Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/9703
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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