کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1188476 | 963489 | 2009 | 6 صفحه PDF | دانلود رایگان |

Three non-fatty ready-to-eat baby food matrices (fruits: juice, purée and cocktail plus rice flour/starch and sugar) were fortified with 0.01, 0.05, 0.1 and 0.2 mg/kg of dimethoate, chlorpyrifos, methidathion, phosalone and diazinon. Simple methods including extraction by ethyl acetate [EtAc] and acetone partition and determination by gas chromatography with Nitrogen–Phosphorus Detector (GC–NPD) were used. Acceptable pesticides recoveries (70–110%), low detection and quantification limits (0.001 to >0.1 mg/kg and 0.005 to 0.04 mg/kg, respectively) and repeatabilities (%RSDs), in 0.01 mg/kg, within 2.9–13.9% were observed. However, analytes recoveries were affected (p < 0.05) by both the baby food formulation and the extraction method used. Specifically, fruits purée and cocktail EtAc extracts gave excessively over-(dimethoate recoveries of 119.7–153.5%) or underestimation (phosalone and especially diazinon recoveries of 19.3–79.2%) in contrast to fruits juice (e.g., 61.3–87.9%). Also, EtAc extracts showed higher amount of lipophilic compounds and provided lower recoveries for non-polar analytes than those of acetone partition. Consequently, the examined methods may be successfully applied in non-fatty baby foods with the matrix-matched standards determination, following improvements of certain parameters in relation to the clean-up of samples.
Journal: Food Chemistry - Volume 115, Issue 3, 1 August 2009, Pages 1164–1169