scholarly journals A New Analytical Method for the Quantification of Glycidol Fatty Acid Esters in Edible Oils

2010 ◽  
Vol 59 (2) ◽  
pp. 81-88 ◽  
Author(s):  
Yoshinori Masukawa ◽  
Hiroki Shiro ◽  
Shun Nakamura ◽  
Naoki Kondo ◽  
Norikazu Jin ◽  
...  
2013 ◽  
Vol 30 (1) ◽  
pp. 52-68 ◽  
Author(s):  
K. Yamazaki ◽  
M. Ogiso ◽  
S. Isagawa ◽  
T. Urushiyama ◽  
T. Ukena ◽  
...  

2013 ◽  
Vol 30 (2) ◽  
pp. 412-412 ◽  
Author(s):  
K. Yamazaki ◽  
M. Ogiso ◽  
S. Isagawa ◽  
T. Urushiyama ◽  
T. Ukena ◽  
...  

2017 ◽  
Vol 409 (17) ◽  
pp. 4267-4278 ◽  
Author(s):  
Renata Jędrkiewicz ◽  
Agnieszka Głowacz-Różyńska ◽  
Justyna Gromadzka ◽  
Piotr Konieczka ◽  
Jacek Namieśnik

2019 ◽  
Vol 102 (4) ◽  
pp. 1205-1220 ◽  
Author(s):  
Jan Kuhlmann

Abstract Background: Fatty acid esters of glycidol, 2-Monochloropropanediol (MCPD), and 3-MCPD are heat-induced foodborne processing contaminants with possible adverse health effects. These compounds occur frequently in refined edible oils. Consequently, glycidyl esters and 2- and 3-MCPD esters might also be present in foods that contain refined edible oils. Objective: This manuscript describes the single-laboratory validation of an analytical method for the quantitative determination of glycidol, 2-MCPD, and 3-MCPD present as fatty acid esters or as free 2- or 3-MCPD in infant and adult/pediatric nutritional formula. Methods: Technically, the presented method is based on the combination of a Heat-Ultrasound Pressure-supported Solvent Extraction and a GC–MS determination of glycidol, 2-MCPD, and 3-MCPD. From a chemical perspective, the method includes an alkaline catalyzed transesterification, conversion of the unstable glycidol into monobromopropanediol, and the parallel derivatization of all analytes with phenylboronic acid. Results: Validation results showed that method linearity for all analytes in powdered and liquid infant formula ranged from 0.9981 to 0.9999 (n = 18). Repeatability relative standard deviation values for concentration levels between 1.3 μg/kg and 331 μg/kg were in the range of 1 to 12%. Relative recoveries were found to be between 93 and 107%. The analytes were quantifiable down to 5–10 μg/kg in powdered samples and 1–2 μg/kg in liquid samples. Conclusions: The reported results met actual AOAC Standard Method Performance Requirements. Highlights: In terms of consumer protection, the presented method is a novel approach for the sensitive and accurate determination of glycidol, 2-MCPD, and 3-MCPD in infant formula and related foodstuffs.


2011 ◽  
Vol 113 (3) ◽  
pp. 356-360 ◽  
Author(s):  
Hiroki Shiro ◽  
Naoki Kondo ◽  
Nobuyuki Kibune ◽  
Yoshinori Masukawa

2013 ◽  
Vol 30 (1) ◽  
pp. 46-51 ◽  
Author(s):  
B.D. Craft ◽  
A. Chiodini ◽  
J. Garst ◽  
M. Granvogl

2012 ◽  
Vol 90 (4) ◽  
pp. 493-500 ◽  
Author(s):  
Michael R. Blumhorst ◽  
Mark W. Collison ◽  
Richard Cantrill ◽  
Hiroki Shiro ◽  
Yoshinori Masukawa ◽  
...  

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