scholarly journals Corrigendum to “Chemometric studies of the effects of milk fat replacement with different proportions of vegetable oils in the formulation of fat-filled milk powders: Implications for quality assurance” [Food Chem. 295 (2019) 198–205]

2020 ◽  
Vol 308 ◽  
pp. 125541
Author(s):  
Kizito Kene Ejeahalaka ◽  
Stephen L.W. On
2020 ◽  
Vol 99 (5) ◽  
pp. 2811-2818
Author(s):  
Dong-Jin Shin ◽  
Hyun Jung Lee ◽  
Dongheon Lee ◽  
Cheorun Jo ◽  
Juhui Choe

2022 ◽  
Vol 34 (2) ◽  
pp. 429-431
Author(s):  
A.I. Kozhushkevich ◽  
E.S. Kozeicheva ◽  
A.M. Lebedev ◽  
V.V. Ovcharenko ◽  
A.M. Kalantaenko

Due to the increasing globalization of food markets, there are evolving new challenges for maintaing food safety. The current problem is the development of analytical methods for 3-monochloropropanediol ester and glycidol ester, which are food contaminants of concern for the scientific community. The levels of 3-monochloropropanediol ester and glycidol ester in certain food products are controlled by the European legislation. However, the maximum allowed concentrations and uptake limits for various food products are permanently revised. Therefore, we aimed to determine 3-monochloropropanediol ester and glycidol ester in various food products, which may contain vegetable oils. We analyzed food samples obtained from local food shops, predominantly low-priced products, which are more likely to contain vegetable oils, and adulterated milk fat. The levels of 3-monochloropropanediol ester and glycidol ester were determined indirectly by analyzing free 3-monochloropropanediol and glycidol ester obtained by hydrolysis and derivatized with phenylboronic acid. Samples were analyzed by GC-MS/MS on a triple-quad mass spectrometer.


1979 ◽  
Vol 62 (4) ◽  
pp. 709-721
Author(s):  
David Firestone ◽  
William Horwitz

Abstract An international collaborative study of IUPAC methods II.D.19 and II.D.25 for preparation and GLC analysis of fatty acid methyl esters was begun in 1976. The IUPAC methodology, applicable to animal and vegetable oils and fats and fatty acids from all sources, contains special instructions for preparation and analysis of methyl esters of fatty acids containing 4 or more carbon atoms (analysis of milk fat). Twenty-three collaborators participated in the analysis of 5 known mixtures, 4 vegetable oils, 1 fish oil, and 2 butterfats. Several blind duplicate samples were included. The experimental data were subjected to statistical analysis to examine intra- and interlaboratory variation. Reproducibility and accuracy data for the higher fatty acid (14:0–22:1) mixtures and fish and vegetable oils were satisfactory and were in good agreement with results from an AOCS Smalley Committee check sample program involving analysis of the same samples. Typical coefficients of variation (%) at various concentrations were 15 (2% level), 8.5 (5% level), 7 (10% level), and 3 (50% level). Low recoveries and poor reproducibility were characteristic of results obtained for butyric acid in the butterfat and related known mixtures. A coefficient of variation of about 19% was found for analysis of butyric acid in butterfat, vs. coefficients of variation in the range of 4–13% for similar levels of other components in butterfat and other samples. The IUPAC methodology for GLC analysis .of fats and oils other than milk fats has been adopted by the AOAC as official first action to replace the current GLC method, 28.063-28.067.


2018 ◽  
Vol 55 (3) ◽  
pp. 858-867 ◽  
Author(s):  
Mariana B. Osuna ◽  
Ana M. Romero ◽  
Carmen M. Avallone ◽  
María A. Judis ◽  
Nora C. Bertola

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