Extraction method for determining dinotefuran insecticide in soil samples

dc.creatorSandro Braga Soares
dc.creatorLázaro Chaves Sicupira
dc.creatorGevany Paulino de Pinho
dc.creatorFlaviano Oliveira Silvério
dc.date.accessioned2025-07-15T11:59:42Z
dc.date.accessioned2025-09-08T23:49:18Z
dc.date.available2025-07-15T11:59:42Z
dc.date.issued2024
dc.description.sponsorshipCNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico
dc.description.sponsorshipFAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas Gerais
dc.identifier.doihttps://doi.org/10.21577/0103-5053.20230190
dc.identifier.issn1678-4790
dc.identifier.urihttps://hdl.handle.net/1843/83564
dc.languageeng
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofJournal of the brazilian chemical society
dc.rightsAcesso Aberto
dc.subjectSolos - Lixiviação
dc.subjectExtração por solventes
dc.subjectInseticidas
dc.subjectPragas agrícolas
dc.subjectCromatografia líquida de alta eficiência
dc.titleExtraction method for determining dinotefuran insecticide in soil samples
dc.typeArtigo de periódico
local.citation.issue6
local.citation.spagee-20230190
local.citation.volume.35
local.description.resumoDinotefuran is a third-generation neonicotinoid insecticide that has a broad action spectrum in agriculture pests. Dinotefuran was authorized in Brazil in 2019, being classified as a very dangerous product for the environment. Therefore, this study aimed to optimize and validate the solid-liquid extraction with low temperature purification to determine dinotefuran in soil samples using high-performance liquid chromatography coupled diode array detection. The results showed that the best extracting phase was acetonitrile:water (8:2 v/v), followed by the clean-up with 50 mg of primary-secondary amine. The method under these conditions has a linear range of 15.0 to 140 µg k g-1 and reached limits of detection and quantification of 10.0 and 15.0 µg kg-1, respectively. The validation revealed that the method was selective, precise, accurate, and presented a matrix effect of 15%. Although dinotefuran was not detected in real soil samples, the proposed method proved to be an efficient alternative for monitoring dinotefuran in soil samples.
local.publisher.countryBrasil
local.publisher.departmentICA - INSTITUTO DE CIÊNCIAS AGRÁRIAS
local.publisher.initialsUFMG
local.url.externahttps://www.scielo.br/j/jbchs/a/pGtkg7SRk9LKtc3gLPqwhxx/?lang=en

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