کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1241700 1495775 2016 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A preconcentration method for indirect determination of acrylamide from chips, crackers and cereal-based baby foods using flame atomic absorption spectrometry
ترجمه فارسی عنوان
یک روش پیشکنترل برای تعیین غیر مستقیم آکریل آمید از تراشه ها، کراکر ها و غذاهای کودک مبتنی بر غلات با استفاده از طیف سنج جذب اتمی شعله
کلمات کلیدی
آکریلامید، غذاهای کودک، فلورسین، ایمنی مواد غذایی، پیش انقباض
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• A preconcentration method is developed for indirect detection of acrylamide in foods by FAAS.
• Ion-pairing, fluorescein in presence of Ni(II) at pH 9.0 is employed for sensitivity improvement.
• The method provides a low detection limit enough to meet the food safety requirements.
• The method is validated through the analysis of two CRMs.
• The method is successfully applied to indirect detection of acrylamide in selected foodstuffs.

Acrylamide is a toxic species for human health, and is a Maillard reaction product which forms spontaneously in heat treatment process of foods. Therefore, a simple, fast and cost-effective method was developed for the indirect determination of acrylamide in processed foods particularly consumed by children. The method is based on ion–pairing of acrylamide with fluorescein (F2−) in presence of Ni(II) ions at pH 9.0, and then extraction of the formed ternary complex into micellar phase of poly(ethyleneglycol-mono-p-nonylphenylether) (PONPE 7.5) before analysis by flame atomic absorption spectrometry (FAAS). The ultrasonic-assisted cloud point extraction (UA-CPE) has been used for the preconcentration of acrylamide in the samples prior to its FAAS detection. The matrix matched calibration curve is linear in range of 0.3–150 µg kg−1 under optimal reagent conditions (1.75 mL of 0.1 mol L−1 ammonia buffer at pH 9.0, 2.2 mg L−1 Ni(II), 4.0×10−4 mol L−1 F2−, 0.4% (w/v) NH4Cl and 0.7% (v/v) PONPE 7.5) with sensitivity enhancement of 160-fold. The proposed method has been validated by assessment of the following parameters; the limits of detection (LOD) and quantification (LOQ) (0.08 µg kg−1 and 0.28 µg kg−1, respectively) with a relative standard deviation (RSD%) lower than 6.3%, and extractive recovery higher than 95% for acrylamide spiked at levels of 5 and 25 µg kg−1. The method was successfully applied to the indirect determination of acrylamide in the processed foods and two CRMs with satisfactory results.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Talanta - Volume 161, 1 December 2016, Pages 143–150
نویسندگان
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