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The Analytical Scientist / App Notes / 2018 / Simple, Rapid Detection of Edible Oil Oxidation Using Direct MS

Simple, Rapid Detection of Edible Oil Oxidation Using Direct MS

03/19/2018

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Process-line or laboratory detection of edible oil oxidation is achieved extremely simply by applying selected ion flow tube mass spectrometry (SIFT-MS). Direct headspace analysis of fish oil using SIFT-MS enables instantaneous quantification of volatile oxidation markers.

Edible oils rich in unsaturated fatty acids offer health benefits, but they are susceptible to autoxidation, which compromises product flavor and shortens its shelf-life. Generally, greater unsaturation in the fatty acid chain means more extensive autoxidation will occur in a given time. Autoxidation produces volatile aldehydes, ketones, and saturated and unsaturated hydrocarbons providing sensitive indicators of oxidative status for instrumental methods. Traditional methods for fish oils have targeted propanal, but application of SIFT-MS enables other confirmatory volatiles to be detected simultaneously.In this study, five 1-mL fish oil capsules (“Giant Eagle” brand, USA) were placed in duplicate wide-mouthed sample jars. Capsules were opened inside the jars, and the contents allowed to drain. Jars were capped immediately (trapping laboratory air) and left on a laboratory bench at ambient temperature for the duration of the tests (diurnal variation from 12 to 25 °C). Figure 1 shows the propanal concentration measured for fish oil samples and blanks over a four-day period. The “Day 0” measurements were made one hour after the samples were prepared (i.e. on the freshly cut capsules) and reveal a significant concentration of propanal in the “fresh” oil (22 parts-per-billion by volume; ppbv).

Figure 1. The propanal concentration as measured using the NO+ reagent ion of SIFT-MS.

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