Validation of acetate QuEChERS methodology for pesticides multiresidue analysis in soybean samples and soybean-soluble extract by means of high-performance liquid chromatography coupled to tandem mass spectrometry

  • Adherlene Vieira Gouvêa Fundação Oswaldo Cruz, Instituto Nacional de Controle da Qualidade em Saúde, Laboratório de Alimentos e Contaminantes, Rio de Janeiro, RJ
  • Maria Helena Wohlers Morelli Cardoso Fundação Oswaldo Cruz, Instituto Nacional de Controle da Qualidade em Saúde, Laboratório de Alimentos e Contaminantes, Rio de Janeiro, RJ
  • Lucia Helena Pinto Bastos Fundação Oswaldo Cruz, Instituto Nacional de Controle da Qualidade em Saúde, Laboratório de Alimentos e Contaminantes, Rio de Janeiro, RJ
  • Cristiane Barata Silva Fundação Oswaldo Cruz, Instituto Nacional de Controle da Qualidade em Saúde, Laboratório de Alimentos e Contaminantes, Rio de Janeiro, RJ
  • Nina Daddario Ortiz Universidade Federal do Rio de Janeiro, Instituto de Química, Departamento de Bioquímica, Unidade Proteômica, Rio de Janeiro, RJ
  • Armi Wanderley da Nóbrega Fundação Oswaldo Cruz, Instituto Nacional de Controle da Qualidade em Saúde, Laboratório de Alimentos e Contaminantes, Rio de Janeiro, RJ
  • Silvana do Couto Jacob Fundação Oswaldo Cruz, Instituto Nacional de Controle da Qualidade em Saúde, Laboratório de Alimentos e Contaminantes, Rio de Janeiro, RJ
Keywords: soybeans, pesticides, validation studies, chromatography, liquid, mass spectrometry

Abstract

The possibility of occurring the soy and soy derivatives samples contamination with pesticide residues has become significant due to the increased use of these products in human nourishment. In this context, the present study aimed at validating the acetate QuEChERS multiresidue methodology for analyzing 144 pesticide residues in soybean samples and soybean soluble extract using high-performance liquid chromatography coupled to tandem mass spectrometry. The parameters evaluated were: selectivity (matrix effect in the two sample types), linearity (working range, regression significance, homogeneity of the regression residues), accuracy (recovery), precision (repeatability) and limits of detection and quantification. The analytical curves presented R2 ≥ 0.95 and r ≥ 0.98 in the working range (0.002 to 0.200 μg.mL-1). The accuracy and precision evaluated at two levels of fortification of two matrices presented values of recovery in the 70-120 % range and CV (%) ≤ 20 %, respectively. The limits of detection nd quantification showed satisfactory results. The validated methodology allowed to perform the determination of 122 substances in the matrix soybean and 124 in the soluble extract of soybean.
Published
2015-10-01
How to Cite
Gouvêa, A. V., Cardoso, M. H. W. M., Bastos, L. H. P., Silva, C. B., Ortiz, N. D., Nóbrega, A. W. da, & Jacob, S. do C. (2015). Validation of acetate QuEChERS methodology for pesticides multiresidue analysis in soybean samples and soybean-soluble extract by means of high-performance liquid chromatography coupled to tandem mass spectrometry. Revista Do Instituto Adolfo Lutz, 73(1), 40-58. https://doi.org/10.18241/0073-98552014731588
Section
ORIGINAL ARTICLE