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Enrichment and quantification of monoacylglycerols and free fatty acids by solid phase extraction and liquid chromatography-mass spectrometry
被引:12
|作者:
Chu, Boon-Seang
[1
,2
]
Nagy, Kornel
[4
,1
]
机构:
[1] Nestec Ltd, Nestle Res Ctr, Food Sci & Technol Dept, CH-1000 Lausanne, Switzerland
[2] Univ Teknol Malaysia, Inst Bioprod Dev, Skudai, Johore, Malaysia
来源:
关键词:
Monoacylglycerol;
Free fatty acid;
Oil;
Animal fat;
Tandem mass spectrometry;
ATMOSPHERIC-PRESSURE PHOTOIONIZATION;
GAS-CHROMATOGRAPHY;
CHEMICAL-IONIZATION;
BIOLOGICAL SAMPLES;
DIRECT SEPARATION;
VEGETABLE-OILS;
METHYL-ESTERS;
RAPID METHOD;
DESORPTION/IONIZATION;
TRIACYLGLYCEROLS;
D O I:
10.1016/j.jchromb.2013.05.026
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Quantification of monoacylglycerols (MAG) and free fatty acids (FA) is of interest in biological systems, in food, cosmetic and pharmaceutical products. This manuscript describes and validates a reversed phase liquid chromatography-tandem mass spectrometry based approach for simultaneous quantification of these analytes in fats and oils. Purification and concentration of MAG/FA were performed using cation exchange solid phase extraction, which allowed elimination of the abundant triacylglycerols. Following cleanup and concentration, the analytes were separated and detected with the aid of volatile ammonium-formate buffer. MAG were detected in positive ion mode, while FA were detected in negative ion mode. The method was validated by the method of standard additions and using stable isotope labeled internal standards. The results confirm the feasibility of quantifying these two classes of analytes simultaneously without any chemical derivatization. The obtained main quantitative features include: (1) lower limits of quantification 1-30 ppm for MAG analytes, (2) lower limits of quantification 90-300 ppm for FA analytes, (3) averaged inter-batch precision 6%, and (4) averaged bias -0.2% for MAG and 0.5% for FA. Various animal fat and vegetable oil samples were characterized for their MAG/FA profile indicating the usefulness of the method to address quality and authenticity of fats and oils. (C) 2013 Elsevier B.V. All rights reserved.
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页码:50 / 58
页数:9
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