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1.
Talanta ; 273: 125870, 2024 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-38460423

RESUMO

Pyroxasulfone is a selective, systemic, pre-emergence herbicide which acts to inhibit weeds in potato, coffee, sugar cane, eucalyptus, and soybean plantations, among others. This active ingredient was classified by Brazilian legislation as a very dangerous product for the environment, and to date there are no studies involving the development of extraction methods for monitoring this compound in environmental matrices. Therefore, the objective of this study was to optimize and validate liquid-liquid extraction with low temperature purification followed by a gas chromatography coupled to mass spectrometry analysis to determine this herbicide in honey samples. The results showed that the best extractor phase was acetonitrile and ethyl acetate (6.5 mL:1.5 mL), with recovery rates close to 100% and relative standard deviations below 11%. The validation proved that the extraction method was selective, precise, accurate and linear in the range of 3-225 µg kg-1, reaching a limit of quantification of 3 µg kg-1, with a -25.95% matrix effect. Monitoring on real samples did not reveal episodes of environmental contamination with pyroxasulfone residue.


Assuntos
Herbicidas , Mel , Isoxazóis , Sulfonas , Herbicidas/análise , Cromatografia Gasosa-Espectrometria de Massas/métodos , Temperatura , Mel/análise , Extração Líquido-Líquido , Cromatografia Líquida de Alta Pressão , Extração em Fase Sólida
2.
Anal Methods ; 14(30): 2945-2952, 2022 08 04.
Artigo em Inglês | MEDLINE | ID: mdl-35861165

RESUMO

Fluopyram is a fungicide and nematicide that belongs to the chemical group of benzamides, which act as succinate dehydrogenase inhibitors (SDHIs) on the mitochondrial respiratory chain of fungi. Despite being well known in several countries, there are few studies involving the optimization and validation of extraction methods for determining fluopyram in water samples. Therefore, this study aimed to optimize and validate liquid-liquid extraction with low-temperature purification (LLE-LTP) to determine fluopyram fungicide in water samples using high-performance liquid chromatography with diode array detection (HPLC-DAD). A two-level full factorial design was employed to optimize LLE-LTP which enabled achieving a recovery rate close to 100% and relative standard deviations (RSD) < 10.0%. The validation showed that the extraction method may be considered selective, precise, accurate, and linear in the range of 6.0 to 200 µg L-1. The LOD and LOQ were 4.0 and 6.0 µg L-1, respectively, proving the efficiency of this method for trace level determination of this fungicide in water samples. LLE-LTP coupled to HLPC-DAD analysis showed a matrix effect of less than 8% and it was applied in monitoring 20 environmental water samples, but no fluopyram residue was detected in the samples.


Assuntos
Fungicidas Industriais , Benzamidas/análise , Cromatografia Líquida de Alta Pressão/métodos , Fungicidas Industriais/análise , Extração Líquido-Líquido/métodos , Temperatura , Água/análise
3.
Anal Methods ; 13(16): 1955-1964, 2021 04 28.
Artigo em Inglês | MEDLINE | ID: mdl-33913942

RESUMO

Honey is widely consumed worldwide, however, this food can be contaminated by chemical contaminants, such as the insecticide dichlorodiphenyltrichloroethane (DDT). Despite legal restrictions on DDT use, this organochlorine pesticide has been detected in honey collected in several developed and developing countries, representing risks to human health, animals, and the environment due to its high environmental persistence, potential carcinogenicity, and ecotoxicological effects. Thus, the development of an analytical method for DDT monitoring in this matrix is important to ensure food security. Therefore, this study aimed to optimize and validate a simple, low-cost, and efficient method using the liquid-liquid extraction with low-temperature purification (LLE-LTP) to determine DDT in honey samples by high-performance liquid chromatography with diode array detector (HPLC-DAD). The proposed method was validated according to SANTE guidelines, being considered selective, precise, accurate, and linear in the range of 8.0-160 µg kg-1. The limits of detection (LOD) and quantification (LOQ) achieved were 4.0 and 8.0 µg kg-1, respectively. This LOQ value is lower than the maximum residue limit established by the Brazilian and European Union legislation. Therefore, the LLE-LTP combined to HPLC-DAD allows the routine analysis of DDT in honey samples and can be widely applied in studies to monitor this pesticide, especially in developing countries, where DDT use is still allowed.


Assuntos
Mel , Animais , Brasil , Cromatografia Líquida de Alta Pressão , DDT/análise , Mel/análise , Humanos , Extração Líquido-Líquido , Temperatura
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