4.1 Article

SHORT COMMUNICATION: Rapid separation of cis9, trans11- and trans7,cis9-18:2 (CLA) isomers from ruminant tissue using a 30 m SLB-IL111 ionic column

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CANADIAN JOURNAL OF ANIMAL SCIENCE
卷 91, 期 4, 页码 711-713

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AGRICULTURAL INST CANADA
DOI: 10.4141/CJAS2011-071

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Biohydrogenation; conjugated linoleic acid; gas chromatography

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Turner, T., Rolland, D. C., Aldai, N. and Dugan, M. E. R. 2011. SHORT COMMUNICATION: Rapid separation of cis9,trans11- and trans7,cis9-18:2 (CLA) isomers from ruminant tissue using a 30 m SLB-IL111 ionic column. Can. J. Anim. Sci. 91: 711-713. Rumenic acid (cis9,trans11-18:2) is the main natural isomer of conjugated linoleic acid (CLA). Rumenic acid has many purported health benefits, but effects of most other CLA isomers are unknown. Typically trans7,cis9-18:2 is the second most abundant CLA isomer, but it co-elutes with rumenic acid on conventional polar gas chromatography (GC) columns, requiring complimentary analysis with silver-ion high performance liquid chromatography (Ag(+)-HPLC). Herein we report a rapid method for analyzing rumenic acid and trans7,cis9-18:2 using a 30 m ionic-liquid GC column. Optimal resolution of the two CLA isomers was at 145 degrees C and analysis of backfat from barley-fed cattle compared well with GC/Ag(+)-HPLC (y =0.978x - 0.031, r =0.985, P <0.001).

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