In Situ Preparation of Fatty Acid Methyl Esters for Analysis of Fatty Acid Composition in Foods

1994 ◽  
Vol 59 (6) ◽  
pp. 1262-1266 ◽  
Author(s):  
P.W PARK ◽  
R.E. GOINS
Author(s):  
N. A. Zhizhin

The paper presents one of the approaches for identifying fatty acids using gas chromatography, which significantly reduces the analysis time, and is equally effective when compared with the traditional method of studying the fatty acid composition. The determination of the composition of fatty acids today is a guarantee of quality in identifying various conformations and modifications of milk fat, the bioactive properties of individual acids of the omega-3 and omega-6 families, etc. Moreover, this method is time-consuming, therefore, the goal of this work is to optimize the parameters of this methodology for quick and regular analysis of fatty acid composition in laboratories and dairy enterprises. The analysis of the fatty acid composition was carried out using two columns with different stationary phases. A comparative evaluation of the analytical characteristics was carried out on two capillary chromatographic columns: SP-2560 100 ? 0.25 mm ID, 0.2 ?m with a stationary phase FFAP (traditional) and a gas chromatographic column BPX-70: stationary phase 70% cyanopropylphenyl dimethylpolysiloxane, 10 m ? 0.1 m ? 0.20 ?m. Detection was carried out using a flame ionization detector. A mixture of Supelco® 37 FAME Mix fatty acid methyl esters and Sigma-Aldrich methyl decanoate analytical standard was used as the standard. For data processing, the NetChrom software was used, the composition of fatty acid methyl esters was calculated by the internal normalization method. The analysis time of the first column was 49.07 minutes, for the second 8.44, respectively. The use of a stationary phase column of cyanopropylphenyl dimethylpolysiloxane significantly reduced the analysis time when eluting a complex composition of fatty acids. The studies were carried out using modern analytical techniques and arbitration methods of analysis in the laboratory of technochemical control of the All-Russian Scientific Research Institute of the Dairy Industry. This adapted analysis method will be of interest to specialists in the field of laboratory research and processing enterprises.


2019 ◽  
Vol 248 ◽  
pp. 526-537 ◽  
Author(s):  
Charles Felix ◽  
Aristotle Ubando ◽  
Cynthia Madrazo ◽  
Ivan Henderson Gue ◽  
Sylviana Sutanto ◽  
...  

2000 ◽  
Vol 55 (7-8) ◽  
pp. 569-575 ◽  
Author(s):  
Debra L. Bemis ◽  
Vassilios Roussis ◽  
Constantinios Vagias ◽  
Robert S. Jacobs

Abstract Chloroplasts isolated from three populations of the tropical marine Chlorophyte Anadyomene stellata collected off the coast of Greece were analyzed for their fatty acid composition. Following the preparation of fatty acid methyl esters, GC-MS (El) was utilized to identify the fatty acids present in each population. Including isomers, the fatty acid profile of all three algal populations was comprised of 19 fatty acids (4 saturated, 6 monounsaturated, 9 polyunsaturated) with palmitic acid present in the highest amounts (25-27% of total fatty acids). Analysis of variance revealed significant differences amongst the three populations in the percent of total fatty acids for twelve of the fatty acids. High levels of C20 PUFAs, an atypical observation in Chlorophytes, were observed in all three populations comprising approximately 17% of total fatty acids. Furthermore a 14:2 PUFA , apparently rare in marine macrophytic Chlorophytes, was identified in significant quantities. Surprisingly, we did not find any of the conjugated tetraene containing fatty acids that we previously identified in the A. stellata populations studied from the Florida Keys.


1996 ◽  
Vol 51 (3-4) ◽  
pp. 151-154 ◽  
Author(s):  
Eugène Ucciani ◽  
Alain Debal ◽  
Michel Gruber ◽  
Robert L. Wolff

Abstract The fatty acid composition of seed oils of eight Ranunculaceae was determinated in order to characterize new sources of gamma-linolenic acid. Fatty acids were identified as fatty acid methyl esters (FAME) by capillary gas-liquid chromatography (GC) and capillary GC-Fourier transform infrared spectroscopy (FTIR). For trienic FAME the use of a cyanopropyl-polysiloxane stationary phase (CP-Sil 88) allowed the separation with high resolution of methyl ester of columbinic acid (trans-5,cis-9,cis-12 18:3) and gamma-linolenic acid (cis-6,cis-9,cis-12 18:3). The results confirmed the presence of columbinic acid in Thalictrum seed oils, and that of gamma-linolenic acid in Anemone and related species seed oils. The taxonomic subdivision of Ranunculaceae into sub-families and tribes, which resulted from morphological considerations, did not account for the above results.


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