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使用气相色谱法分析烘焙食品中脂肪酸和反式脂肪酸的两种衍生化方法的比较

Comparison of two derivatization methods for the analysis of fatty acids and trans fatty acids in bakery products using gas chromatography.

作者信息

Salimon Jumat, Omar Talal A, Salih Nadia

机构信息

School of Chemical Sciences & Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor, Malaysia.

出版信息

ScientificWorldJournal. 2014 Feb 25;2014:906407. doi: 10.1155/2014/906407. eCollection 2014.

DOI:10.1155/2014/906407
PMID:24719581
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3956638/
Abstract

Two different procedures for the methylation of fatty acids (FAs) and trans fatty acids (TFAs) in food fats were compared using gas chromatography (GC-FID). The base-catalyzed followed by an acid-catalyzed method (KOCH3/HCl) and the base-catalyzed followed by (trimethylsilyl)diazomethane (TMS-DM) method were used to prepare FA methyl esters (FAMEs) from lipids extracted from food products. In general, both methods were suitable for the determination of cis/trans FAs. The correlation coefficients (r) between the methods were relatively small (ranging from 0.86 to 0.99) and had a high level of agreement for the most abundant FAs. The significant differences (P = 0.05) can be observed for unsaturated FAs (UFAs), specifically for TFAs. The results from the KOCH3/HCl method showed the lowest recovery values (%R) and higher variation (from 84% to 112%), especially for UFAs. The TMS-DM method had higher R values, less variation (from 90% to 106%), and more balance between variation and %RSD values in intraday and interday measurements (less than 4% and 6%, resp.) than the KOCH3/HCl method, except for C12:0, C14:0, and C18:0. Nevertheless, the KOCH3/HCl method required shorter time and was less expensive than the TMS-DM method which is more convenient for an accurate and thorough analysis of rich cis/trans UFA samples.

摘要

使用气相色谱法(GC-FID)比较了食品脂肪中脂肪酸(FAs)和反式脂肪酸(TFAs)甲基化的两种不同方法。采用碱催化后接酸催化法(KOCH3/HCl)和碱催化后接(三甲基硅基)重氮甲烷(TMS-DM)法,从食品中提取的脂质制备脂肪酸甲酯(FAMEs)。总体而言,两种方法都适用于顺式/反式脂肪酸的测定。两种方法之间的相关系数(r)相对较小(范围为0.86至0.99),对于含量最丰富的脂肪酸具有较高的一致性。对于不饱和脂肪酸(UFAs),特别是反式脂肪酸,可以观察到显著差异(P = 0.05)。KOCH3/HCl法的结果显示回收率值(%R)最低且变化较大(从84%至112%),尤其是对于不饱和脂肪酸。除了C12:0、C14:0和C18:0外,TMS-DM法的回收率值更高,变化更小(从90%至106%),并且在日内和日间测量中变化与%RSD值之间的平衡更好(分别小于4%和6%)。然而,KOCH3/HCl法所需时间较短且成本低于TMS-DM法,对于富含顺式/反式不饱和脂肪酸的样品进行准确和全面的分析,TMS-DM法更方便。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b14a/3956638/bf24031145ca/TSWJ2014-906407.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b14a/3956638/bac89408d3b1/TSWJ2014-906407.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b14a/3956638/9fa5a8ce6e39/TSWJ2014-906407.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b14a/3956638/7f2d0af63c46/TSWJ2014-906407.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b14a/3956638/bf24031145ca/TSWJ2014-906407.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b14a/3956638/bac89408d3b1/TSWJ2014-906407.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b14a/3956638/9fa5a8ce6e39/TSWJ2014-906407.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b14a/3956638/7f2d0af63c46/TSWJ2014-906407.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b14a/3956638/bf24031145ca/TSWJ2014-906407.004.jpg

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