Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7599324 | Food Chemistry | 2014 | 7 Pages |
Abstract
Direct determination of free cordycepin in designer egg using a highly selective mass spectrometric (MS) technique aided by a rapid and efficient dilute-and-shoot workflow would enhance their application as diagnostic tools in food fraud control. Here, triple stage mass spectrometry (MS3) demonstrated excellent analyte selectivity capability even when incomplete chromatographic separation was performed. Method validation was performed at six concentration levels of 100, 200, 400, 800, 1200 and 1600 ng gâ1. Spiking experiments were examined at three concentration levels of 200, 400, and 1200 ng gâ1 in individual egg white and egg yolk, measured over 2 days. MS3 enabled ion chromatograms with zero-background interference to be made in egg extracts. MS3 eliminated severe over recovery (p < 0.05) observed in all fortified samples, a challenge that MRM-transition could not address in a single step. Matrix-matched calibrants were needed to compensate for over recovery observed under MRM-transition mode.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Yi Hsin Chen, Chee Wei Lim, Sheot Harn Chan,