasis. The aim of this review was to discuss the available published information about temephos toxicokinetics and toxicity in mammals. Temephos is quickly absorbed in the gastrointestinal tract, distributed to all organs, and then it accumulates mainly in adipose tissue. It is metabolized by -oxidation, oxidative desulfuration, and hydrolysis reactions, with the possible participation of cytochrome P450 (CYP). Temephos is mainly eliminated by feces, whereas some of its metabolites are eliminated by urine. The World Health Organization classifies it as class III: slightly dangerous with a NOAEL (no-observed adverse effect level) of 2.3 mg/kg/day for up to 90 days in rats, based on brain acetylcholinesterase (AChE) inhibition. A LOAEL (lowest observable adverse effect level) of 100 mg/kg/day for up to 44 days in rats was proposed based on cholinergic symptoms. However, some studies have shown that temephos causes toxic effects in mammals. The inhibition of the enzyme acetylcholinesterase (AChE) is one of its main demonstrated effects; however, this larvicide has also shown genotoxic effects and some adverse effects on male reproduction and fertility, as well as liver damage, even at low doses. We performed an extensive review through several databases of the literature about temephos toxicokinetics, and we recommend to revisit current assessment of temephos with the new available data.
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http://dx.doi.org/10.1080/10408444.2022.2065967 | DOI Listing |
Am J Trop Med Hyg
August 2025
ICMR-National Institute of Malaria Research Field Unit, Chennai, India.
This study aimed to evaluate the susceptibility of immature Anopheles stephensi to temephos formulation, a primary antilarval intervention currently in operational use. The assessment was conducted against both the WHO-recommended discriminatory dosage with temephos (0.25 parts per million [ppm]) and the operational field dosage with temephos 50% emulsifiable concentrate (EC; 1 ppm).
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
August 2025
Laboratory of Applied Organic Chemistry, Faculty of Sciences and Techniques of Fez, Sidi Mohamed Ben Abdellah University, Fez, Morocco.
The growing need for sustainable mosquito control solutions led us to develop an optimized larvicidal formulation against Culex pipiens Linnaeus, 1758 (Diptera: Culicidae), a key disease vector. Based on preliminary LC evaluations, we developed a synergistic essential oil (EO) blend composed of Artemisia absinthium Linnaeus (58%), A. arborescens L.
View Article and Find Full Text PDFInsects
July 2025
Office of Administrative Interdisciplinary Program on Agricultural Technology, School of Agricultural Technology, King Mongkut's Institute of Technology Ladkrabang, Ladkrabang, Bangkok 10520, Thailand.
The present study evaluated the larvicidal and pupicidal activities of pure and mixed monoterpene formulations-eucalyptol, geranial, -anethole, and -cinnamaldehyde-against and compared them with 1% (/) temephos. Safety bioassays of all formulations on non-target species confirmed their safety. The combined mixture of eucalyptol + -anethole at 400 µg/mL exhibited stronger larvicidal activity, with an LC of 176 µg/mL, while the combination of -anethole + geranial at 400 µg/mL exhibited stronger pupicidal activity with an LC of 167 µg/mL.
View Article and Find Full Text PDFJ Med Entomol
July 2025
Insect Biochemistry and Molecular Biology Laboratory, Department of Zoology, University of North Bengal, Darjeeling, West Bengal, India.
Dengue cases are increasing every year in the sub-Himalayan part of West Bengal, where Aedes albopictus (Skuse 1894) has emerged as a predominant dengue vector. Dengue management heavily relies on the recurrent application of chemical insecticides such as temephos (larvicide) and deltamethrin (adulticide). However Ae.
View Article and Find Full Text PDFJ Biomol Struct Dyn
July 2025
Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research Raebareli (NIPER-R), Lucknow, UP, India.
A series of novel dichloroindolizine carboxylate analogues () have been prepared by using 3,5-dichloropyridine, and substituted phenacyl bromide with electron-deficient acetylene a [3 + 2] cycloaddition reaction. This methodology features a reaction that is free from transition metal or catalyst, providing an eco-friendly synthesis for developing dichloroindolizines. All the synthesized products () were characterized by H NMR,C NMR, and HRMS spectroscopic techniques.
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