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Title: | Single-laboratory validation of a saponification method for the determination of four polycyclic aromatic hydrocarbons in edible oils by HPLC-fluorescence detection | Authors: | Akdoğan, Abdullah Buttinger, G. Wenzl, T. |
Keywords: | Edible oil extraction high-performance liquid chromatography polycyclic aromatic hydrocarbons saponification Aromatic compounds Aromatic hydrocarbons Aromatization Chromatography Extraction High performance liquid chromatography Hydrocarbons Hydrolysis Liquid chromatography Liquids Oils and fats Olive oil Phase separation Pyrene Saponification Sunflower oil Uncertainty analysis Concentration levels HPLC-fluorescence detection Limits of detection Liquid partitioning Method validations Relative measurement Single laboratory validations Solid-phase extraction Polycyclic aromatic hydrocarbons benzo[a]pyrene benzo[b]fluoranthene benz[a]anthracene chrysene corn oil edible oil olive oil polycyclic aromatic hydrocarbon sesame seed oil sunflower oil vegetable oil Article fluorescence high performance liquid chromatography limit of detection limit of quantitation liquid liquid extraction measurement accuracy measurement repeatability priority journal solid phase extraction chemistry laboratory spectrofluorometry validation study Chromatography, High Pressure Liquid Fluorescence Laboratories Plant Oils Polycyclic Aromatic Hydrocarbons Solid Phase Extraction Spectrometry, Fluorescence |
Publisher: | Taylor and Francis Ltd. | Abstract: | An analytical method is reported for the determination of four polycyclic aromatic hydrocarbons (benzo[a]pyrene (BaP), benz[a]anthracene (BaA), benzo[b]fluoranthene (BbF) and chrysene (CHR)) in edible oils (sesame, maize, sunflower and olive oil) by high-performance liquid chromatography. Sample preparation is based on three steps including saponification, liquid–liquid partitioning and, finally, clean-up by solid phase extraction on 2 g of silica. Guidance on single-laboratory validation of the proposed analysis method was taken from the second edition of the Eurachem guide on method validation. The lower level of the working range of the method was determined by the limits of quantification of the individual analytes, and the upper level was equal to 5.0 µg kg-1. The limits of detection and quantification of the four PAHs ranged from 0.06 to 0.12 µg kg-1 and from 0.13 to 0.24 µg kg-1. Recoveries of more than 84.8% were achieved for all four PAHs at two concentration levels (2.5 and 5.0 µg kg-1), and expanded relative measurement uncertainties were below 20%. The performance of the validated method was in all aspects compliant with provisions set in European Union legislation for the performance of analytical methods employed in the official control of food. The applicability of the method to routine samples was evaluated based on a limited number of commercial edible oil samples. © 2016 The Author(s). Published by Taylor & Francis. | URI: | https://hdl.handle.net/11499/9703 https://doi.org/10.1080/19440049.2015.1127430 |
ISSN: | 1944-0049 |
Appears in Collections: | Denizli Teknik Bilimler Meslek Yüksekokulu Koleksiyonu PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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