Determination of malondialdehyde, acrolein and four other products of lipid peroxidation in edible oils by Gas-Diffusion Microextraction combined with Dispersive Liquid-Liquid Microextraction

被引:22
作者
Custodio-Mendoza, J. A. [1 ,2 ]
Aja-Macaya, J. [1 ]
Valente, I. M. [3 ,4 ]
Rodrigues, J. A. [3 ]
Almeida, P. J. [3 ]
Lorenzo, R. A. [1 ,2 ]
Carro, A. M. [1 ,2 ]
机构
[1] Univ Santiago de Compostela, Fac Chem, Dept Analyt Chem Nutr & Food Sci, Santiago De Compostela 15782, Spain
[2] Univ Santiago de Compostela, Hlth Res Inst Santiago de Compostela IDIS, Santiago De Compostela 15782, Spain
[3] Univ Porto, REQUIMTE LAQV Dept Quim & Bioquim, Fac Ciencias, P-4169007 Porto, Portugal
[4] Univ Porto, Inst Ciencias Biomed Abel Salazar, Dept Clin Vet, REQUIMTE LAQV ICBAS, Rua JorgeViterbo Ferreira 228, P-4050313 Porto, Portugal
关键词
Aldehydes; acrolein; Dispersive liquid-liquid microextraction; Gas-diffusion microextraction; GC-MS; Lipid oxidation; SOLID-PHASE EXTRACTION; CHROMATOGRAPHY; ALDEHYDES; FOOD; DERIVATIZATION; MEMBRANE; MARKERS; MILK;
D O I
10.1016/j.chroma.2020.461397
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new and sensitive analytical method for the simultaneous determination of secondary lipid peroxidation aldehydes has been successfully developed and validated. Malondialdehyde, acrolein, formaldehyde, acetaldehyde, propanal, and pentanal were extracted and derivatized using 2,4-dinitrophenylhydrazine (DNPH) by gas-diffusion microextraction (GDME) combined with dispersive liquid-liquid microextraction (DLLME) for gas chromatography-mass spectrometry (GC-MS) analysis. The experimental conditions have been optimized by experimental designs. The analytical method validation, in accordance to the Food and Drug Administration (FDA) guidance, provided good results in terms of linearity with r(2) =0.9974, in the range from 0.15 or 0.3 mu g.g(-1) to 3 mu g.g(-1). Limits of detection and limits of quantification were 0.05 or 0.10 and 0.15 or 0.3 mu g.g(-1), respectively. Precision was tested as a relative standard deviation (RSD= 9.5%) and recoveries were between 95% and 110%. The method was applied in the characterization of aldehydes in forty-eight edible oil samples; with the highest concentration found in pomace olive oil for malondialdehyde at 6.64 mu g.g(-1). (c) 2020 Elsevier B.V. All rights reserved.
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页数:9
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