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

Author:

Turner T.1,Rolland D.C1,Aldai N.2,Dugan M. E. R.1

Affiliation:

1. Agriculture and Agri-Food Canada, Lacombe Research Centre, 6000 C & E Trail Lacombe, Alberta, Canada T4L 1W1

2. Instituto de Ganadería de Montaña (Consejo Superior de Investigaciones Científicas, Universidad de León), Finca Marzanas, E-24346 Grulleros, León, Spain

Abstract

Turner, T., Rolland, D. C., Aldai, N. and Dugan, M. E. R. 2011. Short Communication: Rapid separation of cis 9, trans 11- and trans 7,c is 9-18:2 (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°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).

Publisher

Canadian Science Publishing

Subject

Animal Science and Zoology,Food Animals

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