Desenvolvimento e validação de método analítico por dispersão da matriz em fase sólida e cromatografia em fase gasosa acoplada a espectrometria de massas para determinação de pesticidas em amostras de ovos de galinha (Gallus gallus domesticus)

Detalhes bibliográficos
Ano de defesa: 2012
Autor(a) principal: Souza, Michel Rubens dos Reis lattes
Orientador(a): Dórea, Haroldo Silveira lattes
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Sergipe
Programa de Pós-Graduação: Pós-Graduação em Química
Departamento: Não Informado pela instituição
País: BR
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: https://ri.ufs.br/handle/riufs/6044
Resumo: The eggs are of great nutritional value. Its biochemical composition indicates the source of proteins, lipids, vitamins and minerals. However, undesirable chemical compounds can form part of this constitution. The pesticides, when applied irregularly, can represent a serious health risk to consumers if detected above the maximum residue limits, can be identified in egg white and yolk. The objective of this study was to develop and to validate an analytical method for matrix solid phase dispersion and gas chromatography coupled with mass spectrometry for determination of atrazine, pirimicarb, lindane, permethrin, deltamethrin, cypermethrin, ethion, bifenthrin and alachlor in chicken eggs (Gallus gallus domesticus) marketed in the city of Aracaju-SE, Brazil. Among the sorbents were tested: silica, neutral alumina, Florisil® and C18. The various combinations matrix/dispersant/co-column were analyzed. The system: matrix of lyophilized egg (0,25 g)/dispersant Florisil® (1,5 g)/auxiliary column C18 (0,5 g) was more efficient. The acetonitrile (10 mL) was chosen as the eluting solvent. The recoveries (n = 3) ranged from 69,6 a 103,8% with relative standard deviation ranging from 16,2 a 45,5%. The validation of the analytical method was performed through the following parameters: the selectivity, it s showing that the method is selective for all pesticides; the linearity, in terms of linear coefficient of the calibration curve, above 0,99 for all pesticides, for a given concentration range from 0,01 to 2,0 μg g-1; the sensibility, with the pesticide bifenthrin as the more sensitive and less sensitive to cypermethrin; the limits of detection and quantification limits in the intervals of 0,003 to 0,015 μg g-1 and 0,01 to 0,05 μg g-1, respectively; the recovery (n = 3), to levels 0,5, 1,0 and 1,5 μg g-1 ranged from 61,6 to 95%; the accuracy in terms of relative standard deviation (RSD) in the range of 0,13 to 29,92%; and application in real samples that showed in one of samples the pesticide bifenthrin in a concentration of 0,004 μg g-1, below the limit of quantification (<LQ). Therefore the union of technical MSPD-GC/MS provided a quick, easy and efficient extraction for determination of selected pesticides in chicken eggs.