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1.
J Oleo Sci ; 59(2): 71-9, 2010.
Article in English | MEDLINE | ID: mdl-20103979

ABSTRACT

The characteristics of a non-endcapped polymeric ODS column for the resolution of triacylglycerol positional isomers (TAG-PI) were examined using a recycle HPLC-atmospheric pressure chemical ionization/mass spectrometry system. A pair of TAG-PI containing saturated fatty acids at least 12 carbons was separated. Except for TAG-PI containing elaidic acid, pairs of TAG-PI containing three unsaturated fatty acids were not separated, even by recycle runs. These results indicate that the resolution of TAG-PI on a non-endcapped polymeric ODS stationary phase is realized by the recognition of the linear structure of the fatty acid and the binding position of the saturated fatty acid in TAG-PI. Chain length was also an important factor for resolution. This method may be a useful and simple for measuring the abundance ratio of TAG-PI containing saturated fatty acids in natural oils.


Subject(s)
Chromatography, High Pressure Liquid/instrumentation , Polymers/chemistry , Silicon Dioxide/chemistry , Triglycerides/isolation & purification , Isomerism , Triglycerides/chemistry
2.
J Agric Food Chem ; 55(26): 11052-6, 2007 Dec 26.
Article in English | MEDLINE | ID: mdl-18038996

ABSTRACT

Lipid oxidation in dispersed lipids is prevalent at the oil-water interface where lipid hydroperoxides are decomposed into free radicals by transition metals. Free radical scavenging antioxidants are believed to be most effective in lipid dispersions when they accumulate at the oil-water interface. The surface activity of antioxidants could be increased by their conjugation to hydrocarbon chains. In this study, p-hydroxyphenylacetic acid (HPA) was conjugated with either a butyl or dodecyl group. The HPA conjugates were more effective at decreasing interfacial tension than unconjugated HPA, indicating that they were able to adsorb at lipid-water interfaces. However, free HPA was a more effective antioxidant than butyl and dodecyl conjugates in Menhaden oil-in-water emulsions as determined by both lipid hydroperoxides and thiobarbituric acid reactive substances. The increased antioxidant activity of free HPA could be due to its more effective free radical scavenging activity and its higher concentration in the lipid phase of oil-in-water emulsions in the presence of surfactant micelles where it can act as a chain-breaking antioxidant.


Subject(s)
Antioxidants/pharmacology , Emulsions/chemistry , Lipid Peroxidation/drug effects , Surface-Active Agents/pharmacology , Fish Oils , Phenylacetates/chemistry , Phenylacetates/pharmacology , Surface-Active Agents/chemistry , Water
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