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Recent Advances in Analytical Techniques for Fructooligosaccharides in Foods
LI Xiu-ying, HUANG Jin-feng, XIAN Yan-ping, HOU Xiang-chang, LIN Sen-yu, GUO Xin-dong
Journal of Dairy Science and Technology    2014, 37 (3): 31-34.   DOI: 10.15922/j.cnki.jdst.2014.03.009
Abstract100)   HTML0)    PDF (1302KB)(18)       Save
Fructooligosaccharides (FOS) have multiple physiological functions. As the range of their application in the food industry as a novel food additive has been increasingly broadened, it is necessary to monitor added FOS in foods by means of modern analytical approaches. This paper reviews several analytical techniques that have been recently developed to determine FOS in foods, including high performance liquid chromatography, ion chromatography, matrix-assisted laser desorption ionization-mass spectrometry and gas chromatography-mass spectrometry. The advantages and disadvantages of these techniques are summarized to provide valuable references for efficient and rapid determination of FOS in foods.
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Quick Determination of 20 Anabolic Hormones in Milk and Milk Powder by LC-MS-MS
CAI Wei-hong, HE Min-heng, LI Xiu-ying, HUANG Jin-feng, DU Wei-feng, LI Pei-si, XIAN Yan-ping, HOU Xiang-chang, GUO Xin-dong
Journal of Dairy Science and Technology    2014, 37 (3): 8-12.   DOI: 10.15922/j.cnki.jdst.2014.03.003
Abstract92)   HTML0)    PDF (1558KB)(21)       Save
A quick confirmative method for the determination of residual amounts of 11 anabolic hormones and 9 agonists in milk and milk powder by liquid chromatography-tandem mass spectrometry (LC-MS-MS) was developed. Samples were extracted with acetonitrile containing 0.1% formic acid by volume. After lipid removal by liquid-liquid extraction with n-hexane, the purification of the extract was carried out on an Oasis HLB cartridge by solid-phase extraction. The analytes were separated on a C8 column employing a mobile phase composed of a mixture of methanol with 0.1% formic acid and 0.1% formic for gradient elution. The tandem mass spectral acquisition was done in the positive electrospray ionization mode utilizing multiple reaction monitoring. External standard method was applied for quantization. The results indicated that the limits of quantification (LOQs, RSN = 10) for 20 target compounds ranged from 0.1 to 1.0 μg/kg, and the linear range was 0.05–50 μg/L with correlation coefficients larger than 0.996. The average recoveries at different spiked concentration levels ranged from 52.8% to 97.4% with RSD of 2.8%–9.6% (n = 6). The proposed method has been applied for the rapid determination of real samples of milk and milk powder with simple operation and accurate results.
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