2017
DOI: 10.1016/j.jchromb.2017.07.054
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Characterization of the metabolic transformation of thiamethoxam to clothianidin in Helicoverpa armigera larvae by SPE combined UPLC–MS/MS and its relationship with the toxicity of thiamethoxam to Helicoverpa armigera larvae

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Cited by 20 publications
(12 citation statements)
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“…Approximately 378 commercial formulations of thiamethoxam are registered in China. Clothianidin, (E)-1-(2-chloro-1,3-thiazol-5-ylmethyl)-3-methyl-2-nitroguanidine) is also a neonicotinoid insecticide and a major metabolite of thiamethoxam with similar structure and insecticidal activity [ 5 , 6 ]. In spite of their merits to increase production, the existence of thiamethoxam and clothianidin could cause neurobehavioral alterations in mammals, posing a risk to consumers’ health [ 7 , 8 ].…”
Section: Introductionmentioning
confidence: 99%
“…Approximately 378 commercial formulations of thiamethoxam are registered in China. Clothianidin, (E)-1-(2-chloro-1,3-thiazol-5-ylmethyl)-3-methyl-2-nitroguanidine) is also a neonicotinoid insecticide and a major metabolite of thiamethoxam with similar structure and insecticidal activity [ 5 , 6 ]. In spite of their merits to increase production, the existence of thiamethoxam and clothianidin could cause neurobehavioral alterations in mammals, posing a risk to consumers’ health [ 7 , 8 ].…”
Section: Introductionmentioning
confidence: 99%
“…Liquid chromatography (LC) (Abd-Alrahman, 2014;Jyot and Singh, 2017;Ramasubramanian et al, 2012;Zhou et al, 2006) and LC-MS (Rahman et al, 2015;Valverde et al, 2016) have been widely used to determine residue and dissipation of thiamethoxam (Gupta et al, 2008;Karmakar and Kulshrestha, 2009;Li et al, 2007;Liu et al, 2009;Pareja et al, 2012;Singh and Kulshrestha, 2005). Efforts have also focused on understanding the degradation of thiamethoxam as well as its metabolites (Fan and Shi, 2017;Hilton et al, 2016;Yang et al, 2014). Besides, based on field trials, the dietary risk has been evaluated e.g.…”
Section: Introductionmentioning
confidence: 99%
“…The previous report indicated that thiamethoxam labelled either in the 2-position of the thiazole moiety or on the carbon of the guanidine moiety (4-oxadiazine label) was used in the metabolism and environmental fate studies 5 . Thiamethoxam is transformed to clothianidin in soils, insects and plants, so the part of the insecticidal activity of thiamethoxam was also associated with its metabolite clothianidin 6 . However, the results showed that thiamethoxam and clothianidin would cause rats to release more dopamine in vivo striatum and it seems to be dose-dependent 7 .…”
Section: Introductionmentioning
confidence: 99%