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dc.creatorVenceslau, Adneia de Fátima Abreu-
dc.creatorSantos, Fabio Eduardo dos-
dc.creatorSilva, Aline de Fátima-
dc.creatorRocha, Denise Alvarenga-
dc.creatorAbreu, Ademir José de-
dc.creatorJaime, Carlos-
dc.creatorAndrade-Vieira, Larissa Fonseca-
dc.creatorPinto, Luciana de Matos Alves-
dc.date.accessioned2018-07-27T12:14:18Z-
dc.date.available2018-07-27T12:14:18Z-
dc.date.issued2018-04-
dc.identifier.citationVENCESLAU, A. de F. A. et al. Cyclodextrins as effective tools to reduce the toxicity of atrazine. Energy, Ecology and Environment, [S. l.], v. 3, n. 2, p. 81-86, Apr. 2018.pt_BR
dc.identifier.urihttps://link.springer.com/article/10.1007/s40974-017-0073-8pt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/29791-
dc.description.abstractAtrazine (ATZ) is an agrochemical that is still widely used in the Americas to control intrusive weeds in large monocultures. However, its intrinsic toxicity can cause diseases of the endocrine and nervous systems. Cyclodextrins (CDs) are molecular carriers that can be employed to reduce the toxicity of ATZ. In this work, CDs (α, β, and γ) were anchored on silica, forming a hybrid material (CDSI). Lettuce (Lactuca sativa) was used as a model organism to evaluate the toxicity of the following treatments: ATZ; ATZ/α-CD; ATZ/β-CD; ATZ/γ-CD; ATZ/α-CDSI; ATZ/β-CDSI; and ATZ/γ-CDSI. The greatest chromosomal aberrations (CA) and nuclear abnormalities (NA) in the lettuce were observed with non-complexed ATZ. Reductions of CA ranged from 21% for ATZ/α-CD to 59% for ATZ/γ-CDSI, compared to non-complexed ATZ. In the case of NA, the decreases ranged from 29% for ATZ/β-CDSI to 68% for ATZ/α-CD, compared to non-complexed ATZ. The new synthesized CDSI material was found to be a viable option for reducing the toxicity of atrazine herbicide.pt_BR
dc.languageen_USpt_BR
dc.publisherSpringerpt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceEnergy, Ecology and Environmentpt_BR
dc.subjectAtrazine herbicidept_BR
dc.subjectCyclodextrinspt_BR
dc.subjectCytotoxicitypt_BR
dc.subjectHerbicida de atrazinapt_BR
dc.subjectCiclodextrinaspt_BR
dc.subjectCitotoxicidadept_BR
dc.titleCyclodextrins as effective tools to reduce the toxicity of atrazinept_BR
dc.typeArtigopt_BR
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