Analysis of cyclopropenoid fatty acids by raman spectroscopy

1981 ◽  
Vol 118 (2) ◽  
pp. 364-370 ◽  
Author(s):  
Saima Kint ◽  
Robert E. Lundin ◽  
A.C. Waiss ◽  
Carl A. Elliger
2018 ◽  
Vol 54 (1) ◽  
pp. 282-290 ◽  
Author(s):  
Alessandra Cristina Pedro ◽  
Fabiane Bach ◽  
Ana Paula Stafussa ◽  
Leociley Rocha Alencar Menezes ◽  
Andersson Barison ◽  
...  

1982 ◽  
Vol 84 (12) ◽  
pp. 468-472 ◽  
Author(s):  
E. M. Gaydou ◽  
Dr. J.-P. Bianchini ◽  
A. Ralaimanarivo

Foods ◽  
2020 ◽  
Vol 9 (7) ◽  
pp. 901
Author(s):  
Veronica Lolli ◽  
Pablo G. Toral ◽  
Augusta Caligiani ◽  
Pilar Gómez-Cortés

Cyclopropenoid fatty acids (CPEFA), found in oilseeds from Malvaceae and Sterculiaceae, have been shown to interfere with the endogenous synthesis of several bioactive lipids of dairy fat, such as cis-9, trans-11 18:2 and cis-9 18:1, by inhibiting Δ9-desaturase. No previous study has reported the presence of sterculic acid in animal fat and its incorporation in tissues after its administration, due to the lack of a proper methodology. In the present research, a GC-MS method based on cold base derivatization to fatty acids methylesters was developed to determine CPEFA in ewe milk triglycerides, after infusing sterculic acid (0.5 g/day) to six lactating ewes. An alternative derivatization based on silanyzation followed by GC-MS analysis was also tested, showing its possible applicability when CPEFA are present in the form of free fatty acids. Sterculic acid was detected in ewe milk triglycerides, demonstrating its incorporation from the bloodstream into milk by the mammary gland. The mean transfer rate represented 8.0 ± 1.0% of the daily dose. This study provides, for the first time, the presence of sterculic acid in milk fat, supporting the importance of understanding its occurrence in vivo and encouraging further research to determine whether it can be present in foods, such as dairy products, obtained under practical farming conditions.


2018 ◽  
Vol 5 (12) ◽  
pp. 181483 ◽  
Author(s):  
Lauren E. Jamieson ◽  
Angela Li ◽  
Karen Faulds ◽  
Duncan Graham

Raman spectroscopy has been used extensively for the analysis of biological samples in vitro , ex vivo and in vivo . While important progress has been made towards using this analytical technique in clinical applications, there is a limit to how much chemically specific information can be extracted from a spectrum of a biological sample, which consists of multiple overlapping peaks from a large number of species in any particular sample. In an attempt to elucidate more specific information regarding individual biochemical species, as opposed to very broad assignments by species class, we propose a bottom-up approach beginning with a detailed analysis of pure biochemical components. Here, we demonstrate a simple ratiometric approach applied to fatty acids, a subsection of the lipid class, to allow the key structural features, in particular degree of saturation and chain length, to be predicted. This is proposed as a starting point for allowing more chemically and species-specific information to be elucidated from the highly multiplexed spectrum of multiple overlapping signals found in a real biological sample. The power of simple ratiometric analysis is also demonstrated by comparing the prediction of degree of unsaturation in food oil samples using ratiometric and multivariate analysis techniques which could be used for food oil authentication.


1974 ◽  
Vol 31 (8) ◽  
pp. 1397-1400 ◽  
Author(s):  
Y. Malevski ◽  
J. H. Wales ◽  
M. W. Montgomery

Histological changes in livers of rainbow trout (Salmo gairdneri) repeatedly fed diets containing cyclopropenoid fatty acids (CPFA) revealed that these fish were unable to develop resistance to liver damage caused by CPFA. One group of trout was fed 150 ppm CPFA in the basal diet for 49 days followed by the basal diet for the remainder of the experimental period. Another group of trout was fed 150 ppm CPFA for 49 days, basal diet for 65 days, and 150 ppm CPFA for 45 days. At this time this group was divided into two subgroups; one received basal diet for 15 days, the other for 30 days, after which both subgroups were placed on a diet containing 360 ppm CPFA for 36 days. Analysis of the livers for histological changes showed that the parenchymal cells underwent cyclic changes of injury and recovery each time the trout were fed CPFA. Complete recovery of parenchymal cells occurred after the fish were removed from the diets containing CPFA for 30 days. Bile duct and blood vessel hyperplasia was observed for as long as 7 mo after CPFA was eliminated from the trout diet.


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