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采用气扩散微萃取结合分散液相微萃取法测定食用油脂中丙二醛、丙烯醛和其他四种脂质过氧化产物。

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

机构信息

Department of Analytical Chemistry, Nutrition and Food Science, Faculty of Chemistry, University of Santiago de Compostela, 15782, Spain; Health Research Institute of Santiago de Compostela (IDIS), University of Santiago de Compostela, 15782, Spain.

Department of Analytical Chemistry, Nutrition and Food Science, Faculty of Chemistry, University of Santiago de Compostela, 15782, Spain.

出版信息

J Chromatogr A. 2020 Sep 13;1627:461397. doi: 10.1016/j.chroma.2020.461397. Epub 2020 Jul 8.

Abstract

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≥0.9974, in the range from 0.15 or 0.3 µg·g to 3 µg·g. Limits of detection and limits of quantification were 0.05 or 0.10 and 0.15 or 0.3 µg·g, 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 µg·g.

摘要

一种新的、灵敏的用于同时测定次级脂质过氧化醛的分析方法已经成功开发并验证。使用 2,4-二硝基苯肼(DNPH)通过气相扩散微萃取(GDME)与分散液液微萃取(DLLME)结合,对丙二醛、丙烯醛、甲醛、乙醛、丙醛和戊醛进行提取和衍生,然后用于气相色谱-质谱(GC-MS)分析。通过实验设计对实验条件进行了优化。根据美国食品和药物管理局(FDA)的指导意见对分析方法进行验证,结果表明,在 0.15 或 0.3 µg·g 至 3 µg·g 的范围内,线性度良好,r≥0.9974。检出限和定量限分别为 0.05 或 0.10 和 0.15 或 0.3 µg·g。精密度以相对标准偏差(RSD≤9.5%)表示,回收率在 95%至 110%之间。该方法应用于 48 种食用油样品中醛的表征;在果渣橄榄油中发现了最高浓度的丙二醛,为 6.64 µg·g。

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