Archivos Latinoamericanos de Nutrición (Dec 2007)

Residuos de plaguicidas organoclorados en 4 tipos de aceites vegetales Organochlorine pesticide residues in 4 types of vegetable oils.

  • María Piñero González,
  • Pedro Izquierdo Córser,
  • María Allara Cagnasso,
  • Aiza García Urdaneta

Journal volume & issue
Vol. 57, no. 4
pp. 397 – 401

Abstract

Read online

Esta investigación tuvo como objetivos identificar y cuantificar residuos de los plaguicidas organoclorados (POC) hexaclorobenceno (HCB), lindano, cis-clordano, heptacloro, aldrín, dieldrín, endrín y o,p’-diclorodifeniltricloroetano (o,p’-DDT) en aceites de maíz, soya, girasol y mezclas de aceites, que se expenden en la ciudad de Maracaibo, Venezuela. Se analizaron 30 muestras de 4 tipos de aceites de 10 marcas comerciales. La extracción de residuos de POC se realizó según la técnica de la AOAC. Para la identificación y cuantificación se utilizó un cromatógrafo de gases con detector de captura electrónica (GC-ECD), y para la confirmación, un cromatógrafo de gases acoplado a un espectrómetro de masas (GCMS). Todos los residuos de POC investigados fueron detectados en las muestras analizadas. Se detectaron en mayor concentración (mg/ g) aldrín (0,0088), lindano (0,0054) y o,p’-DDT (0,0035). El análisis estadístico demostró diferencias significativas (PThe present study had as objectives to identify and to quantify organochlorine pesticide residues (OCP) hexachlorobenzene (HCB), lindane, cis-chlordane, heptachlor, aldrín, dieldrín, endrín and o,p’-DDT in vegetable oils of corn, soybean, sunflower and mixtures of oils, sold in the city of Maracaibo, Venezuela. 30 samples of 4 types of vegetable oils of 10 commercial brands were analyzed. The extraction of OCP residues was done according to the Official Method of AOAC. A gas chromatograph with an electronic capture detector (GC-ECD) was used for identification and quantification of OCP residues and confirmation was done with a gas chromatograph coupled with a mass spectrometer (GC-MS). All the OCP residues investigated were detected in the analyzed samples. Aldrin (0.0088), lindane (0.0054) and o,p’-DDT (0.0035) were the OCP residues detected in higher concentrations (mg/g). The statistical analysis showed significant differences (P<0.05) for the concentration of OCP in the different types and commercial brands of vegetable oils. Lindane concentration in the corn oil (0.0125 mg/g), as well as cischlordane (0.0091mg/g) and aldrín (0.0287 mg/g) in the soybean oil exceeded maximal residual limits (MRL) established by Food and Agriculture Organization of the United Nations/World Health Organization (FAO/WHO). In conclusion, it was detected a high incidence of OCP residues in vegetable oils analyzed.

Keywords